Aminoadipate-semialdehyde synthase (AASS) irna compositions and methods of use thereof

Abstract

The invention relates to double-stranded ribonucleic acid (dsRNA) compositions targeting the AASS gene, as well as methods of inhibiting expression of AASS, and methods of treating subjects that would benefit from reduction in expression of AASS, such as subjects having an AASS-associated disease, disorder, or condition, using such dsRNA compositions.

Description

[0001] AMINOADIPATE-SEMIALDEHYDE SYNTHASE (AASS) iRNA COMPOSITIONS AND METHODS OF USE THEREOF

[0002] CROSS-REFERENCE TO RELATED APPLICATIONS

[0003] This application claims the benefit of priority to U.S. Provisional Application No. 63 / 672, 129, filed on July 16, 2024. and to U.S. Provisional Application No. 63 / 517,811, filed on August 4, 2023. The entire contents of the foregoing applications are hereby incorporated herein by reference.

[0004] FIELD OF THE INVENTION

[0005] The instant disclosure relates generally to aminoadipate-semialdehyde synthase (AASS)-targeting dsRNA agents and methods for their use.

[0006] SEQUENCE LISTING

[0007] The instant application contains a Sequence Listing which has been filed electronically in extensible Markup Language (XML) format and is hereby incorporated by reference in its entirety. Said XML copy, created on August 1, 2024, is named A108868_1730WO_SL.xml and is 63,031,180 bytes in size.

[0008] BACKGROUND OF THE INVENTION

[0009] Lysine is an essential amino acid involved in protein synthesis, production of carnitine, and enzyme catalysis. The most common pathway of lysine catabolism is the saccharopine pathway which mainly occurs in liver mitochondria and leads to the production of acetyl-CoA. The first two reactions in the saccharopine pathway are catalyzed by aminoadipate-semialdehyde synthase (AASS), a bifiinctional enzyme which possesses both lysine-ketoglutarate reductase and saccharopine dehydrogenase activities leading to the production of glutaryl -coenzyme A (glutaryl-CoA). The Glutaryl-CoA dehydrogenase (GCDH) enzyme catalyzes the reaction of glutaryl-CoA to crotonyl-CoA. Inhibition of the conversion of glutaryl- CoA to crotonyl-CoA leads to the production and accumulation of toxic catabolites such as glutaric acid and 3 -hydroxy-glutaric acid.

[0010] An alternative lysine catabolism pathway is the pipecolate pathway which occurs mainly in the adult brain and converges into a common degradation pathway with the saccharopine pathway at the step catalyzed by the enzyme a-aminoadipic semialdehyde dehydrogenase (ALDH7A1).

[0011] Disruptions of the lysine catabolism pathways result can result in various disorders. At least two severe neurometabolic disorders, glutaric aciduria type 1 (GAI) and pyridoxine-dependent epilepsy (PDE) are associated with mutations in lysine catabolism enzymes. GAI is caused by a deficiency in the GCDH enzyme and PDE is caused by mutations in the ALDH7A1 enzyme. Deficiency in GCDH causes inhibition of the conversion of glutaryl-CoA to crotonyl-CoA and leads to the production and accumulation of toxic catabolites such as glutaric acid and 3-hydroxy-glutaric acid. Accumulation of these catabolites leads to encephalopathic crisis, striatal brain injury, and severe movement disorder. ALDH7A1 deficiency leads to the accumulation of L-Pipecolic acid resulting in seizures from infancy, intellectual disability, and neurologic abnormalities. The AASS enzyme is upstream of both the GCDH and ALDH7A1 enzymes in the lysine catabolism pathway and represents a potential therapeutic target in lysine catabolism disorders.

[0012] Accordingly, there is a need for methods of treating disorders of lysine catabolism, such as GA 1 and PDE, including agents that can selectively and efficiently inhibit the AASS gene.

[0013] BRIEF SUMMARY OF THE INVENTION

[0014] There is a need for improved methods of treating lysine catabolism disorders, such as glutaric aciduria type 1 (GAI) and pyridoxine -dependent epilepsy (PDE), including agents that can selectively and efficiently inhibit the AASS gene. Current standards of care for subjects with lysine catabolism disorders include low lysine diet, carnitine supplementation, emergency treatment (ET) during illness, fasting, and / or pyridoxine administration.

[0015] The present invention provides iRNA compositions which effect the RNA-induced silencing complex (RlSC)-mcdiatcd cleavage of RNA transcripts of a Aminoadipatc-scmialdchydc synthase (AASS) gene. The AASS gene may be within a cell, e.g., a cell within a subject, such as a human. Tire present invention also provides methods of using the iRNA compositions of the invention for inhibiting the expression of an AASS gene and / or for treating a subject who would benefit from inhibiting or reducing the expression of an AASS gene, e.g., a subject suffering or prone to suffering from an AASS-associated disease, for example, a lysine catabolism disorder.

[0016] Accordingly, in one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of Aminoadipate -semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand and an antisense strand, wherein the sense strand comprises at least 15 contiguous nucleotides differing by no more than 1, 2, or 3 nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 1, 2, or 3 nucleotides from the nucleotide sequence of SEQ ID NO: 2. In some embodiments, the dsRNA agent includes a sense strand and an antisense strand, wherein the sense strand comprises at least 15 contiguous nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides from the nucleotide sequence of SEQ ID NO: 2.

[0017] In another aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand and an antisense strand forming a double stranded region, wherein said antisense strand comprises a region of complementarity to an mRNA encoding AASS which comprises at least 15 contiguous nucleotides differing by no more than 1, 2. or 3 nucleotides from any one of the antisense sequences listed in any one of Tables 3-6. In some embodiments, the dsRNA agent includes a sense strand and an antisense strand forming a double stranded region, wherein said antisense strand comprises a region of complementarity to an mRNA encoding AASS which comprises at least 15 contiguous nucleotides from any one of the antisense sequences listed in any one of Tables 3-6.

[0018] In another embodiment, the region of complementarity comprises at least 15 contiguous nucleotides differing by no more than 1. 2, or 3 nucleotides from any one of nucleotides 381-403, 746- 768, 747-769, 263-285, 2465-2487, 248-270, 249-271, 251-273, 254-276, 255-277, 256-278, 258-280, 260-282, 263-285, 266-288, 272-294, 273-295, 274-296, 275-297, 276-298, 278-300, 279-301, 280-302,

[0019] 281-303, 284-306, 285-307, 288-310, 289-311, 291-313, 309-331, 312-334, 313-335, 314-336, 315-337,

[0020] 316-338, 317-339, 318-340, 319-341, 320-342, 321-343, 322-344, 323-345, 324-346, 325-347, 326-348,

[0021] 327-349, 328-350. 329-351, 330-352, 333-355, 334-356, 336-358, 337-359. 339-361, 348-370, 349-371,

[0022] 999-1021. 3004-3026. 3005-3027. 2903-2925, 2319-2341, 2905-2927, 360-382. 361-383. 362-384, 363- 385, 364-386, 365-387, 366-388, 367-389, 368-390, 369-391, 370-392, 371-393, 372-394, 373-395, 374-

[0023] 396, 375-397, 376-398, 377-399, 378-400, 381-403, 383-405, 384-406, 385-407, 386-408, 387-409, 388-

[0024] 410, 389-411, 397-419, 398-420, 399-421, 400-422, 401-423, 402-424, 403-425, 404-426, 405-427, 406-

[0025] 428, 407-429, 408-430, 409-431, 410-432, 411-433, 412-434, 413-435, 416-438, 417-439, 418-440, 419-

[0026] 441. 420-442, 421-443, 422-444, 423-445, 3232-3254, 3233-3255, 426-448, 3235-3257, 3236-3258, 429- 451. 430-452, 431-453, 432-454, 433-455, 434-456. 435-457. 436-458, 437-459, 438-460, 440-462, 444-

[0027] 466, 445-467, 446-468, 448-470, 449-471, 451-473, 459-481, 467-489, 472-494, 473-495, 475-497, 476-

[0028] 498, 477-499, 478-500, 479-501, 480-502, 481-503, 482-504, 483-505, 484-506, 485-507, 486-508, 487-

[0029] 509, 488-510, 489-511, 490-512, 491-513, 492-514, 493-515, 494-516, 495-517, 496-518, 498-520, 423-

[0030] 445, 500-522, 501-523, 502-524, 503-525, 504-526, 505-527, 506-528, 507-529, 508-530, 509-531, 510-

[0031] 532. 511-533, 512-534, 513-535, 514-536, 515-537. 516-538, 517-539, 518-540, 520-542, 521-543, 522-

[0032] 544. 523-545, 524-546, 525-547, 526-548, 527-549. 528-550. 530-552, 531-553, 534-556, 535-557, 580-

[0033] 602, 581-603, 582-604, 583-605, 584-606, 585-607, 586-608, 587-609, 588-610, 589-611, 590-612, 591-

[0034] 613, 592-614, 593-615, 594-616, 595-617, 596-618, 597-619, 598-620, 599-621, 600-622, 601-623, 603-

[0035] 625, 605-627, 609-631, 610-632, 613-635, 614-636, 617-639, 618-640, 634-656, 636-658, 637-659, 639-

[0036] 661, 640-662, 641-663, 642-664, 643-665, 646-668, 647-669, 650-672, 651-673, 654-676, 659-681, 660-

[0037] 682. 662-684, 663-685, 669-691, 670-692, 671-693. 674-696, 675-697, 678-700, 715-737, 716-738, 717-

[0038] 739. 720-742. 721-743, 722-744, 723-745, 724-746. 725-747. 726-748, 727-749, 728-750, 734-756, 737-

[0039] 759, 740-762, 741-763, 745-767, 751-773, 754-776, 755-777, 756-778, 757-779, 761-783, 762-784, 763-

[0040] 785, 764-786, 765-787, 766-788, 767-789, 769-791, 770-792, 776-798, 778-800, 780-802, 781-803, 783-

[0041] 805, 785-807, 786-808, 788-810, 789-811, 790-812, 792-814, 808-830, 809-831, 811-833, 812-834, 813-

[0042] 835, 815-837, 816-838, 817-839, 818-840, 825-847. 826-848, 828-850, 829-851, 831-853, 832-854, 833-

[0043] 855. 855-877, 856-878, 857-879, 859-881, 860-882. 861-883, 862-884, 877-899, 878-900, 882-904, 884- 906, 887-909, 891-913, 895-917, 896-918, 898-920, 899-921, 901-923, 902-924, 904-926, 906-928, 907-

[0044] 929, 908-930, 909-931, 910-932, 912-934, 913-935, 915-937, 916-938, 918-940, 920-942, 921-943, 922-

[0045] 944, 923-945, 925-947, 926-948, 927-949, 928-950, 929-951, 931-953, 932-954, 933-955, 936-958, 937-

[0046] 959, 939-961, 940-962, 941-963, 943-965, 944-966, 948-970, 951-973, 2868-2890, 319-341, 2933-2955,

[0047] 2934-2956, 2935-2957, 2936-2958, 2937-2959, 2938-2960, 979-1001, 983-1005, 984-1006, 985-1007, 986-1008. 987-1009, 988-1010, 989-1011, 990-1012, 991-1013, 992-1014, 993-1015. 994-1016, 998- 1020, 999-1021, 1005-1027, 1012-1034, 1017-1039, 1018-1040, 1019-1041, 1020-1042, 1021-1043, 1022-1044, 1028-1050, 1029-1051, 1032-1054, 1039-1061, 1042-1064, 1044-1066, 1046-1068, 1083- 1105, 1084-1106, 1091-1113, 1144-1166, 1145-1167, 1147-1169, 1150-1172, 1154-1176, 1157-1179, 1160-1182, 1161-1183, 1162-1184, 1163-1185, 1165-1187, 1166-1188, 1167-1189, 1168-1190, 1169- 1191, 1170-1192, 1171-1193, 1172-1194, 1173-1195, 1174-1196. 1175-1197. 1176-1198, 1193-1215, 1194-1216, 1195-1217, 1196-1218, 1197-1219, 1198-1220. 1199-1221. 1200-1222. 1201-1223. 1202- 1224, 1203-1225, 1204-1226, 1205-1227, 1206-1228, 1227-1249, 1228-1250, 1229-1251, 1230-1252, 1233-1255, 1234-1256, 1235-1257, 1236-1258, 1237-1259, 1238-1260, 1239-1261, 1240-1262, 1241- 1263, 1242-1264, 1243-1265, 1244-1266, 1245-1267, 1248-1270, 1253-1275, 1255-1277, 1257-1279, 1260-1282, 1262-1284, 1263-1285, 1264-1286, 1265-1287, 1266-1288, 1268-1290, 1269-1291. 1270- 1292, 1273-1295, 1275-1297, 1277-1299, 1278-1300, 1301-1323. 1302-1324. 1303-1325, 1304-1326, 1305-1327, 1306-1328, 1307-1329, 1308-1330, 1309-1331. 1310-1332. 1311-1333. 1312-1334. 1313- 1335, 1314-1336, 1316-1338, 1334-1356, 1336-1358, 1338-1360, 1339-1361, 1340-1362, 2496-2518, 2497-2519, 2498-2520, 2499-2521, 1345-1367, 1346-1368, 1348-1370, 1349-1371, 1350-1372, 1351- 1373, 1352-1374, 1353-1375, 1356-1378, 1357-1379, 1358-1380, 1359-1381, 1360-1382, 1361-1383, 1362-1384, 1364-1386, 1365-1387, 1366-1388, 1367-1389, 1368-1390, 1369-1391, 1370-1392. 1371- 1393, 1372-1394, 1373-1395, 1374-1396, 1375-1397, 1376-1398. 1377-1399. 1378-1400, 1379-1401, 1380-1402, 1381-1403, 1382-1404, 3161-3183, 1390-1412. 1391-1413. 1392-1414. 1412-1434. 1413- 1435, 1414-1436, 1415-1437, 1416-1438, 1417-1439, 1418-1440, 1419-1441, 1420-1442, 1421-1443, 1422-1444, 1423-1445, 1424-1446, 1425-1447, 3572-3594, 3573-3595, 3082-3104, 1431-1453, 1447- 1469, 1449-1471, 1450-1472, 1451-1473, 1453-1475, 1454-1476, 1455-1477, 1456-1478, 1459-1481, 1460-1482, 2261-2283, 2476-2498, 1731-1753, 3576-3598, 1473-1495, 1474-1496, 1475-1497. 1476- 1498, 1477-1499, 1478-1500, 1495-1517, 1496-1518, 1497-1519. 1498-1520. 1499-1521, 1500-1522, 1501-1523, 1502-1524, 2144-2166, 1528-1550, 1532-1554. 1534-1556. 1537-1559. 1538-1560. 1550- 1572, 1556-1578, 1557-1579, 1558-1580, 1559-1581, 1562-1584, 1563-1585, 1569-1591, 1570-1592, 1572-1594, 1573-1595, 1576-1598, 1583-1605, 1584-1606, 1585-1607, 1586-1608, 1590-1612, 1591- 1613, 1594-1616, 1595-1617, 1596-1618, 1597-1619, 1598-1620, 1599-1621, 1600-1622, 1938-1960, 1157-1179, 1615-1637, 1616-1638, 1617-1639, 1618-1640, 1619-1641, 1620-1642, 1621-1643. 1622- 1644, 1623-1645, 1624-1646, 1625-1647, 1626-1648. 1627-1649. 1628-1650. 1629-1651, 1633-1655, 1634-1656, 1638-1660, 1639-1661, 1641-1663, 1642-1664, 1643-1665, 2965-2987, 3048-3070, 3049- 3071, 3050-3072, 1649-1671, 1650-1672, 1651-1673, 3241-3263, 3242-3264, 2773-2795, 2774-2796, 2858-2880, 1864-1886, 2652-2674, 2653-2675, 3634-3656, 1669-1691, 1670-1692, 1671-1693, 1672- 1694, 1673-1695, 1674-1696, 1675-1697, 1676-1698, 2651-2673, 2652-2674, 97- 119, 3174-3196, 3175- 3197, 3176-3198, 3314-3336, 3290-3312, 3291-3313, 3292-3314. 1709-1731. 1710-1732, 490-512, 1543- 1565, 1544-1566, 414-436, 1509-1531, 1510-1532, 851-873, 2436-2458, 1720-1742, 1045-1067, 1046- 1068, 1747-1769, 1749-1771, 1752-1774, 1753-1775, 1754-1776, 1755-1777, 1758-1780, 1760-1782, 1761-1783, 1763-1785, 1765-1787, 1766-1788, 1768-1790, 1769-1791, 1771-1793, 1772-1794, 1773- 1795, 3130-3152, 3622-3644, 3623-3645, 1804-1826, 171-193, 172-194, 1814-1836, 1815-1837, 1681- 1703, 1817-1839, 1818-1840, 1820-1842, 1821-1843, 1823-1845, 1824-1846, 1826-1848, 1829-1851, 1833-1855, 1838-1860, 1840-1862, 1841-1863, 1844-1866, 1850-1872, 1852-1874. 443-465, 1854-1876, 1855-1877, 1856-1878, 1857-1879, 1858-1880, 1859-1881. 1860-1882. 1861-1883. 1862-1884. 1863- 1885, 1864-1886, 1865-1887, 1866-1888, 1867-1889, 1868-1890, 1869-1891, 1870-1892, 1871-1893, 1872-1894, 1873-1895, 1874-1896, 1875-1897, 1876-1898, 1877-1899, 1878-1900, 1884-1906, 1887- 1909, 1888-1910, 1891-1913, 1892-1914, 1893-1915, 1895-1917, 1898-1920, 1900-1922, 1901-1923, 1902-1924, 1907-1929, 1908-1930, 1909-1931, 1912-1934, 1930-1952, 1931-1953, 1932-1954. 1933- 1955, 1934-1956, 1935-1957, 1936-1958, 1937-1959, 1938-1960. 1939-1961. 1940-1962, 1941-1963, 1942-1964, 1943-1965, 1944-1966, 1945-1967, 1946-1968. 1947-1969. 1948-1970. 1949-1971. 1950- 1972, 1951-1973, 1952-1974, 1953-1975, 1954-1976, 1955-1977, 1956-1978, 1957-1979, 1958-1980, 1959-1981, 1960-1982, 1961-1983, 1962-1984, 1963-1985, 800-822, 2445-2467, 1985-2007, 1986-2008, 1987-2009, 1988-2010, 1989-2011, 1990-2012, 1991-2013, 1992-2014, 1993-2015, 1994-2016, 1995- 2017, 1996-2018, 1998-2020, 1999-2021, 2000-2022, 2035-2057, 3663-3685, 2037-2059, 2038-2060, 2039-2061, 2040-2062, 2041-2063, 2042-2064, 2043-2065, 2281-2303, 2282-2304. 2283-2305. 2053- 2075, 2054-2076, 2055-2077, 2056-2078. 2057-2079. 2058-2080. 2059-2081. 2062-2084, 2078-2100, 2079-2101, 2080-2102, 2081-2103, 2083-2105, 2084-2106, 2085-2107, 2087-2109, 2088-2110, 2090- 2112, 2093-2115, 2111-2133, 2124-2146, 2126-2148, 2127-2149, 2128-2150, 2130-2152, 2133-2155, 1887-1909, 3234-3256, 13-35, 1200-1222, 2184-2206, 2185-2207, 2186-2208, 2836-2858, 2837-2859, 2192-2214, 2194-2216, 2195-2217, 2196-2218, 2197-2219, 2198-2220, 2199-2221, 2200-2222. 2205- 2227, 2206-2228, 2208-2230, 2210-2232, 2211-2233, 2212-2234. 2215-2237. 2216-2238, 2870-2892, 2871-2893, 3455-3477, 2223-2245, 2225-2247, 2226-2248. 2227-2249. 2228-2250. 2230-2252. 2231- 2253, 2232-2254, 2233-2255, 2234-2256, 2235-2257, 2236-2258, 2240-2262, 2241-2263, 2242-2264, 2243-2265, 2244-2266, 2245-2267, 2246-2268, 2248-2270, 2249-2271, 2253-2275, 1062-1084, 1066- 1088, 2259-2281, 1309-1331, 3122-3144, 1764-1786, 17-39, 2288-2310, 2289-2311, 2290-2312, 2291- 2313, 2292-2314, 2293-2315, 2295-2317, 3521-3543, 2298-2320, 2300-2322. 2301-2323, 2304-2326, 2305-2327, 2306-2328, 2307-2329, 2308-2330, 2309-2331, 2310-2332. 2311-2333. 2312-2334. 2313- 2335, 2314-2336, 2315-2337, 2316-2338, 2317-2339, 2318-2340, 2322-2344, 3244-3266, 3245-3267, 3246-3268, 3324-3346, 3325-3347, 2336-2358, 2337-2359, 2338-2360, 2340-2362, 2341-2363, 2342- 2364, 2343-2365, 973-995, 2350-2372, 2351-2373, 3310-3332, 2977-2999, 2394-2416, 2396-2418, 2397- 2419, 2399-2421, 2400-2422, 2408-2430, 2409-2431, 2411-2433, 2412-2434, 2413-2435, 2414-2436, 1915-1937, 2418-2440, 1080-1102, 1295-1317, 1298-1320, 1121-1143, 1122-1144. 1123-1145. 1376- 1398, 1125-1147, 2448-2470, 2451-2473, 483-505, 484-506, 2575-2597, 2957-2979, 3027-3049, 3028- 3050, 1494-1516, 2660-2682, 261-283, 2481-2503, 2496-2518, 2507-2529, 2509-2531, 2556-2578, 2965- 2987, 3033-3055, 2582-2604, 2583-2605, 2585-2607, 2586-2608, 2595-2617, 2598-2620, 2599-2621, 2602-2624, 2603-2625, 2604-2626, 2605-2627, 2606-2628, 2607-2629, 2608-2630, 2609-2631, 2618- 2640, 2621-2643, 2625-2647, 2627-2649, 2629-2651, 2630-2652, 2631-2653, 2632-2654, 2633-2655, 2634-2656, 2636-2658, 2637-2659, 2638-2660, 2639-2661, 2641-2663, 2642-2664. 2647-2669. 2649- 2671, 2650-2672, 2652-2674, 2653-2675, 2656-2678. 2658-2680. 2659-2681. 2660-2682, 2661-2683, 2662-2684, 2663-2685, 2664-2686, 2665-2687, 2667-2689, 2672-2694, 2673-2695, 2674-2696, 2675- 2697, 2676-2698, 2681-2703, 2682-2704, 2706-2728, 1171-1193, 2708-2730, 2716-2738, 2717-2739, 2759-2781, 2761-2783, 2762-2784, 2763-2785, 2764-2786, 2765-2787, 2766-2788, 2767-2789, 2769- 2791, 2770-2792, 2772-2794, 2773-2795, 2776-2798, 2777-2799, 2778-2800, 2779-2801, 2810-2832, 2811-2833, 2812-2834, 2813-2835, 2815-2837, 2816-2838, 2817-2839, 2818-2840. 2819-2841. 2820- 2842, 2822-2844, 2823-2845, 2824-2846. 2825-2847. 2826-2848. 2827-2849. 2828-2850, 2829-2851, 2830-2852, 2831-2853, 2832-2854, 2833-2855, 2834-2856, 2835-2857, 2836-2858, 2837-2859, 2838- 2860, 2839-2861, 2840-2862, 2841-2863, 2842-2864, 2843-2865, 2847-2869, 2848-2870, 2849-2871, 2850-2872, 2851-2873, 2852-2874, 2853-2875, 2854-2876, 2855-2877, 1487-1509, 2227-2249, 2858-

[0048] 2880, 2859-2881, 3451-3473, 2861-2883, 2862-2884, 2863-2885, 2864-2886, 2865-2887, 2866-2888, 2869-2891, 2870-2892, 2871-2893, 2872-2894, 2873-2895, 2874-2896, 2875-2897. 2876-2898. 2877- 2899, 2878-2900, 2879-2901, 2880-2902. 2881-2903. 2882-2904. 2884-2906. 2885-2907, 2886-2908, 2887-2909, 2888-2910, 2889-2911, 2180-2202, 440-462, 2045-2067, 2910-2932, 2914-2936, 2915-2937, 2916-2938, 2917-2939, 2918-2940, 2022-2044, 2023-2045, 103-125, 467-489, 1160-1182, 759-781, 1238-1260, 1869-1891, 1577-1599, 1871-1893, 940-962, 2614-2636, 2615-2637, 2933-2955, 2934-2956, 2884-2906, 2885-2907, 2886-2908, 519-541, 1029-1051, 726-748, 2312-2334, 2313-2335, 2943-2965, 3250-3272, 2316-2338, 2946-2968, 2947-2969, 2948-2970, 2950-2972, 2951-2973. 2952-2974. 2004- 2026, 3172-3194, 3344-3366, 3345-3367. 3325-3347. 3347-3369. 3348-3370. 3349-3371, 3316-3338, 2839-2861, 2958-2980, 2962-2984, 2963-2985, 2964-2986, 2965-2987, 2982-3004, 2858-2880, 2859-

[0049] 2881, 2088-2110, 1034-1056, 3135-3157, 3234-3256, 3091-3113, 3092-3114, 3004-3026, 3006-3028, 3007-3029, 3008-3030, 716-738, 492-514, 3153-3175, 854-876, 2343-2365, 3070-3092, 3071-3093, 3072-3094, 3073-3095, 3079-3101, 3080-3102, 1425-1447, 3082-3104, 3281-3303, 3257-3279. 417-439, 2129-2151, 3113-3135, 3114-3136, 407-429, 2879-2901, 2999-3021, 3000-3022, 3002-3024, 3003-3025, 3313-3335, 3314-3336, 3315-3337, 3232-3254, 3233-3255, 1176-1198, 1178-1200, 1416-1438, 10-32, 10-32, 12-34, 2149-2171, 13-35, 762-784, 2150-2172, 2151-2173, 1027-1049, 3601-3623, 1253-1275, 1254-1276, 3169-3191, 3172-3194, 3174-3196, 3175-3197, 3176-3198, 3177-3199, 3178-3200, 3179- 3201, 3180-3202, 3258-3280, 820-842, 822-844, 3214-3236, 43-65, 2031-2053. 2868-2890, 2176-2198, 1023-1045, 979-1001, 1108-1130. 3001-3023, 2762-2784, 641-663. 1200-1222. 2588-2610, 3501-3523, 3502-3524, 3309-3331, 3504-3526, 3316-3338, 3318-3340, 3319-3341. 3320-3342. 3321-3343. 3322- 3344, 3323-3345, 3570-3592, 3230-3252, 3361-3383, 3362-3384, 3363-3385, 3364-3386, 3365-3387, 3366-3388, 3324-3346, 1829-1851, 3399-3421, 3024-3046, 3648-3670, 3068-3090, 3426-3448, 2161- 2183, 3073-3095, 3429-3451, 3430-3452, 440-462, 441-463, 442-464, 3434-3456, 3198-3220, 3199- 3221, 3200-3222, 259-281, 260-282, 261-283, 262-284, 2194-2216, 1620-1642. 1621-1643, 1622-1644, 3042-3064, 3043-3065, 3044-3066, 2885-2907, 3046-3068, 3490-3512, 3491-3513. 2604-2626. 879-901, 2691-2713, 2692-2714, 3212-3234, 2695-2717, 2529-2551. 2151-2173. 2152-2174. 3613-3635. 3616- 3638, 1290-1312, 2170-2192, 3219-3241, 934-956, 3569-3591, 2219-2241, 3538-3560, 3539-3561, 3540- 3562, 3541-3563, 3542-3564, 3543-3565, 3545-3567, 2767-2789, 1377-1399, 3565-3587, 3327-3349, 1608-1630, 1126-1148, 803-825, 364-386, 366-388, 367-389, 619-641, 620-642, 3312-3334, 3187-3209, 2453-2475, 2046-2068, 1011-1033, 2054-2076, 1013-1035, 1014-1036, 1015-1037, 1016-1038. 1017- 1039, 3177-3199, 3178-3200, 48-70, 1503-1525, 3641-3663, 3651-3673, 1670-1692, 3514-3536, 3154- 3176, 3516-3538, 3199-3221. 3200-3222. 59-81, 2408-2430, 3491-3513, 3494-3516, 1627-1649, 3479- 3501, 3444-3466, 2992-3014, 2993-3015, 24-46, 3049-3071, 3050-3072, 3051-3073, 787-809, 790-812, 791-813, 2274-2296, 2275-2297, 2812-2834, 1613-1635, 2814-2836, 1615-1637, 1618-1640, 1619-1641, 1620-1642, 2659-2681, 1495-1517, 1496-1518, 3483-3505, 3484-3506, 3485-3507, 2297-2319, 2781- 2803, 2782-2804, 2783-2805, 2784-2806, 3497-3519, 2303-2325, 2968-2990, 2969-2991, 2970-2992, 3325-3347, 3326-3348, 3327-3349, 3328-3350, 3329-3351, 583-605, 584-606, 669-691, 922-944, 284- 306. 2836-2858. 2837-2859. 2223-2245, 2224-2246, 2225-2247, 2226-2248, 2227-2249, 2228-2250, 2229-2251, 2230-2252, 2231-2253, 2232-2254, 2233-2255, 3528-3550, 3568-3590, 1902-1924, 2451- 2473, 3224-3246, 1599-1621, 1600-1622, 3237-3259, 1530-1552, 3159-3181, 3030-3052, 3033-3055, 2185-2207, 152-174, 84-106, 1492-1514, 1493-1515, 3282-3304, 3200-3222, 3204-3226, 3206-3228, 1144-1166, 3207-3229, 3208-3230, 3643-3665, 815-837, 2282-2304, 2284-2306, 1829-1851, 1830-1852, 1915-1937, 148-170, 3610-3632, 3611-3633, 2574-2596, 2575-2597, 2576-2598, 2577-2599, 3198-3220, 3199-3221, 1315-1337, 345-367, 2870-2892, 2871-2893, 2223-2245, 2224-2246, 2476-2498. 2478-2500. 1481-1503, 1482-1504, 1927-1949, 1928-1950, 1929-1951, 1930-1952, 1931-1953, 3539-3561, 2332- 2354, 912-934, 3285-3307, 3268-3290, 1468-1490, 3270-3292, 549-571, 1166-1188, 3310-3332, 822- 844, 3312-3334, 3313-3335, 3314-3336, 3351-3373, 3524-3546, 3378-3400, 3354-3376, 3380-3402, 2087-2109, 2088-2110, 2811-2833, 1272-1294, 1540-1562, 3387-3409, 1308-1330, 99-121, 3659-3681, 989-1011, 1022-1044. 596-618, 1805-1827, 487-509, 488-510, 2603-2625, 2604-2626, 2605-2627, 1488- 1510, 3214-3236, 1653-1675, 3491-3513, 3456-3478, 3457-3479, 3459-3481, 3460-3482, 2961-2983, 3521-3543, 1029-1051, 2770-2792, 2771-2793, 2772-2794, 2328-2350, 751-773, 2400-2422, 2402-2424, 2403-2425, 2222-2244, 2816-2838, 2224-2246, 2235-2257, 2283-2305, 2884-2906, 2885-2907, 3293- 3315, 3294-3316, 3295-3317, 48-70, 52-74, 53-75, 2820-2842, 1610-1632, 1812-1834, 371-393, 712- 734, 1910-1932. 1911-1933, 3647-3669, 492-514. 711-733, 3651-3673, 3358-3380. 3327-3349. 3328- 3350, 3329-3351, 1628-1650, 170-192, 3137-3159, 3138-3160, 786-808, 20-42. 771-793. 745-767, 462- 484, 322-344, 3522-3544, 3523-3545, 3524-3546, 1670-1692, 1411-1433, 1505-1527, 1413-1435, 1507- 1529, 1044-1066, 3650-3672, 3207-3229, 1514-1536, 3226-3248, 3128-3150, 3340-3362, 3231-3253, 3232-3254, 2855-2877, 2856-2878, 2857-2879, 2456-2478, 2457-2479, 2658-2680, 1953-1975, 1954- 1976, 368-390, 1135-1157, 3560-3582, 1623-1645, 2858-2880, 848-870, 3284-3306, 52-74, 2559-2581, 2575-2597, 393-415, 1507-1529, 3154-3176, 3408-3430, 3494-3516, 3412-3434, 3111-3133, 3569-3591, 483-505, 2575-2597, 1402-1424, 3060-3082, 1630-1652, 172-194, 2102-2124, 1850-1872, 3014-3036, 3015-3037, 1866-1888, 1867-1889, 2808-2830, 2809-2831, 2810-2832, 2811-2833, 2812-2834, 2813- 2835, 2814-2836, 808-830, 269-291, 810-832, 2277-2299, 2278-2300, 2279-2301, 814-836, 2281-2303, 2282-2304, 721-743, 354-376, 355-377, 3063-3085, 2858-2880, 2860-2882, 1487-1509, 3225-3247, 2033-2055, 1488-1510, 1111-1133, 1554-1576, 2171-2193, 2047-2069, 3206-3228, 3283-3305. 3284- 3306, 3286-3308, 3287-3309, 3017-3039, 1494-1516, 1147-1169. 1148-1170. 1150-1172, 2968-2990, 3329-3351, 584-606, 795-817, 3603-3625, 2750-2772, 3299-3321, 3300-3322, 3222-3244, 3532-3554, 3533-3555, 1601-1623, 1467-1489, 2153-2175, 3661-3683, 3662-3684, 257-279, 1472-1494, 1473-1495, 3286-3308, 3287-3309, 741-763, 742-764, 826-848, 3550-3572, 3205-3227, 2521-2543, 3204-3226, 3470-3492, 3471-3493, 863-885, 864-886, 2756-2778, 3213-3235, 651-673, 3535-3557, 1166-1188, 1167-1189, 963-985, 77-99, 2257-2279, 437-459, 1144-1166, 313-335, 316-338, 2291-2313, 1838-1860, 1841-1863, 1260-1282, 340-362, 2090-2112, 2858-2880, 343-365, 3165-3187, 2880-2902, 851-873, 2606-2628, 1273-1295, 1546-1568, 933-955, 481-503, 401-423, 402-424. 403-425. 404-426, 407-429, 1398-1420, 3472-3494, 3490-3512, 3491-3513, 3492-3514, 3548-3570, 3549-3571, 3550-3572, 3551- 3573, 2301-2323, 2302-2324, 2303-2325, 2304-2326, 2305-2327, 3408-3430, 3290-3312, 1865-1887, 3525-3547, 3293-3315, 3527-3549, 3156-3178, 244-266, 246-268, 248-270, 3054-3076, 3055-3077, 2937-2959, 1850-1872, 1851-1873, 1852-1874, 1853-1875, 1854-1876, 1855-1877, 1856-1878. 2199- 2221, 2200-2222, 997-1019, 3157-3179, 3158-3180, 589-611. 1197-1219, 1198-1220, 1200-1222, 2608- 2630, 1202-1224, 2971-2993, 3347-3369. 2246-2268. 42-64, 1317-1339, 2499-2521, 3316-3338, 3317- 3339, 3110-3132, 1697-1719, 1698-1720, 3132-3154, 1154-1176, 1155-1177, 3556-3578, 3558-3580, 3560-3582, 1485-1507, 589-611, 2205-2227, 3540-3562, 2717-2739, 3280-3302, 3282-3304, 3555-3577, 3556-3578, 2851-2873, 2853-2875, 3087-3109, 3088-3110, 3089-3111, 1346-1368, 3347-3369, 1348- 1370, 597-619, 598-620, 599-621. 2188-2210, 3007-3029, 3008-3030, 3009-3031, 2722-2744, 2157- 2179, 2724-2746, 2725-2747, 2726-2748, 2727-2749. 1194-1216. 1195-1217. 1196-1218, 1197-1219, 1199-1221, 1200-1222, 2150-2172, or 2151-2173 of SEQ ID NO: 1. In some embodiments, the region of complementarity comprises at least 15 contiguous nucleotides from any one of nucleotides 381-403, 746- 768, 747-769, 263-285, 2465-2487, 248-270, 249-271, 251-273, 254-276, 255-277, 256-278, 258-280, 260-282, 263-285, 266-288, 272-294, 273-295, 274-296, 275-297, 276-298, 278-300, 279-301, 280-302, 281-303, 284-306. 285-307, 288-310, 289-311, 291-313, 309-331, 312-334. 313-335, 314-336, 315-337, 316-338, 317-339. 318-340. 319-341, 320-342, 321-343, 322-344, 323-345. 324-346, 325-347, 326-348, 327-349, 328-350, 329-351, 330-352, 333-355, 334-356, 336-358, 337-359, 339-361, 348-370, 349-371, 999-1021, 3004-3026, 3005-3027, 2903-2925, 2319-2341, 2905-2927, 360-382, 361-383, 362-384, 363- 385, 364-386, 365-387, 366-388, 367-389, 368-390, 369-391, 370-392, 371-393, 372-394, 373-395, 374-

[0050] 396, 375-397, 376-398, 377-399, 378-400, 381-403, 383-405, 384-406, 385-407, 386-408, 387-409, 388-

[0051] 410, 389-411, 397-419, 398-420, 399-421, 400-422. 401-423, 402-424, 403-425, 404-426, 405-427, 406-

[0052] 428. 407-429, 408-430, 409-431, 410-432, 411-433. 412-434. 413-435, 416-438, 417-439, 418-440, 419-

[0053] 441 420-442. 421-443. 422-444. 423-445. 3232-3254. 3233-3255. 426-448. 3235-3257. 3236-3258. 429-

[0054] 451, 430-452, 431-453, 432-454, 433-455, 434-456, 435.457, 436-458, 437-459, 438-460, 440-462, 444- 466, 445-467, 446-468, 448-470, 449-471, 451-473, 459-481, 467-489, 472-494, 473-495, 475-497, 476- 498, 477-499, 478-500, 479-501, 480-502, 481-503, 482-504, 483-505, 484-506, 485-507, 486-508, 487- 509. 488-510, 489-511, 490-512, 491-513, 492-514. 493-515, 494-516, 495-517, 496-518, 498-520, 423- 445. 500-522, 501-523, 502-524, 503-525, 504-526. 505-527. 506-528, 507-529, 508-530, 509-531, 510- 532, 511-533, 512-534, 513-535, 514-536, 515-537, 516-538, 517-539, 518-540, 520-542, 521-543, 522- 544, 523-545, 524-546, 525-547, 526-548, 527-549, 528-550, 530-552, 531-553, 534-556, 535-557, 580- 602, 581-603, 582-604, 583-605, 584-606, 585-607, 586-608, 587-609, 588-610, 589-611, 590-612, 591- 613, 592-614, 593-615, 594-616, 595-617, 596-618, 597-619, 598-620, 599-621, 600-622, 601-623, 603- 625. 605-627, 609-631, 610-632, 613-635, 614-636. 617-639, 618-640, 634-656, 636-658, 637-659, 639- 661. 640-662, 641-663, 642-664, 643-665, 646-668. 647-669. 650-672, 651-673, 654-676, 659-681, 660- 682, 662-684, 663-685, 669-691, 670-692, 671-693, 674-696, 675-697, 678-700, 715-737, 716-738, 717- 739, 720-742, 721-743, 722-744, 723-745, 724-746, 725-747, 726-748, 727-749, 728-750, 734-756, 737- 759, 740-762, 741-763, 745-767, 751-773, 754-776, 755-777, 756-778, 757-779, 761-783, 762-784, 763- 785, 764-786, 765-787, 766-788, 767-789, 769-791, 770-792, 776-798, 778-800, 780-802, 781-803, 783- 805. 785-807, 786-808, 788-810, 789-811, 790-812. 792-814, 808-830, 809-831, 811-833, 812-834, 813- 835. 815-837. 816-838, 817-839, 818-840, 825-847. 826-848. 828-850, 829-851, 831-853, 832-854, 833- 855, 855-877, 856-878, 857-879, 859-881, 860-882, 861-883, 862-884, 877-899, 878-900, 882-904, 884- 906, 887-909, 891-913, 895-917, 896-918, 898-920, 899-921, 901-923, 902-924, 904-926, 906-928, 907- 929, 908-930, 909-931, 910-932, 912-934, 913-935, 915-937, 916-938, 918-940, 920-942, 921-943, 922- 944, 923-945, 925-947, 926-948, 927-949, 928-950. 929-951, 931-953, 932-954, 933-955, 936-958, 937- 959. 939-961, 940-962, 941-963, 943-965, 944-966. 948-970, 951-973, 2868-2890, 319-341, 2933-2955, 2934-2956, 2935-2957, 2936-2958, 2937-2959, 2938-2960, 979-1001, 983-1005, 984-1006, 985-1007, 986-1008, 987-1009, 988-1010, 989-1011, 990-1012, 991-1013, 992-1014, 993-1015, 994-1016, 998- 1020, 999-1021, 1005-1027, 1012-1034, 1017-1039, 1018-1040, 1019-1041, 1020-1042, 1021-1043, 1022-1044, 1028-1050, 1029-1051, 1032-1054, 1039-1061, 1042-1064, 1044-1066, 1046-1068, 1083- 1105, 1084-1106, 1091-1113, 1144-1166, 1145-1167, 1147-1169. 1150-1172. 1154-1176, 1157-1179, 1160-1182, 1161-1183, 1162-1184, 1163-1185, 1165-1187, 1166-1188. 1167-1189. 1168-1190. 1169- 1191, 1170-1192, 1171-1193, 1172-1194, 1173-1195, 1174-1196, 1175-1197, 1176-1198, 1193-1215, 1194-1216, 1195-1217, 1196-1218, 1197-1219, 1198-1220, 1199-1221, 1200-1222, 1201-1223, 1202- 1224, 1203-1225, 1204-1226, 1205-1227, 1206-1228, 1227-1249, 1228-1250, 1229-1251, 1230-1252, 1233-1255, 1234-1256, 1235-1257, 1236-1258, 1237-1259, 1238-1260, 1239-1261, 1240-1262, 1241- 1263, 1242-1264, 1243-1265, 1244-1266, 1245-1267, 1248-1270. 1253-1275. 1255-1277, 1257-1279, 1260-1282, 1262-1284, 1263-1285, 1264-1286, 1265-1287. 1266-1288. 1268-1290. 1269-1291. 1270- 1292, 1273-1295, 1275-1297, 1277-1299, 1278-1300, 1301-1323, 1302-1324, 1303-1325, 1304-1326, 1305-1327, 1306-1328, 1307-1329, 1308-1330, 1309-1331, 1310-1332, 1311-1333, 1312-1334, 1313- 1335, 1314-1336, 1316-1338, 1334-1356, 1336-1358, 1338-1360, 1339-1361, 1340-1362, 2496-2518, 2497-2519, 2498-2520, 2499-2521, 1345-1367, 1346-1368, 1348-1370, 1349-1371, 1350-1372. 1351- 1373, 1352-1374, 1353-1375, 1356-1378, 1357-1379, 1358-1380. 1359-1381. 1360-1382, 1361-1383, 1362-1384, 1364-1386, 1365-1387, 1366-1388, 1367-1389. 1368-1390. 1369-1391. 1370-1392. 1371- 1393, 1372-1394, 1373-1395, 1374-1396, 1375-1397, 1376-1398, 1377-1399, 1378-1400, 1379-1401, 1380-1402, 1381-1403, 1382-1404, 3161-3183, 1390-1412, 1391-1413, 1392-1414, 1412-1434, 1413- 1435, 1414-1436, 1415-1437, 1416-1438, 1417-1439, 1418-1440, 1419-1441, 1420-1442, 1421-1443, 1422-1444, 1423-1445, 1424-1446, 1425-1447, 3572-3594, 3573-3595, 3082-3104, 1431-1453. 1447- 1469, 1449-1471, 1450-1472, 1451-1473, 1453-1475, 1454-1476. 1455-1477. 1456-1478, 1459-1481, 1460-1482, 2261-2283, 2476-2498, 1731-1753, 3576-3598. 1473-1495. 1474-1496. 1475-1497. 1476- 1498, 1477-1499, 1478-1500, 1495-1517, 1496-1518, 1497-1519, 1498-1520, 1499-1521, 1500-1522, 1501-1523, 1502-1524, 2144-2166, 1528-1550, 1532-1554, 1534-1556, 1537-1559, 1538-1560, 1550- 1572, 1556-1578, 1557-1579, 1558-1580, 1559-1581, 1562-1584, 1563-1585, 1569-1591, 1570-1592, 1572-1594, 1573-1595, 1576-1598, 1583-1605, 1584-1606, 1585-1607, 1586-1608, 1590-1612. 1591- 1613, 1594-1616, 1595-1617, 1596-1618, 1597-1619, 1598-1620. 1599-1621. 1600-1622, 1938-1960, 1157-1179, 1615-1637, 1616-1638, 1617-1639, 1618-1640. 1619-1641. 1620-1642. 1621-1643. 1622- 1644, 1623-1645, 1624-1646, 1625-1647, 1626-1648, 1627-1649, 1628-1650, 1629-1651, 1633-1655, 1634-1656, 1638-1660, 1639-1661, 1641-1663, 1642-1664, 1643-1665, 2965-2987, 3048-3070, 3049- 3071, 3050-3072, 1649-1671, 1650-1672, 1651-1673, 3241-3263, 3242-3264, 2773-2795, 2774-2796, 2858-2880, 1864-1886, 2652-2674, 2653-2675, 3634-3656, 1669-1691, 1670-1692, 1671-1693. 1672- 1694, 1673-1695, 1674-1696, 1675-1697, 1676-1698. 2651-2673. 2652-2674. 97-119, 3174-3196, 3175- 3197, 3176-3198, 3314-3336, 3290-3312, 3291-3313, 3292-3314, 1709-1731, 1710-1732, 490-512, 1543- 1565, 1544-1566, 414-436, 1509-1531, 1510-1532, 851-873, 2436-2458, 1720-1742, 1045-1067, 1046- 1068, 1747-1769, 1749-1771, 1752-1774, 1753-1775, 1754-1776, 1755-1777, 1758-1780, 1760-1782, 1761-1783, 1763-1785, 1765-1787, 1766-1788, 1768-1790, 1769-1791, 1771-1793, 1772-1794, 1773- 1795, 3130-3152, 3622-3644, 3623-3645, 1804-1826, 171-193, 172-194, 1814-1836, 1815-1837, 1681- 1703, 1817-1839, 1818-1840, 1820-1842, 1821-1843. 1823-1845. 1824-1846. 1826-1848, 1829-1851, 1833-1855, 1838-1860, 1840-1862, 1841-1863, 1844-1866, 1850-1872, 1852-1874, 443-465, 1854-1876, 1855-1877, 1856-1878, 1857-1879, 1858-1880, 1859-1881, 1860-1882, 1861-1883, 1862-1884, 1863- 1885, 1864-1886, 1865-1887, 1866-1888, 1867-1889, 1868-1890, 1869-1891, 1870-1892, 1871-1893, 1872-1894, 1873-1895, 1874-1896, 1875-1897, 1876-1898, 1877-1899, 1878-1900, 1884-1906, 1887- 1909, 1888-1910, 1891-1913, 1892-1914, 1893-1915, 1895-1917. 1898-1920. 1900-1922, 1901-1923, 1902-1924, 1907-1929, 1908-1930, 1909-1931, 1912-1934. 1930-1952. 1931-1953. 1932-1954. 1933- 1955, 1934-1956, 1935-1957, 1936-1958, 1937-1959, 1938-1960, 1939-1961, 1940-1962, 1941-1963, 1942-1964, 1943-1965, 1944-1966, 1945-1967, 1946-1968, 1947-1969, 1948-1970, 1949-1971, 1950- 1972, 1951-1973, 1952-1974, 1953-1975, 1954-1976, 1955-1977, 1956-1978, 1957-1979, 1958-1980, 1959-1981, 1960-1982, 1961-1983, 1962-1984, 1963-1985, 800-822, 2445-2467, 1985-2007, 1986-2008, 1987-2009, 1988-2010, 1989-2011, 1990-2012, 1991-2013, 1992-2014, 1993-2015. 1994-2016. 1995- 2017, 1996-2018, 1998-2020, 1999-2021. 2000-2022. 2035-2057. 3663-3685. 2037-2059, 2038-2060, 2039-2061, 2040-2062, 2041-2063, 2042-2064, 2043-2065, 2281-2303, 2282-2304, 2283-2305, 2053- 2075, 2054-2076, 2055-2077, 2056-2078, 2057-2079, 2058-2080, 2059-2081, 2062-2084, 2078-2100, 2079-2101, 2080-2102, 2081-2103, 2083-2105, 2084-2106, 2085-2107, 2087-2109, 2088-2110, 2090- 2112, 2093-2115, 2111-2133, 2124-2146, 2126-2148, 2127-2149, 2128-2150, 2130-2152, 2133-2155, 1887-1909, 3234-3256, 13-35, 1200-1222, 2184-2206, 2185-2207, 2186-2208, 2836-2858, 2837-2859, 2192-2214, 2194-2216, 2195-2217, 2196-2218, 2197-2219. 2198-2220. 2199-2221. 2200-2222. 2205- 2227, 2206-2228, 2208-2230, 2210-2232, 2211-2233, 2212-2234, 2215-2237, 2216-2238, 2870-2892, 2871-2893, 3455-3477, 2223-2245, 2225-2247, 2226-2248, 2227-2249, 2228-2250, 2230-2252, 2231- 2253, 2232-2254, 2233-2255, 2234-2256, 2235-2257, 2236-2258, 2240-2262, 2241-2263, 2242-2264, 2243-2265, 2244-2266, 2245-2267, 2246-2268, 2248-2270, 2249-2271, 2253-2275, 1062-1084. 1066- 1088, 2259-2281, 1309-1331, 3122-3144, 1764-1786, 17-39, 2288-2310, 2289-2311, 2290-2312, 2291- 2313, 2292-2314, 2293-2315, 2295-2317. 3521-3543. 2298-2320. 2300-2322. 2301-2323, 2304-2326, 2305-2327, 2306-2328, 2307-2329, 2308-2330, 2309-2331, 2310-2332, 2311-2333, 2312-2334, 2313- 2335, 2314-2336, 2315-2337, 2316-2338, 2317-2339, 2318-2340, 2322-2344, 3244-3266, 3245-3267, 3246-3268, 3324-3346, 3325-3347, 2336-2358, 2337-2359, 2338-2360, 2340-2362, 2341-2363, 2342- 2364, 2343-2365, 973-995, 2350-2372, 2351-2373, 3310-3332, 2977-2999, 2394-2416, 2396-2418, 2397- 2419, 2399-2421, 2400-2422, 2408-2430, 2409-2431. 2411-2433. 2412-2434. 2413-2435, 2414-2436, 1915-1937, 2418-2440, 1080-1102, 1295-1317, 1298-1320, 1121-1143, 1122-1144, 1123-1145, 1376- 1398, 1125-1147, 2448-2470, 2451-2473, 483-505, 484-506, 2575-2597, 2957-2979, 3027-3049, 3028- 3050, 1494-1516, 2660-2682, 261-283, 2481-2503, 2496-2518, 2507-2529, 2509-2531, 2556-2578, 2965- 2987, 3033-3055, 2582-2604, 2583-2605, 2585-2607, 2586-2608, 2595-2617, 2598-2620, 2599-2621, 2602-2624, 2603-2625, 2604-2626, 2605-2627, 2606-2628, 2607-2629, 2608-2630. 2609-2631. 2618- 2640, 2621-2643, 2625-2647, 2627-2649, 2629-2651. 2630-2652. 2631-2653. 2632-2654, 2633-2655, 2634-2656, 2636-2658, 2637-2659, 2638-2660, 2639-2661, 2641-2663, 2642-2664, 2647-2669, 2649- 2671, 2650-2672, 2652-2674, 2653-2675, 2656-2678, 2658-2680, 2659-2681, 2660-2682, 2661-2683, 2662-2684, 2663-2685, 2664-2686, 2665-2687, 2667-2689, 2672-2694, 2673-2695, 2674-2696, 2675- 2697, 2676-2698, 2681-2703, 2682-2704, 2706-2728, 1171-1193, 2708-2730, 2716-2738, 2717-2739, 2759-2781, 2761-2783, 2762-2784, 2763-2785, 2764-2786, 2765-2787, 2766-2788. 2767-2789. 2769- 2791, 2770-2792, 2772-2794, 2773-2795, 2776-2798. 2777-2799. 2778-2800. 2779-2801, 2810-2832, 2811-2833, 2812-2834, 2813-2835, 2815-2837, 2816-2838, 2817-2839, 2818-2840, 2819-2841, 2820- 2842, 2822-2844, 2823-2845, 2824-2846, 2825-2847, 2826-2848, 2827-2849, 2828-2850, 2829-2851, 2830-2852, 2831-2853, 2832-2854, 2833-2855, 2834-2856, 2835-2857, 2836-2858, 2837-2859, 2838- 2860, 2839-2861, 2840-2862, 2841-2863, 2842-2864, 2843-2865, 2847-2869, 2848-2870, 2849-2871, 2850-2872, 2851-2873, 2852-2874, 2853-2875, 2854-2876, 2855-2877, 1487-1509. 2227-2249. 2858-

[0055] 2880, 2859-2881, 3451-3473, 2861-2883. 2862-2884. 2863-2885. 2864-2886. 2865-2887, 2866-2888, 2869-2891, 2870-2892, 2871-2893, 2872-2894, 2873-2895, 2874-2896, 2875-2897, 2876-2898, 2877- 2899, 2878-2900, 2879-2901, 2880-2902, 2881-2903, 2882-2904, 2884-2906, 2885-2907, 2886-2908, 2887-2909, 2888-2910, 2889-2911, 2180-2202, 440-462, 2045-2067, 2910-2932, 2914-2936, 2915-2937, 2916-2938, 2917-2939, 2918-2940, 2022-2044, 2023-2045, 103-125, 467-489, 1160-1182, 759-781, 1238-1260, 1869-1891, 1577-1599, 1871-1893, 940-962, 2614-2636, 2615-2637, 2933-2955, 2934-2956, 2884-2906, 2885-2907, 2886-2908, 519-541, 1029-1051, 726-748, 2312-2334, 2313-2335, 2943-2965, 3250-3272, 2316-2338, 2946-2968, 2947-2969, 2948-2970, 2950-2972, 2951-2973, 2952-2974, 2004- 2026, 3172-3194, 3344-3366, 3345-3367, 3325-3347, 3347-3369, 3348-3370, 3349-3371, 3316-3338, 2839-2861, 2958-2980, 2962-2984, 2963-2985, 2964-2986, 2965-2987, 2982-3004, 2858-2880, 2859-

[0056] 2881, 2088-2110, 1034-1056, 3135-3157, 3234-3256, 3091-3113, 3092-3114. 3004-3026, 3006-3028, 3007-3029, 3008-3030, 716-738, 492-514, 3153-3175, 854-876, 2343-2365, 3070-3092, 3071-3093, 3072-3094, 3073-3095, 3079-3101, 3080-3102, 1425-1447. 3082-3104. 3281-3303. 3257-3279. 417-439. 2129-2151, 3113-3135, 3114-3136, 407-429, 2879-2901, 2999-3021, 3000-3022, 3002-3024, 3003-3025, 3313-3335, 3314-3336, 3315-3337, 3232-3254, 3233-3255, 1176-1198, 1178-1200, 1416-1438, 10-32, 10-32, 12-34, 2149-2171, 13-35, 762-784, 2150-2172, 2151-2173, 1027-1049, 3601-3623, 1253-1275, 1254-1276, 3169-3191, 3172-3194, 3174-3196, 3175-3197, 3176-3198, 3177-3199, 3178-3200. 3179- 3201, 3180-3202, 3258-3280, 820-842, 822-844, 3214-3236, 43-65. 2031-2053. 2868-2890, 2176-2198, 1023-1045, 979-1001, 1108-1130, 3001-3023, 2762-2784, 641-663, 1200-1222, 2588-2610, 3501-3523, 3502-3524, 3309-3331, 3504-3526, 3316-3338, 3318-3340, 3319-3341, 3320-3342, 3321-3343, 3322- 3344, 3323-3345, 3570-3592, 3230-3252, 3361-3383, 3362-3384, 3363-3385, 3364-3386, 3365-3387, 3366-3388, 3324-3346, 1829-1851, 3399-3421, 3024-3046, 3648-3670, 3068-3090, 3426-3448, 2161- 2183, 3073-3095, 3429-3451, 3430-3452, 440-462, 441-463, 442-464, 3434-3456, 3198-3220, 3199- 3221, 3200-3222, 259-281, 260-282, 261-283, 262-284. 2194-2216. 1620-1642. 1621-1643, 1622-1644, 3042-3064, 3043-3065, 3044-3066, 2885-2907, 3046-3068, 3490-3512, 3491-3513, 2604-2626, 879-901, 2691-2713, 2692-2714, 3212-3234, 2695-2717, 2529-2551, 2151-2173, 2152-2174, 3613-3635, 3616- 3638, 1290-1312, 2170-2192, 3219-3241, 934-956, 3569-3591, 2219-2241, 3538-3560, 3539-3561, 3540- 3562, 3541-3563, 3542-3564, 3543-3565, 3545-3567, 2767-2789, 1377-1399, 3565-3587, 3327-3349, 1608-1630, 1126-1148, 803-825, 364-386, 366-388. 367-389, 619-641, 620-642, 3312-3334, 3187-3209, 2453-2475, 2046-2068, 1011-1033, 2054-2076, 1013-1035. 1014-1036. 1015-1037. 1016-1038. 1017- 1039, 3177-3199, 3178-3200, 48-70, 1503-1525, 3641-3663, 3651-3673, 1670-1692, 3514-3536, 3154- 3176, 3516-3538, 3199-3221, 3200-3222, 59-81, 2408-2430, 3491-3513, 3494-3516, 1627-1649, 3479- 3501, 3444-3466, 2992-3014, 2993-3015, 24-46, 3049-3071, 3050-3072, 3051-3073, 787-809, 790-812, 791-813, 2274-2296, 2275-2297, 2812-2834, 1613-1635, 2814-2836, 1615-1637, 1618-1640, 1619-1641, 1620-1642, 2659-2681, 1495-1517, 1496-1518, 3483-3505, 3484-3506, 3485-3507. 2297-2319. 2781- 2803, 2782-2804, 2783-2805, 2784-2806. 3497-3519. 2303-2325. 2968-2990. 2969-2991, 2970-2992, 3325-3347, 3326-3348, 3327-3349, 3328-3350, 3329-3351, 583-605, 584-606, 669-691, 922-944, 284- 306, 2836-2858, 2837-2859, 2223-2245, 2224-2246, 2225-2247, 2226-2248, 2227-2249, 2228-2250, 2229-2251, 2230-2252, 2231-2253, 2232-2254, 2233-2255, 3528-3550, 3568-3590, 1902-1924, 2451- 2473, 3224-3246, 1599-1621, 1600-1622, 3237-3259, 1530-1552, 3159-3181, 3030-3052, 3033-3055, 2185-2207, 152-174, 84-106, 1492-1514, 1493-1515, 3282-3304, 3200-3222, 3204-3226, 3206-3228. 1144-1166, 3207-3229, 3208-3230, 3643-3665, 815-837, 2282-2304, 2284-2306, 1829-1851. 1830-1852. 1915-1937, 148-170, 3610-3632, 3611-3633, 2574-2596, 2575-2597, 2576-2598, 2577-2599, 3198-3220, 3199-3221, 1315-1337, 345-367, 2870-2892, 2871-2893, 2223-2245, 2224-2246, 2476-2498, 2478-2500, 1481-1503, 1482-1504, 1927-1949, 1928-1950, 1929-1951, 1930-1952, 1931-1953, 3539-3561, 2332- 2354, 912-934, 3285-3307, 3268-3290, 1468-1490, 3270-3292, 549-571, 1166-1188, 3310-3332, 822- 844. 3312-3334. 3313-3335, 3314-3336, 3351-3373, 3524-3546, 3378-3400, 3354-3376, 3380-3402, 2087-2109, 2088-2110, 2811-2833, 1272-1294, 1540-1562. 3387-3409. 1308-1330. 99-121, 3659-3681, 989-1011, 1022-1044, 596-618, 1805-1827, 487-509, 488-510, 2603-2625, 2604-2626, 2605-2627, 1488- 1510, 3214-3236, 1653-1675, 3491-3513, 3456-3478, 3457-3479, 3459-3481, 3460-3482, 2961-2983, 3521-3543, 1029-1051, 2770-2792, 2771-2793, 2772-2794, 2328-2350, 751-773, 2400-2422, 2402-2424, 2403-2425, 2222-2244, 2816-2838, 2224-2246, 2235-2257, 2283-2305, 2884-2906, 2885-2907. 3293- 3315, 3294-3316, 3295-3317, 48-70, 52-74, 53-75, 2820-2842, 1610-1632, 1812-1834, 371-393, 712- 734, 1910-1932, 1911-1933, 3647-3669, 492-514, 711-733, 3651-3673, 3358-3380, 3327-3349, 3328- 3350, 3329-3351, 1628-1650, 170-192, 3137-3159, 3138-3160, 786-808, 20-42, 771-793, 745-767, 462- 484, 322-344, 3522-3544, 3523-3545, 3524-3546, 1670-1692, 1411-1433, 1505-1527, 1413-1435, 1507- 1529, 1044-1066, 3650-3672, 3207-3229, 1514-1536, 3226-3248, 3128-3150, 3340-3362, 3231-3253, 3232-3254, 2855-2877, 2856-2878, 2857-2879, 2456-2478, 2457-2479, 2658-2680. 1953-1975. 1954- 1976, 368-390, 1135-1157, 3560-3582, 1623-1645, 2858-2880, 848-870, 3284-3306, 52-74, 2559-2581, 2575-2597, 393-415, 1507-1529, 3154-3176, 3408-3430, 3494-3516, 3412-3434, 3111-3133, 3569-3591, 483-505, 2575-2597, 1402-1424, 3060-3082, 1630-1652, 172-194, 2102-2124, 1850-1872, 3014-3036, 3015-3037, 1866-1888, 1867-1889, 2808-2830, 2809-2831, 2810-2832, 2811-2833, 2812-2834, 2813- 2835, 2814-2836, 808-830, 269-291, 810-832, 2277-2299, 2278-2300, 2279-2301, 814-836, 2281-2303, 2282-2304, 721-743, 354-376, 355-377. 3063-3085. 2858-2880, 2860-2882, 1487-1509, 3225-3247, 2033-2055, 1488-1510, 1111-1133, 1554-1576, 2171-2193. 2047-2069. 3206-3228. 3283-3305. 3284- 3306, 3286-3308, 3287-3309, 3017-3039, 1494-1516, 1147-1169, 1148-1170, 1150-1172, 2968-2990, 3329-3351, 584-606, 795-817, 3603-3625, 2750-2772, 3299-3321, 3300-3322, 3222-3244, 3532-3554, 3533-3555, 1601-1623, 1467-1489, 2153-2175, 3661-3683, 3662-3684, 257-279, 1472-1494, 1473-1495, 3286-3308, 3287-3309, 741-763, 742-764, 826-848, 3550-3572, 3205-3227, 2521-2543, 3204-3226, 3470-3492, 3471-3493, 863-885, 864-886, 2756-2778, 3213-3235, 651-673, 3535-3557, 1166-1188, 1167-1189, 963-985, 77-99. 2257-2279. 437-459. 1144-1166. 313-335, 316-338, 2291-2313, 1838-1860, 1841-1863, 1260-1282, 340-362, 2090-2112, 2858-2880, 343-365, 3165-3187, 2880-2902, 851-873, 2606-2628, 1273-1295, 1546-1568, 933-955, 481-503, 401-423, 402-424, 403-425, 404-426, 407-429, 1398-1420, 3472-3494, 3490-3512, 3491-3513, 3492-3514, 3548-3570, 3549-3571, 3550-3572, 3551- 3573, 2301-2323, 2302-2324, 2303-2325, 2304-2326, 2305-2327, 3408-3430, 3290-3312, 1865-1887, 3525-3547, 3293-3315, 3527-3549, 3156-3178, 244-266, 246-268, 248-270, 3054-3076, 3055-3077, 2937-2959, 1850-1872, 1851-1873, 1852-1874, 1853-1875. 1854-1876. 1855-1877. 1856-1878. 2199- 2221, 2200-2222, 997-1019, 3157-3179, 3158-3180, 589-611, 1197-1219, 1198-1220, 1200-1222, 2608- 2630, 1202-1224, 2971-2993, 3347-3369, 2246-2268, 42-64, 1317-1339, 2499-2521, 3316-3338, 3317- 3339, 3110-3132, 1697-1719, 1698-1720, 3132-3154, 1154-1176, 1155-1177, 3556-3578, 3558-3580, 3560-3582, 1485-1507, 589-611, 2205-2227, 3540-3562, 2717-2739, 3280-3302, 3282-3304, 3555-3577, 3556-3578, 2851-2873, 2853-2875, 3087-3109, 3088-3110, 3089-3111, 1346-1368. 3347-3369. 1348- 1370, 597-619, 598-620, 599-621. 2188-2210, 3007-3029, 3008-3030, 3009-3031, 2722-2744, 2157- 2179, 2724-2746, 2725-2747, 2726-2748, 2727-2749, 1194-1216, 1195-1217, 1196-1218, 1197-1219, 1199-1221, 1200-1222, 2150-2172, or 2151-2173 of SEQ ID NO: 1.

[0057] In one embodiment, the antisense strand comprises at least 15 contiguous nucleotides differing by nor more than 0. 1, 2, or 3 nucleotides from any one of tire antisense strand nucleotide sequences of a duplex selected from the group consisting of AD-2320680, AD-2320683, AD-2320684. AD-2320739, AD-2320769, AD-2320870, AD-2320871, AD-2320873, AD-2320876, AD-2320877, AD-2320878, AD

[0058] 2320880, AD-2320882, AD-2320885, AD-2320938, AD-2320944, AD-2320945, AD-2320946, AD-

[0059] 2320947, AD-2320948, AD-2320950, AD-2320951, AD-2320952, AD-2320953, AD-2320956, AD-

[0060] 2320957, AD-2320960, AD-2320961, AD-2320963, AD-2320981, AD-2320984, AD-2320985, AD-

[0061] 2320986, AD-2321037, AD-2321038. AD-2321039, AD-2321040, AD-2321041, AD-2321042. AD-

[0062] 2321043, AD-2321044, AD-2321045. AD-2321046, AD-2321047, AD-2321048, AD-2321049. AD-

[0063] 2321050, AD-2321051, AD-2321052, AD-2321055, AD-2321056, AD-2321058, AD-2321059, AD-

[0064] 2321061, AD-2321070, AD-2321071, AD-2321073, AD-2321076, AD-2321077, AD-2321079, AD-

[0065] 2321080, AD-2321081, AD-2321082, AD-2321083, AD-2321084, AD-2321085, AD-2321086, AD-

[0066] 2321137, AD-2321138, AD-2321139, AD-2321140, AD-2321141, AD-2321142, AD-2321143, AD-

[0067] 2321144, AD-2321145, AD-2321146. AD-2321147, AD-2321148, AD-2321149, AD-2321150. AD-

[0068] 2321153, AD-2321155, AD-2321156. AD-2321157, AD-2321158, AD-2321159, AD-2321160. AD-

[0069] 2321161, AD-2321169, AD-2321170, AD-2321171, AD-2321172, AD-2321173, AD-2321174, AD-

[0070] 2321175, AD-2321176, AD-2321177, AD-2321178, AD-2321179, AD-2321180, AD-2321181, AD-

[0071] 2321182, AD-2321183, AD-2321184, AD-2321185, AD-2321238, AD-2321239, AD-2321240, AD-

[0072] 2321241, AD-2321242, AD-2321243, AD-2321244, AD-2321245, AD-2321246, AD-2321247, AD-

[0073] 2321248, AD-2321249, AD-2321250. AD-2321251, AD-2321252, AD-2321253, AD-2321254. AD-

[0074] 2321255, AD-2321256, AD-2321257. AD-2321258, AD-2321259, AD-2321260. AD-2321262. AD-

[0075] 2321266, AD-2321267, AD-2321268, AD-2321270, AD-2321271, AD-2321273, AD-2321281, AD-

[0076] 2321339, AD-2321344, AD-2321345, AD-2321347, AD-2321348, AD-2321349, AD-2321350, AD-

[0077] 2321351, AD-2321352, AD-2321353, AD-2321354, AD-2321355, AD-2321356, AD-2321357, AD-

[0078] 2321358, AD-2321359, AD-2321360, AD-2321361, AD-2321362, AD-2321363, AD-2321364, AD-

[0079] 2321365, AD-2321366, AD-2321367. AD-2321368, AD-2321370, AD-2321371, AD-2321372. AD-

[0080] 2321373, AD-2321374, AD-2321375. AD-2321376, AD-2321377, AD-2321378. AD-2321379. AD-

[0081] 2321380, AD-2321381, AD-2321382, AD-2321383, AD-2321384, AD-2321385, AD-2321386, AD-

[0082] 2321437, AD-2321438, AD-2321439, AD-2321440, AD-2321442, AD-2321443, AD-2321444, AD-

[0083] 2321445, AD-2321446, AD-2321447, AD-2321448, AD-2321449, AD-2321450, AD-2321452, AD-

[0084] 2321453, AD-2321456, AD-2321457, AD-2321552, AD-2321553, AD-2321554, AD-2321555. AD-

[0085] 2321556, AD-2321557, AD-2321558. AD-2321559, AD-2321560, AD-2321561, AD-2321562. AD-

[0086] 2321563, AD-2321564, AD-2321565. AD-2321566, AD-2321567, AD-2321568. AD-2321569. AD-

[0087] 2321570, AD-2321571, AD-2321572, AD-2321573, AD-2321575, AD-2321577, AD-2321581, AD-

[0088] 2321582, AD-2321585, AD-2321586, AD-2321639, AD-2321640, AD-2321656, AD-2321658, AD-

[0089] 2321659, AD-2321661, AD-2321662, AD-2321663, AD-2321664, AD-2321665, AD-2321668, AD-

[0090] 2321669, AD-2321672, AD-2321673, AD-2321676, AD-2321681, AD-2321682, AD-2321684. AD-

[0091] 2321685, AD-2321741, AD-2321742. AD-2321743, AD-2321746, AD-2321747, AD-2321750. AD- 2321837, AD-2321838, AD-2321839, AD-2321842, AD-2321843, AD-2321844, AD-2321845, AD- 2321846, AD-2321847, AD-2321848, AD-2321849, AD-2321850, AD-2321856, AD-2321859, AD- 2321862, AD-2321863, AD-2321867, AD-2321873, AD-2321876, AD-2321877, AD-2321878, AD- 2321879, AD-2321883, AD-2321884, AD-2321885, AD-2321886, AD-2321937, AD-2321938, AD- 2321939, AD-2321941, AD-2321942. AD-2321948, AD-2321950, AD-2321952, AD-2321953. AD- 2321955, AD-2321957, AD-2321958. AD-2321960, AD-2321961, AD-2321962, AD-2321964. AD- 2321980, AD-2321981, AD-2321983, AD-2321984, AD-2321985, AD-2322037, AD-2322038, AD- 2322039, AD-2322040, AD-2322047, AD-2322048, AD-2322050, AD-2322051, AD-2322053, AD- 2322054, AD-2322055, AD-2322057, AD-2322058, AD-2322059, AD-2322061, AD-2322062, AD- 2322063, AD-2322064, AD-2322079, AD-2322080, AD-2322084, AD-2322086, AD-2322139, AD- 2322143, AD-2322147, AD-2322148. AD-2322150, AD-2322151, AD-2322153, AD-2322154. AD- 2322156, AD-2322158, AD-2322159. AD-2322160, AD-2322161, AD-2322162, AD-2322164. AD- 2322165, AD-2322167, AD-2322168, AD-2322170, AD-2322172, AD-2322173, AD-2322174, AD- 2322175, AD-2322177, AD-2322178, AD-2322179, AD-2322180, AD-2322181, AD-2322183, AD- 2322184, AD-2322185, AD-2322238, AD-2322239, AD-2322241, AD-2322242, AD-2322243, AD- 2322245, AD-2322246, AD-2322250, AD-2322253, AD-2322254, AD-2322257, AD-2322260, AD- 2322261, AD-2322262, AD-2322263. AD-2322264, AD-2322265, AD-2322281, AD-2322285. AD- 2322286, AD-2322337, AD-2322338. AD-2322339, AD-2322340, AD-2322341. AD-2322342. AD- 2322343, AD-2322344, AD-2322345, AD-2322346, AD-2322350, AD-2322351, AD-2322357, AD- 2322364, AD-2322369, AD-2322370, AD-2322371, AD-2322372, AD-2322373, AD-2322374, AD- 2322380, AD-2322381, AD-2322384, AD-2322441, AD-2322444, AD-2322446, AD-2322448, AD- 2322485, AD-2322486, AD-2322543, AD-2322646, AD-2322647, AD-2322649, AD-2322652, AD- 2322656, AD-2322659, AD-2322662. AD-2322663, AD-2322664, AD-2322665, AD-2322667. AD- 2322668, AD-2322669, AD-2322670. AD-2322671, AD-2322672, AD-2322673. AD-2322674. AD- 2322675, AD-2322676, AD-2322677, AD-2322678, AD-2322745, AD-2322746, AD-2322747, AD- 2322748, AD-2322749, AD-2322750, AD-2322751, AD-2322752, AD-2322753, AD-2322754, AD- 2322755, AD-2322756, AD-2322757, AD-2322758, AD-2322779, AD-2322780, AD-2322781, AD- 2322782, AD-2322785, AD-2322786, AD-2322837, AD-2322838, AD-2322839, AD-2322840. AD- 2322841, AD-2322842, AD-2322843. AD-2322844, AD-2322845, AD-2322846, AD-2322847. AD- 2322850, AD-2322855, AD-2322857. AD-2322859, AD-2322862, AD-2322864. AD-2322865. AD- 2322866, AD-2322867, AD-2322868, AD-2322870, AD-2322871, AD-2322872, AD-2322875, AD- 2322877, AD-2322879, AD-2322880, AD-2322883, AD-2322884, AD-2322885, AD-2322886, AD- 2322937, AD-2322938, AD-2322939, AD-2322940, AD-2322941, AD-2322942, AD-2322943, AD- 2322944, AD-2322945, AD-2322946, AD-2322948, AD-2322966, AD-2322968, AD-2322970. AD- 2322971, AD-2322972, AD-2322973. AD-2322974, AD-2322975, AD-2322976, AD-2322977. AD- 2322978, AD-2322980, AD-2322981, AD-2322982, AD-2322983, AD-2322984, AD-2322985, AD- 2323038, AD-2323039, AD-2323040, AD-2323041, AD-2323042, AD-2323043, AD-2323044, AD- 2323046, AD-2323047, AD-2323048, AD-2323049, AD-2323050, AD-2323051, AD-2323052, AD- 2323053, AD-2323054, AD-2323055, AD-2323056, AD-2323057, AD-2323058, AD-2323059, AD- 2323060, AD-2323061, AD-2323062. AD-2323063, AD-2323064, AD-2323070, AD-2323072. AD- 2323073, AD-2323074, AD-2323144. AD-2323145, AD-2323146, AD-2323147, AD-2323148. AD- 2323149, AD-2323150, AD-2323151, AD-2323152, AD-2323153, AD-2323154, AD-2323155, AD- 2323156, AD-2323157, AD-2323158, AD-2323159, AD-2323160, AD-2323163, AD-2323179, AD- 2323181, AD-2323182, AD-2323183, AD-2323185, AD-2323186, AD-2323237, AD-2323238, AD- 2323241, AD-2323242, AD-2323248, AD-2323249, AD-2323253, AD-2323254, AD-2323255, AD- 2323256, AD-2323257, AD-2323258. AD-2323259, AD-2323260, AD-2323277, AD-2323278. AD- 2323279, AD-2323280, AD-2323281. AD-2323282, AD-2323283, AD-2323284, AD-2323357. AD- 2323360, AD-2323364, AD-2323366, AD-2323369, AD-2323370, AD-2323382, AD-2323438, AD- 2323439, AD-2323440, AD-2323441, AD-2323444, AD-2323445, AD-2323451, AD-2323452, AD- 2323454, AD-2323455, AD-2323458, AD-2323465, AD-2323466, AD-2323467, AD-2323468, AD- 2323472, AD-2323473, AD-2323476, AD-2323477, AD-2323478, AD-2323479, AD-2323480, AD- 2323481, AD-2323482, AD-2323544. AD-2323546, AD-2323547, AD-2323548, AD-2323549. AD- 2323550, AD-2323551, AD-2323552. AD-2323553, AD-2323554, AD-2323555. AD-2323556. AD- 2323557, AD-2323558, AD-2323559, AD-2323560, AD-2323561, AD-2323565, AD-2323566, AD- 2323570, AD-2323571, AD-2323573, AD-2323574, AD-2323575, AD-2323577, AD-2323578, AD- 2323579, AD-2323580, AD-2323581, AD-2323582, AD-2323583, AD-2323584, AD-2323585, AD- 2323586, AD-2323637, AD-2323638, AD-2323639, AD-2323641, AD-2323642, AD-2323648, AD- 2323651, AD-2323652, AD-2323653. AD-2323654, AD-2323655, AD-2323656, AD-2323657. AD- 2323658, AD-2323681, AD-2323682. AD-2323683, AD-2323684, AD-2323685. AD-2323686. AD- 2323737, AD-2323738, AD-2323739, AD-2323740, AD-2323741, AD-2323742, AD-2323743, AD- 2323744, AD-2323745, AD-2323746, AD-2323747, AD-2323748, AD-2323749, AD-2323751, AD- 2323752, AD-2323771, AD-2323772, AD-2323779, AD-2323781, AD-2323784, AD-2323785, AD- 2323786, AD-2323837, AD-2323840, AD-2323842, AD-2323843, AD-2323845, AD-2323847. AD- 2323848, AD-2323850, AD-2323851. AD-2323853, AD-2323854, AD-2323855, AD-2323856. AD- 2323858, AD-2323859, AD-2323886. AD-2323940, AD-2323941, AD-2323946. AD-2323947. AD- 2323948, AD-2323949, AD-2323950, AD-2323952, AD-2323953, AD-2323955, AD-2323956, AD- 2323958, AD-2323961, AD-2323965, AD-2323970, AD-2323972, AD-2323973, AD-2323976, AD- 2323982, AD-2323984, AD-2323985, AD-2323986, AD-2324037, AD-2324038, AD-2324039, AD- 2324040, AD-2324041, AD-2324042, AD-2324043, AD-2324044, AD-2324045, AD-2324046. AD- 2324047, AD-2324048, AD-2324049. AD-2324050, AD-2324051, AD-2324052, AD-2324053. AD- 2324054, AD-2324055, AD-2324056, AD-2324057, AD-2324058, AD-2324059, AD-2324060, AD- 2324066, AD-2324069, AD-2324070, AD-2324073, AD-2324074, AD-2324075, AD-2324077, AD- 2324080, AD-2324082, AD-2324083, AD-2324084, AD-2324139, AD-2324140, AD-2324141, AD- 2324144, AD-2324162, AD-2324163, AD-2324164, AD-2324165, AD-2324166, AD-2324167, AD- 2324168, AD-2324169, AD-2324170. AD-2324171, AD-2324172, AD-2324173, AD-2324174. AD- 2324175, AD-2324176, AD-2324177. AD-2324178, AD-2324179, AD-2324180, AD-2324181. AD- 2324182, AD-2324183, AD-2324184, AD-2324185, AD-2324186, AD-2324237, AD-2324238, AD- 2324239, AD-2324240, AD-2324241, AD-2324242, AD-2324243, AD-2324244, AD-2324245, AD- 2324246, AD-2324247, AD-2324267, AD-2324268, AD-2324269, AD-2324270, AD-2324271, AD- 2324272, AD-2324273, AD-2324274, AD-2324275, AD-2324276, AD-2324277, AD-2324278, AD- 2324280, AD-2324281, AD-2324282. AD-2324347, AD-2324348, AD-2324349, AD-2324350. AD- 2324351, AD-2324352, AD-2324353. AD-2324354, AD-2324355, AD-2324356, AD-2324357. AD- 2324358, AD-2324365, AD-2324366, AD-2324367, AD-2324368, AD-2324369, AD-2324370, AD- 2324371, AD-2324374, AD-2324440, AD-2324441, AD-2324442, AD-2324443, AD-2324445, AD- 2324446, AD-2324447, AD-2324449, AD-2324450, AD-2324452, AD-2324455, AD-2324473, AD- 2324486, AD-2324538, AD-2324539, AD-2324540, AD-2324542, AD-2324545, AD-2324572, AD- 2324586, AD-2324639, AD-2324640. AD-2324646, AD-2324647, AD-2324648, AD-2324649. AD- 2324650, AD-2324654, AD-2324656. AD-2324657, AD-2324658, AD-2324659. AD-2324660. AD- 2324661, AD-2324662, AD-2324667, AD-2324668, AD-2324670, AD-2324672, AD-2324673, AD- 2324674, AD-2324677, AD-2324678, AD-2324681, AD-2324682, AD-2324684, AD-2324685, AD- 2324737, AD-2324738, AD-2324739, AD-2324740, AD-2324742, AD-2324743, AD-2324744, AD- 2324745, AD-2324746, AD-2324747, AD-2324748, AD-2324752, AD-2324753, AD-2324754, AD- 2324755, AD-2324756, AD-2324757. AD-2324758, AD-2324760, AD-2324761, AD-2324765. AD- 2324766, AD-2324770, AD-2324771. AD-2324772, AD-2324775, AD-2324777. AD-2324778. AD- 2324779, AD-2324780, AD-2324781, AD-2324782, AD-2324783, AD-2324784, AD-2324786, AD- 2324837, AD-2324839, AD-2324841, AD-2324842, AD-2324845, AD-2324846, AD-2324847, AD- 2324848, AD-2324849, AD-2324850, AD-2324851, AD-2324852, AD-2324853, AD-2324854, AD- 2324855, AD-2324856, AD-2324857, AD-2324858, AD-2324859, AD-2324863, AD-2324864. AD- 2324865, AD-2324866, AD-2324867. AD-2324868, AD-2324877, AD-2324878, AD-2324879. AD- 2324881, AD-2324882, AD-2324883. AD-2324884, AD-2324886, AD-2324941. AD-2324942. AD- 2324946, AD-2324947, AD-2324985, AD-2325037, AD-2325038, AD-2325040, AD-2325041, AD- 2325049, AD-2325050, AD-2325052, AD-2325053, AD-2325054, AD-2325055, AD-2325058, AD- 2325059, AD-2325066, AD-2325077, AD-2325080, AD-2325081, AD-2325082, AD-2325083, AD- 2325084, AD-2325085, AD-2325139, AD-2325142, AD-2325145, AD-2325146, AD-2325147. AD- 2325148, AD-2325149, AD-2325150. AD-2325151, AD-2325152, AD-2325154, AD-2325172. AD- 2325237, AD-2325248, AD-2325250, AD-2325277, AD-2325349, AD-2325350, AD-2325353, AD- 2325354, AD-2325356, AD-2325357, AD-2325366, AD-2325369, AD-2325370, AD-2325373, AD- 2325374, AD-2325375, AD-2325376, AD-2325377, AD-2325378, AD-2325379, AD-2325380, AD- 2325439, AD-2325442, AD-2325446, AD-2325448, AD-2325450, AD-2325451, AD-2325452, AD- 2325453, AD-2325454, AD-2325455. AD-2325457, AD-2325458, AD-2325459, AD-2325460. AD- 2325462, AD-2325463, AD-2325468. AD-2325470, AD-2325471, AD-2325473, AD-2325474. AD- 2325477, AD-2325479, AD-2325480, AD-2325481, AD-2325482, AD-2325483, AD-2325484, AD- 2325485, AD-2325486, AD-2325538, AD-2325543, AD-2325544, AD-2325545, AD-2325546, AD- 2325547, AD-2325552, AD-2325553, AD-2325557, AD-2325558, AD-2325559, AD-2325567, AD- 2325568, AD-2325640, AD-2325642, AD-2325643, AD-2325644, AD-2325645, AD-2325646, AD- 2325647, AD-2325648, AD-2325650. AD-2325651, AD-2325653, AD-2325654, AD-2325657. AD- 2325658, AD-2325659, AD-2325660. AD-2325671, AD-2325672, AD-2325673, AD-2325674. AD- 2325676, AD-2325677, AD-2325678, AD-2325679, AD-2325680, AD-2325681, AD-2325683, AD- 2325684, AD-2325685, AD-2325686, AD-2325737, AD-2325738, AD-2325739, AD-2325740, AD- 2325741, AD-2325742, AD-2325743, AD-2325744, AD-2325745, AD-2325746, AD-2325747, AD- 2325748, AD-2325749, AD-2325750, AD-2325751, AD-2325752, AD-2325753, AD-2325754, AD- 2325758, AD-2325759, AD-2325760. AD-2325761, AD-2325762, AD-2325763, AD-2325764. AD- 2325765, AD-2325766, AD-2325767. AD-2325768, AD-2325769, AD-2325770. AD-2325771. AD- 2325772, AD-2325773, AD-2325774, AD-2325775, AD-2325776, AD-2325777, AD-2325780, AD- 2325781, AD-2325782, AD-2325783, AD-2325784, AD-2325785, AD-2325786, AD-2325837, AD- 2325838, AD-2325839, AD-2325840, AD-2325841, AD-2325842, AD-2325843, AD-2325845, AD- 2325846, AD-2325847, AD-2325848, AD-2325849, AD-2325850, AD-2325874, AD-2325881, AD- 2325882, AD-2325883, AD-2325937. AD-2325938, AD-2325939, AD-2325940, AD-2325941. AD- 2325942, AD-2325943, AD-2325944. AD-2325945, AD-2325946, AD-2325947. AD-2325948. AD- 2325949, AD-2325950, AD-2325951, AD-2325952, AD-2325953, AD-2325954, AD-2325955, AD- 2325956, AD-2325957, AD-2325958, AD-2325959, AD-2325960, AD-2325961, AD-2325962, AD- 2325963, AD-2325964, AD-2325965, AD-2325966, AD-2325967, AD-2325968, AD-2325969, AD- 2325970, AD-2325972, AD-2325973, AD-2325974, AD-2325975, AD-2325976, AD-2325977. AD- 2325978, AD-2325979, AD-2325980. AD-2325981, AD-2325982, AD-2325983, AD-2325984. AD- 2325985, AD-2326039, AD-2326040. AD-2326041, AD-2326042, AD-2326059. AD-2326060. AD- 2326061, AD-2326067, AD-2326069, AD-2326070, AD-2326072, AD-2326073, AD-2326074, AD- 2326075, AD-2326077, AD-2326078, AD-2326079, AD-2326080, AD-2326170, AD-2326242, AD- 2326243, AD-2326244, AD-2326245, AD-2326246, AD-2326247, AD-2326248, AD-2326254, AD- 2326255, AD-2326256, AD-2326257, AD-2326273, AD-2326274, AD-2326275, AD-2326286. AD- 2326340, AD-2326341, AD-2326342. AD-2326348, AD-2326349, AD-2326350, AD-2326352. AD- 2326353, AD-2326354, AD-2326355, AD-2326356, AD-2326769, AD-2326770, AD-2326781, AD- 2326783, AD-2326785, AD-2326846, AD-2326847, AD-2326848, AD-2326849, AD-2326850, AD- 2326851, AD-2326852, AD-2326853, AD-2326858, AD-2326876, AD-2326881, AD-2326882, AD- 2326885, AD-2326938, AD-2326940, AD-2326941, AD-2326942, AD-2326943, AD-2326944, AD- 2326945, AD-2326946, AD-2327065. AD-2327067, AD-2327069, AD-2327070, AD-2327071. AD- 2327072, AD-2327073, AD-2327076. AD-2327077, AD-2327079, AD-2327080, AD-2327154. AD- 2327157, AD-2327158, AD-2327159, AD-2327160, AD-2327161, AD-2327162, AD-2327163, AD- 2327164, AD-2327172, AD-2327174, AD-2327175, AD-2327176, AD-2327177, AD-2327178, AD- 2327179, AD-2327262, AD-2327263, AD-2327264, AD-2327265, AD-2327266, AD-2327267, AD- 2327268, AD-2327269, AD-2327345, AD-2327371, AD-2327372, AD-2327374, AD-2327379, AD- 2327461, AD-2327464, AD-2327465. AD-2327466, AD-2327467, AD-2327468, AD-2327469. AD- 2327470, AD-2327471, AD-2327472. AD-2327473, AD-2327474, AD-2327475, AD-2327551. AD- 2327552, AD-2327553, AD-2327554, AD-2327555, AD-2327556, AD-2327557, AD-2327558, AD- 2327559, AD-2327560, AD-2327561, AD-2327562, AD-2327563, AD-2327564, AD-2327565, AD- 2327566, AD-2327567, AD-2327568, AD-2327569, AD-2327571, AD-2327572, AD-2327573, AD- 2327574, AD-2327575, AD-2327576, AD-2327579, AD-2327580, AD-2327658, AD-2327659, AD- 2327660, AD-2327662, AD-2327665. AD-2327670, AD-2327671, AD-2327672, AD-2327673. AD- 2327674, AD-2327675, AD-2327677. AD-2327679, AD-2327684, AD-2327738. AD-2327742. AD- 2327747, AD-2327753, AD-2327755, AD-2327756, AD-2327758, AD-2327759, AD-2327761, AD- 2327762, AD-2327771, AD-2327774, AD-2327775, AD-2327776, AD-2327777, AD-2327778, AD- 2327779, AD-2327780, AD-2327781, AD-2327782, AD-2327783, AD-2327784, AD-2327785, AD- 2327846, AD-2327849, AD-2327856, AD-2327866, AD-2327867, AD-2327868, AD-2327869, AD- 2327870, AD-2327871, AD-2327872. AD-2327940, AD-2327943, AD-2327944, AD-2327947. AD- 2327960, AD-2327961, AD-2327962. AD-2328051, AD-2328052, AD-2328053. AD-2328054. AD- 2328055, AD-2328056, AD-2328057, AD-2328060, AD-2328061, AD-2328065, AD-2328066, AD- 2328067, AD-2328068, AD-2328069, AD-2328070, AD-2328071, AD-2328072, AD-2328073, AD- 2328074, AD-2328075, AD-2328076, AD-2328077, AD-2328078, AD-2328079, AD-2328080, AD- 2328081, AD-2328082, AD-2328083, AD-2328084, AD-2328085, AD-2328086, AD-2328137. AD- 2328138, AD-2328139, AD-2328140. AD-2328141, AD-2328142, AD-2328143, AD-2328144. AD- 2328145, AD-2328146, AD-2328171. AD-2328172, AD-2328179, AD-2328182. AD-2328183. AD- 2328184, AD-2328185, AD-2328186, AD-2328237, AD-2328238, AD-2328239, AD-2328240, AD- 2328241, AD-2328242, AD-2328243, AD-2328244, AD-2328246, AD-2328251, AD-2328252, AD- 2328253, AD-2328254, AD-2328255, AD-2328256, AD-2328257, AD-2328258, AD-2328266, AD- 2328374, AD-2328377, AD-2328576, AD-2328578, AD-2328579, AD-2328582, AD-2328583. AD- 2328585, AD-2328586, AD-2328637. AD-2328639, AD-2328640, AD-2328669, AD-2328670. AD- 2328839, AD-2328843, AD-2328844, AD-2328846, AD-2328859, AD-2328860, AD-2328937, AD- 2328942, AD-2328943, AD-2328944, AD-2328945, AD-2328946, AD-2328947, AD-2328948, AD- 2328949, AD-2328950, AD-2328979, AD-2329038, AD-2329044, AD-2329045, AD-2329046, AD- 2329047, AD-2329048, AD-2329050, AD-2329051, AD-2329052, AD-2329080, AD-2329081, AD- 2329082, AD-2329083, AD-2329084. AD-2329085, AD-2329143, AD-2329144, AD-2329145. AD- 2329147, AD-2329148, AD-2329149. AD-2329150, AD-2329151, AD-2329152, AD-2329153. AD- 2329154, AD-2329155, AD-2329156, AD-2329157, AD-2329158, AD-2329159, AD-2329160, AD- 2329161, AD-2329162, AD-2329163, AD-2329164, AD-2329165, AD-2329166, AD-2329168, AD- 2329173, AD-2329175, AD-2329176, AD-2329179, AD-2329180, AD-2329244, AD-2329245, AD- 2329248, AD-2329249, AD-2329253, AD-2329254, AD-2329255, AD-2329259, AD-2329260, AD- 2329263, AD-2329265, AD-2329268. AD-2329269, AD-2329271, AD-2329272, AD-2329273. AD- 2329274, AD-2329275, AD-2329276. AD-2329277, AD-2329278, AD-2329284, AD-2329285. AD- 2329373, AD-2329375, AD-2329376, AD-2329378, AD-2329379, AD-2329380, AD-2329381, AD- 2329382, AD-2329385, AD-2329386, AD-2329437, AD-2329438, AD-2329439, AD-2329440, AD- 2329444, AD-2329445, AD-2329446, AD-2329471, AD-2329475, AD-2329545, AD-2329546, AD- 2329550, AD-2329551, AD-2329554, AD-2329555, AD-2329557, AD-2329558, AD-2329562, AD- 2329563, AD-2329564, AD-2329565. AD-2329638, AD-2329639, AD-2329738, AD-2329739. AD- 2329740, AD-2329743, AD-2329744. AD-2329751, AD-2329752, AD-2329753. AD-2329754. AD- 2329755, AD-2329756, AD-2329757, AD-2329758, AD-2329759, AD-2329760, AD-2329761, AD- 2329762, AD-2329763, AD-2329769, AD-2329772, AD-2329839, AD-2329840, AD-2329841, AD- 2329878, AD-2329879, AD-2329880, AD-2329881, AD-2329882, AD-2329883, AD-2329884, AD- 2329885, AD-2329951, AD-2329952, AD-2330058, AD-2330059, AD-2330060, AD-2330061, AD- 2330062, AD-2330063, AD-2330065. AD-2330066, AD-2330071, AD-2330072, AD-2330075. AD- 2330077, AD-2330079, AD-2330156. AD-2330159, AD-2330160, AD-2330163. AD-2330164. AD- 2330165, AD-2330167, AD-2330168, AD-2330173, AD-2330176, AD-2330177, AD-2330179, AD- 2330180, AD-2330244, AD-2330245, AD-2330246, AD-2330247, AD-2330248, AD-2330249, AD- 2330250, AD-2330251, AD-2330252, AD-2330253, AD-2330254, AD-2330255, AD-2330256, AD- 2330257, AD-2330258, AD-2330259, AD-2330260, AD-2330261, AD-2330262, AD-2330263. AD- 2330267, AD-2330268, AD-2330269. AD-2330270, AD-2330271, AD-2330273, AD-2330342. AD- 2330343, AD-2330344, AD-2330345. AD-2330365, AD-2330368, AD-2330484. AD-2330510. AD- 2330515, AD-2330516, AD-2330517, AD-2330519, AD-2330520, AD-2330521, AD-2330532, AD- 2330533, AD-2330534, AD-2330536, AD-2330560, AD-2330563, AD-2330565, AD-2330573, AD- 2330574, AD-2330575, AD-2330596, AD-2330597, AD-2330598, AD-2330599, AD-2330600, AD- 2330601, AD-2330602, AD-2330603, AD-2330604, AD-2330605, AD-2330606, AD-2330607. AD- 2330608, AD-2330612, AD-2330613. AD-2330614, AD-2330615, AD-2330616, AD-2330618. AD- 2330619, AD-2330620, AD-2330623, AD-2330624, AD-2330625, AD-2330626, AD-2330627, AD- 2330628, AD-2330629, AD-2330630, AD-2330631, AD-2330632, AD-2330633, AD-2330634, AD- 2330638, AD-2330639, AD-2330640, AD-2330641, AD-2330644, AD-2330647, AD-2330648, AD- 2330649, AD-2330652, AD-2330653, AD-2330654, AD-2330655, AD-2330656, AD-2330657, AD- 2330658, AD-2330659, AD-2330671. AD-2330672, AD-2330673, AD-2330674, AD-2330675. AD- 2330679, AD-2330680, AD-2330681. AD-2330682, AD-2330683, AD-2330686, AD-2330691. AD- 2330698, AD-2330699, AD-2330700, AD-2330701, AD-2330702, AD-2330703, AD-2330704, AD- 2330705, AD-2330706, AD-2330707, AD-2330708, AD-2330709, AD-2330710, AD-2330711, AD- 2330712, AD-2330713, AD-2330714, AD-2330715, AD-2330716, AD-2330717, AD-2330720, AD- 2330722, AD-2330724, AD-2330736, AD-2330737, AD-2330738, AD-2330739, AD-2330740, AD- 2330741, AD-2330742, AD-2330743. AD-2330744, AD-2330745, AD-2330746, AD-2330747. AD- 2330752, AD-2330753, AD-2330754. AD-2330755, AD-2330756, AD-2330757, AD-2330759. AD- 2330760, AD-2330761, AD-2330762, AD-2330763, AD-2330764, AD-2330783, AD-2330785, AD- 2330821, AD-2330843, AD-2330844, AD-2330847, AD-2330849, AD-2330850, AD-2330851, AD- 2330855, AD-2330856, AD-2330873, AD-2330875, AD-2330877, AD-2330878, AD-2330880, AD- 2330881, AD-2330882, AD-2330883, AD-2330885, AD-2330887, AD-2330891, AD-2330892, AD- 2330897, AD-2330899, AD-2330901. AD-2330902, AD-2330903, AD-2330904, AD-2330905. AD- 2330906, AD-2330907, AD-2330908. AD-2330909, AD-2330915, AD-2330916. AD-2330917. AD- 2330918, AD-2330919, AD-2330920, AD-2330921, AD-2330922, AD-2330923, AD-2330924, AD- 2330933, AD-2330934, AD-2330935, AD-2330936, AD-2330938, AD-2330939, AD-2330940, and AD- 2330941.

[0092] In one embodiment, the dsRNA agent is selected from the group consisting of AD-2320882.1, AD-

[0093] 2320938.1, AD-2321352.1, AD-2321573.1, AD-2321665.1, AD-2321839.1, AD-2321863.1, AD-2322178.1, AD-2322257.1, AD-2322371.1, AD-2322980.1, AD-2323248.1, AD-2323253.1, AD-2323445.1, AD-

[0094] 2323482.1, AD-2323584.1, AD-2323585.1, AD-2323784.1, AD-2323856.1, AD-2323858.1, AD-2323886.1, AD-2323961.1, AD-2323965.1, AD-2323970.1, AD-2323972.1, AD-2323976.1, AD-2324043.1, AD-

[0095] 2324044.1, AD-2324046.1, AD-2324047.1, AD-2324276.1, AD-2324670.1, AD-2325059.1, AD-2325148.1, AD-2325356.1, AD-2325357.1, AD-2325369.1, AD-2325373.1, AD-2325448.1, AD-2325450.1, AD-

[0096] 2325473.1, AD-2325474.1, AD-2325477.1, AD-2325546.1, AD-2325552.1, AD-2325646.1, AD-2325648.1, AD-2325674.1, AD-2325677.1, AD-2325678.1. AD-2325679.1, AD-2325681.1, AD-2325744.1, AD-

[0097] 2325745.1, AD-2325746.1, AD-2325748.1, AD-2325752.1. AD-2325762.1, AD-2325763.1, AD-2325764.1, AD-2325765.1, AD-2325769.1, AD-2325780.1. AD-2325781.1, AD-2325782.1, AD-2325784.1, AD-

[0098] 2325785.1, AD-2325786.1, AD-2325837.1, AD-2325838.1. AD-2325839.1, AD-2325840.1, AD-2325847.1, AD-2325848.1, AD-2325955.1. AD-2325959.1. AD-2325968.1, AD-2325969.1, AD-2325973.1, AD- 2325976.1, AD-2325979.1, AD-2325984.1, AD-2326042.1, AD-2326067.1, AD-2326170.1, AD-2328140.1, AD-2328186.1, AD-2328257.1, AD-2328266.1, and AD-2328843.1.

[0099] In one embodiment, the dsRNA agent comprises at least one modified nucleotide.

[0100] In one embodiment, substantially all or all of the nucleotides of the sense strand comprise a modification. In another embodiment, substantially all or all of the nucleotides of the antisense strand comprise a modification. In yet another embodiment, substantially all or all of the nucleotides of the sense strand and substantially all or all of the nucleotides of the antisense strand comprise a modification.

[0101] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand and an antisense strand fanning a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides differing by no more than 1, 2, or 3 nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 1, 2, or 3 nucleotides from the nucleotide sequence of SEQ ID NO:2, wherein substantially all or all of the nucleotides of the sense strand and substantially all or all of the nucleotides of the antisense strand are modified nucleotides, and wherein the sense strand is conjugated to a ligand attached at the 3 '-terminus. In some embodiments, the dsRNA agent includes a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides from the nucleotide sequence of SEQ ID NO:2, wherein substantially all or all of the nucleotides of the sense strand and substantially all or all of the nucleotides of the antisense strand are modified nucleotides, and wherein the sense strand is conjugated to a ligand attached at the 3 '-terminus.

[0102] In one embodiment, all of the nucleotides of the sense strand comprise a modification. In another embodiment, all of the nucleotides of the antisense strand comprise a modification. In yet another embodiment, all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand comprise a modification.

[0103] In one embodiment, at least one of said modified nucleotides is selected from the group consisting of a deoxy -nucleotide, a 3 '-terminal deoxy-thymine (dT) nucleotide, a 2'-O-methyl modified nucleotide, a 2'-fluoro modified nucleotide, a 2'-deoxy-modified nucleotide, a locked nucleotide, an unlocked nucleotide, a confonnationally restricted nucleotide, a constrained ethyl nucleotide, an abasic nucleotide, a 2'-amino- modified nucleotide, a 2'-O-allyl-modified nucleotide, 2 '-C -alkyl -modified nucleotide, 2 '-hydroxyl -modified nucleotide, a 2' -methoxyethyl modified nucleotide, a 2 '-O-alkyl -modified nucleotide, a morpholino nucleotide, a phosphoramidate, a non-natural base comprising nucleotide, a tetrahydropyran modified nucleotide, a 1,5-anhydrohexitol modified nucleotide, a cyclohexenyl modified nucleotide, a nucleotide comprising a phosphorothioate group, a nucleotide comprising a methylphosphonate group, a nucleotide comprising a 5'-phosphate, a nucleotide comprising a 5'-phosphate mimic, a glycol modified nucleotide, and a 2-0-(N-methylacetamide) modified nucleotide, and combinations thereof.

[0104] In one embodiment, the nucleotide modifications are 2'-O-methyl and / or 2 '-fluoro modifications.

[0105] Tire region of complementarity may be at least 17 nucleotides in length; 19 to 30 nucleotides in length; 19-25 nucleotides in length; or 21 to 23 nucleotides in length.

[0106] Each of the sense and antisense strands may be no more than 30 nucleotides in length, e.g., each of the sense and antisense strands is independently 19-30 nucleotides in length; each of the sense and antisense strands is independently 19-25 nucleotides in length; each of the sense and antisense strands is independently 21-23 nucleotides in length. Tire dsRNA may include at least one of the sense or antisense strands that comprises a 3' overhang of at least 1 nucleotide: or at least one of the sense or antisense strands that comprises a 3' overhang of at least 2 nucleotides.

[0107] In some embodiment, the dsRNA agent further comprises a ligand.

[0108] In one embodiment, the ligand is conjugated to the 3' end of the sense strand of the dsRNA agent. In one embodiment, the ligand is an N -acetylgalactosamine (GalNAc) derivative.

[0109] In one embodiment, the ligand is

[0110] In one embodiment, the dsRNA agent is conjugated to the ligand as shown in the following schematic and, wherein X is O or S.

[0111] In one embodiment, the X is 0.

[0112] In one embodiment, the region of complementarity comprises any one of the antisense sequences in Tables 3-6.

[0113] In one aspect, the present invention provides a double stranded for inhibiting expression of Aminoadipate -semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand complementary to an antisense strand, wherein the antisense strand comprises a region complementary to part of an mRNA encoding AASS, wherein each strand is about 14 to about 30 nucleotides in length, wherein said dsRNA agent is represented by formula (Ij): sense: 5' np-Na-(X X);-Nb-Y Y Y -Nb-(Z Z Z)j -Na- nq3' antisense: 3' np'-Na'-(X'X'X')k-Nb'-Y'Y'Y'-Nb'-(Z'Z'Z')i-Na'- nq' 5' (Ij) wherein: i, j, k, and 1 are each independently 0 or 1; p, p', q, and q' are each independently 0-6; each Naand Na' independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotides; each Nband Nb' independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof; each np, np', nq, and nq', each of which may or may not be present, independently represents an overhang nucleotide;

[0114] XXX, YYY, ZZZ, X'X'X', Y'Y'Y', and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides; modifications on Nbdiffer from the modification on Y and modifications on Nb' differ from the modification on Y' ; and wherein the sense strand is conjugated to at least one ligand.

[0115] In one embodiment, i is 0; j is 0; i is 1 ; j is 1 ; both i and j are 0; or both i and j are 1. In another embodiment, k is 0; 1 is 0; k is 1; 1 is 1; both k and 1 are 0; or both k and 1 are 1.

[0116] In one embodiment. XXX is complementary to X'X'X', YYY is complementary to Y'Y'Y', and ZZZ is complementary to Z'Z'Z'.

[0117] In one embodiment, the YYY motif occurs at or near the cleavage site of the sense strand, e.g., the Y'Y'Y' motif occurs at the 11, 12 and 13 positions of the antisense strand from the 5'-end.

[0118] In one embodiment, formula (Ij) is represented by formula (Ik): sense: 5' np-Na-Y Y Y -Na- nq3' antisense: 3' nP'-Na'- Y'Y'Y'- Na~ nq' 5' (Ik). In another embodiment, formula (Ij) is represented by formula (II): sense: 5' np-Na-Y Y Y -Nb-Z Z Z -Na- nq3' antisense: 3' np-Na- Y'Y'Y'-Nb-Z'Z'Z'- Na- nq, 5' (II) wherein each Nband Nb' independently represents an oligonucleotide sequence comprising 1-5 modified nucleotides.

[0119] In yet another embodiment, formula (Ij) is represented by formula (Im): sense: 5' nP-Na-X X X -Nb-Y Y Y -Na- nq3' antisense: 3' np-Na- X'X'X'-Nb- Y'Y'Y'- Na- nq, 5' (Im) wherein each Nband Nb' independently represents an oligonucleotide sequence comprising 1-5 modified nucleotides.

[0120] In another embodiment, formula (Ij) is represented by formula (In): sense: 5' np-Na-X X X- Nb-Y Y Y -Nb-Z Z Z -Na- nq3' antisense: 3' nP-Na- X'X'X'- Nb-Y'Y'Y'-Nb-Z'Z'Z'- Na- ncf5' (In) wherein each Nband Nb' independently represents an oligonucleotide sequence comprising 1-5 modified nucleotides and each Naand Na' independently represents an oligonucleotide sequence comprising 2- 10 modified nucleotides.

[0121] The region of complementarity may be at least 17 nucleotides in length: 19 to 30 nucleotides in length; 19-25 nucleotides in length; or 21 to 23 nucleotides in length.

[0122] Each strand may be no more than 30 nucleotides in length, e.g., each strand is independently 19-30 nucleotides in length.

[0123] In one embodiment, the modifications on the nucleotides are selected from the group consisting of LNA, HNA. CeNA, 2'-methoxyethyl, 2'-O-alkyl, 2'-O-allyl, 2'-C- allyl, 2'-fluoro, 2'-O-methyl, 2'-deoxy, 2'- hydroxyl, and combinations thereof.

[0124] In one embodiment, the modifications on the nucleotides are 2'-O-methyl or 2'-fluoro modifications.

[0125] In one embodiment, the Y' is a 2'-O-methyl or 2'-flouro modified nucleotide.

[0126] In one embodiment, at least one of the sense or antisense strands of the dsRNA agent may comprise a 3‘ overhang of at least 1 nucleotide; or a 3' overhang of at least 2 nucleotides.

[0127] In one embodiment, the dsRNA agent further comprises at least one phosphorothioate or methylphosphonate intemucleotide linkage.

[0128] In one embodiment, the phosphorothioate or methylphosphonate intemucleotide linkage is at the 3'- terminus of one strand. In one embodiment, the strand is the antisense strand. In another embodiment, the strand is the sense strand.

[0129] In one embodiment, the phosphorothioate or methylphosphonate intemucleotide linkage is at the 5'- terminus of one strand. In one embodiment, the strand is the antisense strand. In another embodiment, the strand is the sense strand. In one embodiment, the strand is the antisense strand. In another embodiment, the strand is the sense strand.

[0130] In one embodiment, tire phosphorothioate or methylphosphonate intemucleotide linkage is at both the 5'- and 3 '-terminus of one strand.

[0131] In one embodiment, the base pair at the 1 position of the 5 '-end of the antisense strand of the duplex is an AU base pair.

[0132] In one embodiment, p'>0. In another embodiment, p'=2.

[0133] In one embodiment, q'=0, p=0, q=0, and p' overhang nucleotides are complementary to tire target mRNA. In another embodiment, q'=0, p=0, q=0, and p‘ overhang nucleotides are non-complementary to the target mRNA.

[0134] In one embodiment, the sense strand has a total of 21 nucleotides and the antisense strand has a total of 23 nucleotides.

[0135] In one embodiment, at least one np' is linked to a neighboring nucleotide via a phosphorothioate linkage. In another embodiment, wherein all np' are linked to neighboring nucleotides via phosphorothioate linkages.

[0136] In one embodiment, all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand comprise a modification.

[0137] In one embodiment, the ligand is conjugated to the 3' end of the sense strand of the dsRNA agent.

[0138] In one embodiment, the ligand is one or more N-acetylgalactosamine (GalNAc) derivatives attached through a monovalent, bivalent, or trivalent branched linker.

[0139] In one embodiment, the ligand is

[0140] In one embodiment, the dsRNA agent is conjugated to the ligand as shown in the following schematic

[0141] and. wherein X is O or S.

[0142] In one embodiment, the X is 0.

[0143] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand complementary to an antisense strand, wherein the antisense strand comprises a region complementary to part of an mRNA encoding AASS, wherein each strand is about 14 to about 30 nucleotides in length, wherein the dsRNA agent is represented by formula (Ij): sense: 5' nP-Na-(X X X)t-Nb-Y Y Y -Nb-(Z Z Z)j -Na- nq3' antisense: 3' np'-Na'-(X'X'X')k-Nb'-Y'Y'Y'-Nb'-(Z'Z'Z')i-Na'- nq' 5' (Ij) wherein: i, j, k, and 1 are each independently 0 or 1; p, p', q, and q' are each independently 0-6; each Naand Na' independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotides; each Nband Nb' independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof; each np, np', nq, and nq', each of which may or may not be present independently represents an overhang nucleotide;

[0144] XXX, YYY, ZZZ, X'X'X', Y'YY', and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides, and wherein the modifications are 2'-O-methyl or 2'- fluoro modifications; modifications on Nbdiffer from the modification on Y and modifications on Nb' differ from the modification on Y'; and wherein the sense strand is conjugated to at least one ligand. In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand complementary to an antisense strand, wherein the antisense strand comprises a region complementary to part of an rnRNA encoding AASS, wherein each strand is about 14 to about 30 nucleotides in length, wherein the dsRNA agent is represented by formula (Ij): sense: 5' np-Na-(X X X) i-Nb-Y Y Y -Nb-(Z Z Z)j -Na- nq3' antisense: 3' nP'-Na'-(X'X'X')k-Nb'-Y'Y'Y'-Nb'-(Z'Z'Z')i-Na'- nq' 5' (Ij) wherein: i, j, k, and 1 are each independently 0 or 1; each np, nq, and nq', each of which may or may not be present, independently represents an overhang nucleotide; p, q. and q' are each independently 0-6; np' >0 and at least one np' is linked to a neighboring nucleotide via a phosphorothioate linkage: each Naand Na' independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotides; each Nband Nb' independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof:

[0145] XXX, YYY, ZZZ , X'X'X' , Y'Y'Y', and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides, and wherein the modifications are 2'-O-methyl or 2'- fluoro modifications; modifications on Nbdiffer from the modification on Y and modifications on Nb' differ from the modification on Y'; and wherein the sense strand is conjugated to at least one ligand.

[0146] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand complementary to an antisense strand, wherein the antisense strand comprises a region complementary to part of an mRNA encoding AASS, wherein each strand is about 14 to about 30 nucleotides in length, wherein the dsRNA agent is represented by formula (Ij): sense: 5' nP-Na-(X X X) i-Nb-Y Y Y -Nb-(Z Z Z)j -Na- nq3' antisense: 3' np'-Na'-(X'X'X')k-Nb'-Y'Y'Y'-Nb'-(Z'Z'Z')i-Na'- nq' 5' (Ij) wherein: i, j, k, and 1 are each independently 0 or 1; each np, nq, and nq', each of which may or may not be present, independently represents an overhang nucleotide; p, q, and q' are each independently 0-6; np' >0 and at least one np' is linked to a neighboring nucleotide via a phosphorothioate linkage; each Naand Na' independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotides; each Nb and Nb' independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof;

[0147] XXX, YYY, ZZZ , X'X'X', Y'Y'Y', and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides, and wherein the modifications arc 2'-O-mcthyl or 2'- fluoro modifications; modifications on Nb differ from the modification on Y and modifications on Nb' differ from the modification on Y'; and wherein the sense strand is conjugated to at least one ligand, wherein the ligand is one or more GalNAc derivatives attached through a monovalent, bivalent, or trivalent branched linker.

[0148] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand complementary to an antisense strand, wherein the antisense strand comprises a region complementary to part of an mRNA encoding AASS, wherein each strand is about 14 to about 30 nucleotides in length, wherein the dsRNA agent is represented by formula (Ij): sense: 5' np-Na-(X X X)i-Nb-Y Y Y -Nb-(Z Z Z)j -Na- nq3' antisense: 3' np'-Na'-(X'X'X')k-Nb'-Y'Y'Y'-Nb'-(Z'Z'Z')i-Na'- nq' 5' (Ij) wherein: i, j, k, and 1 are each independently 0 or 1; each np, nq, and nq', each of which may or may not be present, independently represents an overhang nucleotide; p, q, and q' are each independently 0-6; np' >0 and at least one np' is linked to a neighboring nucleotide via a phosphorothioate linkage; each Naand Na' independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotides; each Nband Nb' independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or umnodified or combinations thereof;

[0149] XXX, YYY, ZZZ , X'X'X', Y'Y'Y', and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides, and wherein the modifications are 2'-O-methyl or 2'- fluoro modifications; modifications on Nb differ from the modification on Y and modifications on Nb' differ from the modification on Y'; wherein the sense strand comprises at least one phosphorothioate linkage; and wherein the sense strand is conjugated to at least one ligand, wherein the ligand is one or more GalNAc derivatives attached through a monovalent, bivalent, or trivalent branched linker.

[0150] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. The dsRNA agent includes a sense strand complementary to an antisense strand, wherein the antisense strand comprises a region complementary to part of an mRNA encoding AASS, wherein each strand is about 14 to about 30 nucleotides in length, wherein tire dsRNA agent is represented by formula (Ij): sense: 5' np-Na-Y Y Y - Na- nq3' antisense: 3' np'-Na'- Y'Y'Y'- Na'- nq' 5' (Ik) wherein: each np, nq, and nq', each of which may or may not be present, independently represents an overhang nucleotide; p, q. and q' are each independently 0-6; np' >0 and at least one np' is linked to a neighboring nucleotide via a phosphorothioate linkage; each Naand Na' independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotides;

[0151] YYY and Y'Y'Y' each independently represent one motif of three identical modifications on three consecutive nucleotides, and wherein the modifications are 2'-O-methyl and / or 2'-fluoro modifications; wherein the sense strand comprises at least one phosphorothioate linkage; and wherein the sense strand is conjugated to at least one ligand, wherein the ligand is one or more GalNAc derivatives attached through a monovalent, bivalent, or trivalent branched linker.

[0152] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate-semialdehyde synthase (AASS) in a cell. Tire dsRNA agent includes a sense strand and an antisense strand fonning a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides differing by no more than 1, 2. or 3 nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 1, 2, or 3 nucleotides from the nucleotide sequence of SEQ ID NO:2, wherein substantially all or all of the nucleotides of the sense strand comprise a modification selected from the group consisting of a 2'-O-methyl modification and a 2 '-fluoro modification, wherein the sense strand comprises two phosphorothioate intemucleotide linkages at the 5 '-terminus, wherein substantially all or all of the nucleotides of the antisense strand comprise a modification selected from the group consisting of a 2 -0- methyl modification and a 2 '-fluoro modification, wherein the antisense strand comprises two phosphorothioate intemucleotide linkages at the 5 '-terminus and two phosphorothioate intemucleotide linkages at the 3'-terminus, and wherein the sense strand is conjugated to one or more GalNAc derivatives attached through a monovalent, bivalent or trivalent branched linker at the 3'-tenninus. In some embodiments, the dsRNA agent includes a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides from the nucleotide sequence of SEQ ID NO:2, wherein substantially all or all of the nucleotides of the sense strand comprise a modification selected from the group consisting of a 2'-O-methyl modification and a 2 '-fluoro modification, wherein the sense strand comprises two phosphorothioate intemucleotide linkages at the 5 '-terminus, wherein substantially all or all of the nucleotides of the antisense strand comprise a modification selected from the group consisting of a 2'-O-methyl modification and a 2'-fluoro modification, wherein tire antisense strand comprises two phosphorothioate intemucleotide linkages at the 5 '-terminus and two phosphorothioate intemucleotide linkages at the 3 '-terminus, and wherein the sense strand is conjugated to one or more GalNAc derivatives attached through a monovalent, bivalent or trivalent branched linker at the 3 '-terminus.

[0153] In one embodiment, all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand are modified nucleotides.

[0154] In one embodiment, the region of complementarity comprises any one of the antisense sequences listed in Tables 3-6.

[0155] In one embodiment, the sense strand and the antisense strand comprise nucleotide sequences selected from the group consisting of the nucleotide sequences of any one of tire agents listed in Tables 3-6.

[0156] In various embodiments of the aforementioned dsRNA agents, tire dsRNA agent targets a hotspot region of an mRNA encoding AASS.

[0157] In another aspect, the present invention provides a dsRNA agent that targets a hotspot region of a Aminoadipate-semialdehyde synthase (AASS) mRNA.

[0158] The present invention also provides cells, vectors, and pharmaceutical compositions which include any of the dsRNA agents of the invention. The dsRNA agents may be formulated in an unbuffered solution, e.g., saline or water, or in a buffered solution, e.g., a solution comprising acetate, citrate, prolamine, carbonate, or phosphate or any combination thereof. In one embodiment, the buffered solution is phosphate buffered saline (PBS).

[0159] In one aspect, the present invention provides a method of inhibiting Aminoadipate-semialdehyde synthase (AASS) expression in a cell. The method includes contacting the cell with a dsRNA agent or a pharmaceutical composition of the invention, thereby inhibiting expression of AASS in the cell.

[0160] The cell may be within a subject, such as a human subject. In one embodiment, the AASS expression is inhibited by at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or to below the level of detection of AASS expression.

[0161] In one embodiment, the human subject suffers from an AASS-associated disease, disorder, or condition. In one embodiment, the AASS-associated disease, disorder, or condition is a lysine catabolism disorder. In one embodiment, the lysine catabolism disorder is glutaric aciduria type 1 (GAI). In one embodiment, the lysine catabolism disorder is pyridoxine-dependent epilepsy (PDE).

[0162] In one aspect, the present invention provides a method of inhibiting the expression of AASS in a subject. The methods include administering to the subject a therapeutically effective amount of a dsRNA agent or a pharmaceutical composition of the invention, thereby inhibiting the expression of AASS in the subject.

[0163] In another aspect, the present invention provides a method of treating a subject suffering from an AASS-associated disease, disorder, or condition. The method includes administering to the subject a therapeutically effective amount of a dsRNA agent or a pharmaceutical composition of the invention, thereby treating the subject suffering from an AASS-associated disease, disorder, or condition.

[0164] In another aspect, the present invention provides a method of preventing at least one symptom in a subject having a disease, disorder or condition that would benefit from reduction in expression of an AASS gene. The method includes administering to the subject a prophylactically effective amount of the agent of a dsRNA agent or a pharmaceutical composition of the invention, thereby preventing at least one symptom in a subject having a disease, disorder or condition that would benefit from reduction in expression of an AASS gene.

[0165] In one embodiment, the administration of the dsRNA agent or the pharmaceutical composition to the subject causes a decrease in AASS protein activity, e.g., a decrease in the production of saccharopine and / or 2- aminoadipic-4-semialdehyde; a decrease in AASS protein accumulation, a decrease in AASS enzymatic activity, a decrease in the accumulation of glutaric acid and / or 3 -hydroxy-glutaric acid in a subject, and / or a decrease in alpha-aminoadipic semialdehyde (a-AASA) in urine and / or plasma.

[0166] In one embodiment, the AASS-associated disease, disorder, or condition is a lysine catabolism disorder.

[0167] In one embodiment, the lysine catabolism disorder is glutaric aciduria type 1 (GAI).

[0168] In one embodiment, the lysine catabolism disorder is pyridoxine-dependent epilepsy (PDE).

[0169] In one embodiment, the methods and uses of the invention further include administering an additional therapeutic to the subject.

[0170] In one embodiment, the dsRNA agent is administered to the subject at a dose of about 0.01 mg / kg to about 10 mg / kg or about 0.5 mg / kg to about 50 mg / kg.

[0171] The agent may be administered to the subject intravenously, intramuscularly, or subcutaneously. In one embodiment, the agent is administered to the subject subcutaneously. In one embodiment, the methods and uses of the invention further include determining, the level of AASS in the subject.

[0172] In one aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of Aminoadipate -semialdehyde synthase (AASS) in a cell, wherein the dsRNA agent comprises a sense strand and an antisense strand fonning a double stranded region, wherein the sense strand comprises a nucleotide sequence of any one of the agents in any one of Tables 3-6 and the antisense strand comprises a nucleotide sequence of any one of the agents in any one of Tables 3-6, wherein substantially all or all of the nucleotide of the sense strand and substantially all or all of tire nucleotides of the antisense strand are modified nucleotides, and wherein the dsRNA agent is conjugated to a ligand.

[0173] DETAILED DESCRIPTION OF THE INVENTION

[0174] The present invention provides iRNA compositions, which effect the RNA-induced silencing complex (RlSC)-mediated cleavage of RNA transcripts of an AASS gene. Tire AASS gene may be within a cell, e.g.. a cell within a subject, such as a human. The present invention also provides methods of using the iRNA compositions of the invention for inhibiting the expression of an AASS gene, and for treating a subject w ho would benefit from inhibiting or reducing the expression of an AASS gene, e.g., a subject suffering or prone to suffering from an AASS-associated disease disorder, or condition, such as a subject suffering or prone to suffering from lysine catabolism disorders, e.g.. a subject suffering from glutaric aciduria type 1 (GAI) or pyridoxine-dependent epilepsy (PDE).

[0175] The saccharopine pathw ay of lysine catabolism is primarily localized to liver mitochondria and is the major pathway of lysine catabolism in humans. Aminoadipate-semialdehyde synthase (AASS) is a dual function enzyme involved in the catabolism of lysine in the first two steps of the saccharopine pathway. The lysine-ketoglutarate reductase function of AASS breaks down lysine to saccharopine and. in the second step, the saccharopine dehydrogenase function converts saccharopine to alpha-aminoadipic semialdehyde. The next reaction in the pathway is the conversion of alpha-aminoadipic semialdehyde to a-aminoadipic acid by a-aminoadipic semialdehyde dehydrogenase (ALDH7A1). This is followed by production of 2-ketoadipic acid and finally conversion of 2-ketoadipic acid to glutaryl-CoA. Ghitaryl- CoA is converted to crotonyl-CoA by Glutaryl-CoA dehydrogenase (GCDH). Inhibition of the conversion of glutaryl-CoA to crotonyl-CoA can lead to the production and accumulation of toxic catabolites such as glutaric acid and 3 -hydroxy-glutaric acid. Disruptions in the lysine catabolism pathway, such as deficiencies in any of the enzymes, can result in various lysine catabolism disorders including glutaric aciduria type 1 (GAI) and pyridoxine-dependent epilepsy (PDE). GAI results from deficiency in GCDH which leads to accumulation of toxic byproducts of glutaryl-CoA. Deficiency of ALDH7A1 leads to accumulation of alpha-aminoadipic semialdehyde and L-Pipecolic acid and the development of PDE. AASS is upstream of both ALDH7A1 and GCDH in the lysine catabolism pathway. Inhibiting or reducing expression of AASS could result in decreased accumulation of metabolites. GCDH knockout mice have a GAI phenotype and are used as a model to study GAI . GCDH / AASS double knockout mice have improved survival with reduced levels of tire toxic metabolite glutaric acid and reduced GAI phenotype (Barzi et al. 2023, Sci. Transl. Med. 15(692):eadf4086: and Leandro et al., 2020, J. Inherited metabolic Disease, 43: 1154-64, which are incorporated herein by reference). Transplantation of GCDH / AASS+ / +hepatocytes into GCDH / AASS double knockout mice resulted in the return of the GAI phenotype (Barzi et al. 2023, Sci. Transl. Med. 15(692):eadf4086). Accordingly, AASS represents a target for treating lysine catabolism disorders with tire dsRNA agents provided herein.

[0176] The iRNAs of tire invention targeting AASS may include an RNA strand (tire antisense strand) having a region which is about 30 nucleotides or less in length, e.g., 15-30, 15-29, 15-28, 15-27, 15-26. 15-25, 15-24. 15-23. 15-22, 15-21. 15-20, 15-19, 15-18, 15-17, 18-30. 18-29, 18-28. 18-27, 18-26, 18-25, 18-24, 18-23. 18-

[0177] 22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24,20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-

[0178] 23, or 21-22 nucleotides in length, which region is substantially complementary to at least part of an mRNA transcript of an AASS gene.

[0179] In some embodiments, one or both of the strands of the double stranded RNAi agents of tire invention is up to 66 nucleotides in length, e.g., 36-66. 26-36, 25-36, 31-60. 22-43, 27-53 nucleotides in length, with a region of at least 19 contiguous nucleotides that is substantially complementary to at least a part of an mRNA transcript of an AASS gene. In some embodiments, such iRNA agents having longer length antisense strands may include a second RNA strand (the sense strand) of 20-60 nucleotides in length wherein the sense and antisense strands form a duplex of 18-30 contiguous nucleotides.

[0180] The use of tire iRNA agents described herein enables the targeted degradation of mRNAs of an AASS gene in mammals.

[0181] Very low dosages of the iRNAs, in particular, can specifically and efficiently mediate RNA interference (RNAi), resulting in significant inhibition of expression of an AASS gene. Thus, methods and compositions including these iRNAs are useful for treating a subject who would benefit from inhibiting or reducing the expression of an AASS gene, e.g., a subject suffering or prone to suffering from an AASS- associated disease disorder, or condition, such as a subject suffering or prone to suffering from lysine catabolism disorders, e.g.. a subject suffering from glutaric aciduria type 1 (GAI) or pyridoxine -dependent epilepsy (PDE).

[0182] The following detailed description discloses how to make and use compositions containing iRNAs to inhibit the expression of an AASS gene, as well as compositions and methods for treating subjects having diseases and disorders that would benefit from inhibition and / or reduction of the expression of this gene. I. Definitions

[0183] In order that the present invention may be more readily understood, certain terms are first defined. In addition, it should be noted that whenever a value or range of values of a parameter are recited, it is intended that values and ranges intermediate to the recited values are also intended to be part of this invention.

[0184] The articles “a” and “an” are used herein to refer to one or to more than one (i. e. , to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element, e.g., a plurality of elements.

[0185] The term "including" is used herein to mean, and is used interchangeably with, the phrase "including but not limited to".

[0186] Tire tenn "or" is used herein to mean, and is used interchangeably with, tire temr "and / or," unless context clearly indicates otherwise.

[0187] The term “about” is used herein to mean within the typical ranges of tolerances in the art. For example, “about” can be understood as about 2 standard deviations from the mean. In certain embodiments, about means +10%. In certain embodiments, about means +5%. When about is present before a series of numbers or a range, it is understood that “about” can modify each of the numbers in the series or range.

[0188] The term “AASS,” also known as “Aminoadipate-semialdehyde synthase”, “alpha-aminoadipate semialdehyde synthase”, “aminoadipic semialdehyde synthase”, “a-aminoadipate semialdehyde dehydrogenase (AASADH)”, “lysine-2-oxoglutarate reductase”, or “lysine-ketoglutarate reductase / saccharopine dehydrogenase”, refers to the well-known gene encoding an AASS protein from any vertebrate or mammalian source, including, but not limited to, human, bovine, chicken, rodent, mouse, rat, porcine, ovine, primate, monkey, and guinea pig, unless specified otherwise.

[0189] The term also refers to fragments and variants of native AASS that maintain at least one in vivo or in vitro activity of a native AASS.

[0190] Exemplary nucleotide and amino acid sequences of AASS can be found, for example, at GenBank Accession No. NM 005763.4 (SEQ ID NO: 1 : reverse complement SEQ ID NO: 2) for Homo sapiens.

[0191] Exemplary nucleotide and amino acid sequences of AASS can be found, for example, at GenBank Accession No. NM_013930.4 (SEQ ID NO: 3; reverse complement SEQ ID NO: 4) for Mus musculus.

[0192] Exemplary nucleotide and amino acid sequences of AASS can be found, for example, at GenBank Accession No. NM 001100963.1 (SEQ ID NO: 5; reverse complement SEQ ID NO: 6) for Rattus norvegicus.

[0193] Exemplary nucleotide and amino acid sequences of AASS can be found, for example, at GenBank Accession No. XM 005550630.2 (SEQ ID NO: 9311; reverse complement SEQ ID NO: 9312) for Macaca fascicularis.

[0194] Additional examples of AASS mRNA sequences arc readily available using publicly available databases, e.g., GenBank, UniProt, and OMIM. Further information on AASS is provided, for example in the NCBI Gene database at http : / / www .ncbi .nlm .nih .gov / gene / 10157.

[0195] In some embodiments, the iRNAs that are substantially complementary to a region of a mouse or rat AASS rnRNA cross-react with human AASS mRNA and represent potential candidates for human targeting.

[0196] The term “AASS” as used herein also refers to a particular polypeptide expressed in a cell by naturally occurring DNA sequence variations of the AASS gene, such as a single nucleotide polymorphism in tire AASS gene. Numerous Single Nucleotide Polymorphisms (SNPs) within the AASS gene have been identified and may be found at, for example, NCBI dbSNP (see, e.g.. www.ncbi.nlm.nih.gov / snp).

[0197] As used herein, “target sequence” refers to a contiguous portion of the nucleotide sequence of an mRNA molecule fanned during tire transcription of an AASS gene, including mRNA that is a product of RNA processing of a primary transcription product. In one embodiment, the target portion of the sequence will be at least long enough to serve as a substrate for iRNA-directed cleavage at or near that portion of the nucleotide sequence of an mRNA molecule formed during the transcription of an AASS gene.

[0198] The target sequence of an AASS gene may be from about 9-36 nucleotides in length, e.g., about 15-30 nucleotides in length. For example, the target sequence can be from about 15-30 nucleotides, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-

[0199] 26, 18-25, 18-24, 18-23. 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25. 19-24, 19-23, 19-22, 19-21. 19-20, 20-30. 20-29, 20-28, 20-27. 20-26, 20-25. 20-24,20-23. 20-22, 20-21. 21-30, 21-29. 21-28, 21-

[0200] 27, 21-26, 21-25, 21-24, 21-23, or 21-22 nucleotides in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the invention.

[0201] As used herein, the term “strand comprising a sequence” refers to an oligonucleotide comprising a chain of nucleotides that is described by the sequence referred to using the standard nucleotide nomenclature.

[0202] “G,” “C,” “A,” “T” and “U” each generally stand for a nucleotide that contains guanine, cytosine, adenine, thymidine and uracil as a base, respectively. However, it will be understood that the term “ribonucleotide” or “nucleotide” can also refer to a modified nucleotide, as further detailed below, or a surrogate replacement moiety (see, e.g., Table 2). The skilled person is well aware that guanine, cytosine, adenine, and uracil can be replaced by other moieties without substantially altering the base pairing properties of an oligonucleotide comprising a nucleotide bearing such replacement moiety. For example, without limitation, a nucleotide comprising inosine as its base can base pair with nucleotides containing adenine, cytosine, or uracil. Hence, nucleotides containing uracil, guanine, or adenine can be replaced in the nucleotide sequences of dsRNA featured in the invention by a nucleotide containing, for example, inosine. In another example, adenine and cytosine anywhere in the oligonucleotide can be replaced with guanine and uracil, respectively to form G-U Wobble base pairing with the target mRNA. Sequences containing such replacement moieties are suitable for the compositions and methods featured in the invention. The terms “iRNA”, '‘RNAi agent,'' “iRNA agent,”, “RNA interference agent” as used interchangeably herein, refer to an agent that contains RNA as that term is defined herein, and which mediates the targeted cleavage of an RNA transcript via an RNA-induced silencing complex (RISC) pathway. iRNA directs the sequence-specific degradation of mRNA through a process known as RNA interference (RNAi). The iRNA modulates, e.g., inhibits, the expression of AASS gene in a cell, e.g., a cell within a subject, such as a mammalian subject.

[0203] In one embodiment, an RNAi agent of the invention includes a single stranded RNA that interacts with a target RNA sequence, e.g., an AASS target mRNA sequence, to direct the cleavage of the target RNA. Without wishing to be bound by theory it is believed that long double stranded RNA introduced into cells is broken down into siRNA by a Type III endonuclease known as Dicer (Sharp et al. (2001) Genes Dev. 15:485). Dicer, a ribonuclease -Ill-like enzyme, processes the dsRNA into 19-23 base pair short interfering RNAs with characteristic two base 3' overhangs (Bernstein, et al.. (2001) Nature 409:363). The siRNAs are then incorporated into an RNA-induced silencing complex (RISC) where one or more helicases unwind the siRNA duplex, enabling the complementary antisense strand to guide target recognition (Nykanen, et al., (2001) Cell 107:309). Upon binding to the appropriate target mRNA, one or more endonucleases within the RISC cleave the target to induce silencing (Elbashir, et al., (2001) Genes Dev. 15: 188). Thus, in one aspect the invention relates to a single stranded RNA (sssiRNA) generated within a cell and which promotes the formation of a RISC complex to effect silencing of the target gene. i.e.. an AASS gene. Accordingly, the term "‘siRNA” is also used herein to refer to an RNAi as described above.

[0204] In another embodiment, the RNAi agent may be a single-stranded RNAi agent that is introduced into a cell or organism to inhibit a target mRNA. Single-stranded RNAi agents (ssRNAi) bind to the RISC endonuclease, Argonaute 2, which then cleaves the target mRNA. Tire single -stranded siRNAs are generally 15-30 nucleotides and are chemically modified. The design and testing of single-stranded RNAi agents are described in U.S. Patent No. 8,101,348 and in Tima et al.. (2012) Cell 150: 883-894, the entire contents of each of which are hereby incorporated herein by reference. Any of the antisense nucleotide sequences described herein may be used as a single -stranded siRNA as described herein or as chemically modified by the methods described in Lima et al., (2012) Cell 150; 883-894.

[0205] In another embodiment, an “iRNA” for use in the compositions and methods of the invention is a double -stranded RNA and is referred to herein as a “double stranded RNAi agent,” “double-stranded RNA (dsRNA) molecule,” “dsRNA agent,” or “dsRNA”. The term “dsRNA”, refers to a complex of ribonucleic acid molecules, having a duplex structure comprising two anti-parallel and substantially complementary nucleic acid strands, referred to as having “sense” and “antisense” orientations with respect to a target RNA, i.e., an AASS gene. In some embodiments of the invention, a double -stranded RNA (dsRNA) triggers the degradation of a target RNA, e.g., an mRNA, through a post-transcriptional gene-silencing mechanism referred to herein as RNA interference or RNAi. In general, the majority of nucleotides of each strand of a dsRNA molecule are ribonucleotides, but as described in detail herein, each or both strands can also include one or more non-ribonucleotides, e.g., a deoxyribonucleotide and / or a modified nucleotide. In addition, as used in this specification, an "RNAi agent" may include ribonucleotides with chemical modifications; an RNAi agent may include substantial modifications at multiple nucleotides. As used herein, the term “modified nucleotide" refers to a nucleotide having, independently, a modified sugar moiety, a modified intemucleotide linkage, and / or a modified nucleobase. Thus, the term modified nucleotide encompasses substitutions, additions or removal of, e.g.. a functional group or atom, to intemucleotide linkages, sugar moieties, or nucleobases. The modifications suitable for use in the agents of the invention include all types of modifications disclosed herein or known in the art. Any such modifications, as used in a siRNA type molecule, are encompassed by “RNAi agent” for the purposes of this specification and claims.

[0206] The duplex region may be of any length that permits specific degradation of a desired target RNA through a RISC pathway, and may range from about 9 to 36 base pairs in length, e.g., about 15-30 base pairs in length, for example, about 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, or 36 base pairs in length, such as about 15-30, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-

[0207] 22, 18-21, 18-20, 19-30. 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21. 19-20, 20-30, 20-29, 20-28. 20-27, 20-26. 20-25, 20-24,20-23, 20-22. 20-21, 21-30, 21-29, 21-28, 21-27. 21-26, 21-25. 21-24, 21-

[0208] 23, or 21-22 base pairs in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the invention.

[0209] Tire two strands forming the duplex structure may be different portions of one larger RNA molecule, or they may be separate RNA molecules. Where the two strands are part of one larger molecule, and therefore are connected by an uninterrupted chain of nucleotides between the 3 '-end of one strand and the 5 '-end of the respective other strand forming the duplex structure, the connecting RNA chain is referred to as a “hairpin loop.” A hairpin loop can comprise at least one unpaired nucleotide. In some embodiments, the hairpin loop can comprise at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 20, at least 23 or more unpaired nucleotides.

[0210] Where tire two substantially complementary strands of a dsRNA are comprised by separate RNA molecules, those molecules need not, but can be covalently connected. Where the two strands are connected covalently by means other than an uninterrupted chain of nucleotides between the 3 '-end of one strand and the 5 '-end of the respective other strand forming the duplex structure, the connecting structure is referred to as a “linker”. The RNA strands may have the same or a different number of nucleotides. The maximum number of base pairs is the number of nucleotides in the shortest strand of the dsRNA minus any overhangs that arc present in the duplex. In addition to the duplex structure, an RNAi may comprise one or more nucleotide overhangs. In one embodiment, an RNAi agent of the invention is a dsRNA, each strand of which comprises less than 30 nucleotides, e.g.. 17-27, 19-27, 17-25, 19-25, or 19-23, that interacts with a target RNA sequence, e.g., an AASS target mRNA sequence, to direct the cleavage of the target RNA. In another embodiment, an RNAi agent of the invention is a dsRNA, each strand of which comprises 19-23 nucleotides, that interacts with a target RNA sequence, e.g., an AASS target mRNA sequence, to direct the cleavage of the target RNA. In one embodiment, the sense strand is 21 nucleotides in length. In another embodiment, the antisense strand is 23 nucleotides in length.

[0211] As used herein, the term “nucleotide overhang” refers to at least one unpaired nucleotide that protrudes from the duplex structure of an iRNA, e.g., a dsRNA. For example, when a 3'-end of one strand of a dsRNA extends beyond the 5'-end of the other strand, or vice versa, there is a nucleotide overhang. A dsRNA can comprise an overhang of at least one nucleotide; alternatively, the overhang can comprise at least two nucleotides, at least three nucleotides, at least four nucleotides, at least five nucleotides or more. A nucleotide overhang can comprise or consist of a nucleotide / nucleoside analog, including a deoxynucleotide / nucleoside. The overhang(s) can be on the sense strand, the antisense strand or any combination thereof. Furthermore, the nucleotide(s) of an overhang can be present on the 5'-end, 3'-end or both ends of either an antisense or sense strand of a dsRNA.

[0212] In one embodiment, the antisense strand of a dsRNA has a 1-10 nucleotide, e.g.. a 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotide, overhang at the 3'-end and / orthe 5'-end. In one embodiment, the sense strand ofa dsRNA has a 1-10 nucleotide, e.g.. a 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotide, overhang at the 3'-end and / orthe 5 '-end. In another embodiment, one or more of the nucleotides in the overhang is replaced with a nucleoside thiophosphate.

[0213] In certain embodiments, the overhang on the sense strand or the antisense strand, or both, can include extended lengths longer than 10 nucleotides, e.g., 10-30 nucleotides, 10-25 nucleotides, 10-20 nucleotides or 10-15 nucleotides in length. In certain embodiments, an extended overhang is on the sense strand of the duplex. In certain embodiments, an extended overhang is present on the 3 'end of the sense strand of the duplex. In certain embodiments, an extended overhang is present on the 5 'end of the sense strand of the duplex. In certain embodiments, an extended overhang is on the antisense strand of the duplex. In certain embodiments, an extended overhang is present on the 3 'end of the antisense strand of the duplex. In certain embodiments, an extended overhang is present on the 5 'end of tire antisense strand of the duplex. In certain embodiments, one or more of the nucleotides in the extended overhang is replaced with a nucleoside thiophosphate.

[0214] The terms “blunt” or “blunt ended” as used herein in reference to a dsRNA mean that there are no unpaired nucleotides or nucleotide analogs at a given terminal end of a dsRNA, i.e., no nucleotide overhang. One or both ends of a dsRNA can be blunt. Where both ends of a dsRNA are blunt, the dsRNA is said to be blunt ended. To be clear, a “blunt ended” dsRNA is a dsRNA that is blunt at both ends. i.e.. no nucleotide overhang at either end of the molecule. Most often such a molecule will be double-stranded over its entire length.

[0215] Tire term “antisense strand” or "guide strand" refers to the strand of an iRNA, e.g., a dsRNA, w hich includes a region that is substantially complementary to a target sequence, e.g., an AASS mRNA.

[0216] As used herein, the term “region of complementarity” refers to the region on the antisense strand that is substantially complementary to a sequence, for example a target sequence, e.g., an AASS nucleotide sequence, as defined herein. Where the region of complementarity is not fully complementary to the target sequence, the mismatches can be in the internal or terminal regions of the molecule. Generally, the most tolerated mismatches are in the terminal regions, e.g., within 5, 4, 3, or 2 nucleotides of the 5'- and / or 3'- terminus of the iRNA.

[0217] The term “sense strand” or "passenger strand" as used herein, refers to tire strand of an iRNA that includes a region that is substantially complementary to a region of the antisense strand as that tenn is defined herein.

[0218] As used herein, the term “cleavage region” refers to a region that is located immediately adjacent to the cleavage site. Tire cleavage site is the site on the target at which cleavage occurs. In some embodiments, the cleavage region comprises three bases on either end of, and immediately adjacent to, the cleavage site. In some embodiments, the cleavage region comprises two bases on either end of. and immediately adjacent to. the cleavage site. In some embodiments, the cleavage site specifically occurs at the site bound by nucleotides 10 and 11 of the antisense strand, and the cleavage region comprises nucleotides 11, 12 and 13.

[0219] As used herein, and unless otherwise indicated, the term "complementary ." when used to describe a first nucleotide sequence in relation to a second nucleotide sequence, refers to the ability of an oligonucleotide or polynucleotide comprising the first nucleotide sequence to hybridize and form a duplex structure under certain conditions with an oligonucleotide or polynucleotide comprising the second nucleotide sequence, as will be understood by the skilled person. Such conditions can, for example, be stringent conditions, where stringent conditions can include: 400 mM NaCl, 40 mM PIPES pH 6.4, 1 mM EDTA, 50°C or 70°C for 12-16 hours followed by washing (see, e.g., “Molecular Cloning: A Laboratory Manual, Sambrook, etal. (1989) Cold Spring Harbor Laboratory Press). Other conditions, such as physiologically relevant conditions as can be encountered inside an organism, can apply. The skilled person will be able to determine the set of conditions most appropriate for a test of complementarity of two sequences in accordance with the ultimate application of the hybridized nucleotides.

[0220] Complementary sequences within an iRNA, e.g., within a dsRNA as described herein, include basepairing of the oligonucleotide or polynucleotide comprising a first nucleotide sequence to an oligonucleotide or polynucleotide comprising a second nucleotide sequence over the entire length of one or both nucleotide sequences. Such sequences can be referred to as “fully complementary” with respect to each other herein. However, where a first sequence is referred to as “substantially complementary” with respect to a second sequence herein, the two sequences can be fully complementary, or they can form one or more, but generally not more than 5, 4, 3 or 2 mismatched base pairs upon hybridization for a duplex up to 30 base pairs, while retaining the ability to hybridize under tire conditions most relevant to their ultimate application, e.g., inhibition of gene expression via a RISC pathway. However, where two oligonucleotides are designed to form, upon hybridization, one or more single stranded overhangs, such overhangs shall not be regarded as mismatches with regard to the determination of complementarity. For example, a dsRNA comprising one oligonucleotide 21 nucleotides in length and another oligonucleotide 23 nucleotides in length, wherein the longer oligonucleotide comprises a sequence of 21 nucleotides that is fully complementary to the shorter oligonucleotide, can yet be referred to as “fully complementary” for the purposes described herein.

[0221] “Complementary” sequences, as used herein, can also include, or be formed entirely from, non- Watson-Crick base pairs and / or base pairs formed from non-natural and modified nucleotides, in so far as the above requirements with respect to their ability to hybridize are fulfilled. Such non-Watson-Crick base pairs include, but are not limited to, G:U Wobble or Hoogstein base pairing.

[0222] The terms “complementary,” “fully complementary " and “substantially complementary " herein can be used with respect to the base matching between the sense strand and the antisense strand of a dsRNA, or between the antisense strand of an iRNA agent and a target sequence, as will be understood from the context of their use.

[0223] As used herein, a polynucleotide that is “substantially complementary to at least part of' a messenger RNA (mRNA) refers to a polynucleotide that is substantially complementary to a contiguous portion of the mRNA of interest (e.g., an mRNA encoding AASS). For example, a polynucleotide is complementary to at least a part of an AASS mRNA if the sequence is substantially complementary' to a non-interrupted portion of an mRNA encoding AASS.

[0224] Accordingly, in some embodiments, the antisense strand polynucleotides disclosed herein are fully complementary to the target AASS sequence. In other embodiments, the antisense strand polynucleotides disclosed herein are substantially complementary to the target AASS sequence and comprise a contiguous nucleotide sequence which is at least about 80% complementary over its entire length to the equivalent region of the nucleotide sequence of SEQ ID NO: 1, or a fragment of SEQ ID NO: 1, such as about 85%, about 86%, about 87%, about 88%, about 89%, about 90%, about % 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% complementary.

[0225] In one embodiment, an RNAi agent of tire invention includes a sense strand that is substantially complementary to an antisense polynucleotide which, in turn, is complementary' to a target AASS sequence, and wherein the sense strand polynucleotide comprises a contiguous nucleotide sequence which is at least about 80% complementary' over its entire length to the equivalent region of the nucleotide sequence of SEQ ID NOs: 2, or a fragment of any one of SEQ ID NOs: 2, such as about 85%, about 86%, about 87%. about 88%, about 89%, about 90%, about % 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% complementary.

[0226] In some embodiments, an iRNA of the invention includes an antisense strand that is substantially complementary to the target AASS sequence and comprises a contiguous nucleotide sequence which is at least about 80% complementary over its entire length to the equivalent region of the nucleotide sequence of any one of the sense strands in Tables 3-6 or a fragment of any one of the sense strands in Tables 3-6, such as about 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% complementary, or 100% complementary.

[0227] Tire term “inhibiting,” as used herein, is used interchangeably with “reducing,” “silencing,” “downregulating,” “suppressing” and other similar terms, and includes any level of inhibition.

[0228] The phrase “inhibiting expression of an AASS gene,” as used herein, includes inhibition of expression of any AASS gene (such as. e.g., a mouse AASS gene, a rat AASS gene, a monkey AASS gene, or a human AASS gene) as well as variants or mutants of an AASS gene that encode an AASS protein.

[0229] “Inhibiting expression of an AASS gene” includes any level of inhibition of an AASS gene, e.g., at least partial suppression of the expression of an AASS gene, such as an inhibition by at least about 20%. In certain embodiments, inhibition is by at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%. at least about 60%, at least about 65%, at least about 70%. at least about 75%. at least about 80%. at least about 85%, at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99%.

[0230] Tire expression of an AASS gene may be assessed based on the level of any variable associated with AASS gene expression, e.g., AASS mRNA level or AASS protein level. The expression of an AASS gene may also be assessed indirectly based on, for example, a decrease in AASS protein activity, e.g., measuring a decrease in biological activity of AASS. e.g., a decrease in the production of saccharopine and / or 2- aminoadipic-4-semialdehyde; a decrease in the accumulation of glutaric acid and / or 3 -hydroxy-glutaric acid in a subject, and / or a decrease in alpha-aminoadipic semialdehyde (a-AASA) in urine and / or plasma. Inhibition may be assessed by a decrease in an absolute or relative level of one or more of these variables compared with a control level. The control level may be any type of control level that is utilized in the art, e.g.. a pre-dose baseline level, or a level determined from a similar subject, cell, or sample that is untreated or treated with a control (such as. e.g., buffer only control or inactive agent control).

[0231] In one embodiment, at least partial suppression of the expression of an AASS gene, is assessed by a reduction of the amount of AASS mRNA which can be isolated from, or detected, in a first cell or group of cells in w hich an AASS gene is transcribed and which has or have been treated such that the expression of an AASS gene is inhibited, as compared to a second cell or group of cells substantially identical to the first cell or group of cells but which has or have not been so treated (control cells). The degree of inhibition may be expressed in terms of:

[0232] (mRNA in control cells)

[0233] The phrase “contacting a cell with an RNAi agent,” such as a dsRNA. as used herein, includes contacting a cell by any possible means. Contacting a cell with an RNAi agent includes contacting a cell in vitro with the iRNA or contacting a cell in vivo with tire iRNA. The contacting may be done directly or indirectly. Thus, for example, the RNAi agent may be put into physical contact with the cell by the individual performing the method, or alternatively, the RNAi agent may be put into a situation that will permit or cause it to subsequently come into contact with the cell.

[0234] Contacting a cell in vitro may be done, for example, by incubating the cell with the RNAi agent. Contacting a cell in vivo may be done, for example, by injecting the RNAi agent into or near the tissue where the cell is located, or by injecting the RNAi agent into another area, e.g., the bloodstream or the subcutaneous space, such that the agent will subsequently reach the tissue where the cell to be contacted is located. For example, the RNAi agent may contain and / or be coupled to a ligand, e.g., GalNAc3, that directs the RNAi agent to a site of interest, e.g., the liver. Combinations of in vitro and in vivo methods of contacting are also possible. For example, a cell may also be contacted in vitro with an RNAi agent and subsequently transplanted into a subject.

[0235] In one embodiment, contacting a cell with an iRNA includes “introducing” or “delivering the iRNA into the cell” by facilitating or effecting uptake or absorption into the cell. Absorption or uptake of an iRNA can occur through unaided diffusive or active cellular processes, or by auxiliary agents or devices. Introducing an iRNA into a cell may be in vitro and / or in vivo. For example, for in vivo introduction, iRNA can be injected into a tissue site or administered systemically. In vivo delivery can also be done by a betaglucan delivery system, such as those described in U.S. Patent Nos. 5,032,401 and 5,607,677, and U.S. Publication No. 2005 / 0281781, the entire contents of which are hereby incorporated herein by reference. In vitro introduction into a cell includes methods known in the art such as electroporation and lipofection. Further approaches are described herein below and / or are known in the art.

[0236] The term “lipid nanoparticle” or “UNP” is a vesicle comprising a lipid layer encapsulating a pharmaceutically active molecule, such as a nucleic acid molecule, e.g., an iRNA or a plasmid from which an iRNA is transcribed. LNPs are described in, for example, U.S. Patent Nos. 6,858,225, 6,815,432, 8,158,601, and 8,058,069, the entire contents of which are hereby incorporated herein by reference.

[0237] As used herein, a “subject” is an animal, such as a mammal, including a primate (such as a human, a non-human primate, e.g., a monkey, and a chimpanzee), a non-primate (such as a cow, a pig, a camel, a llama, a horse, a goat, a rabbit, a sheep, a hamster, a guinea pig, a cat, a dog, a rat, a mouse, a horse, and a whale), or a bird (e.g., a duck or a goose). In an embodiment, the subject is a human, such as a human being treated or assessed for a disease, disorder or condition that would benefit from reduction in AASS expression; a human at risk for a disease, disorder or condition that would benefit from reduction in AASS expression; a human having a disease, disorder or condition that would benefit from reduction in AASS expression; and / or human being treated for a disease, disorder or condition that would benefit from reduction in AASS expression as described herein.

[0238] As used herein, the terms “treating” or “treatment” refer to a beneficial or desired result including, but not limited to, alleviation or amelioration of one or more symptoms associated with AASS gene expression and / or AASS protein production, e.g., an AASS-associated disease, such as a lysine catabolism disorder. In one embodiment, the lysine catabolism disorder is glutaric aciduria type 1 (GAI) or pyridoxine-dependent epilepsy (PDE). "Treatment" can also mean prolonging survival as compared to expected survival in the absence of treatment.

[0239] The term “lower” in the context of an AASS-associated disease refers to a statistically significant decrease in such level. The decrease can be, for example, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or more. In certain embodiments, a decrease is at least 20%. “Lower” in the context of the level of AASS in a subject is preferably down to a level accepted as within the range of nonnal for an individual without such disorder.

[0240] As used herein, “prevention” or “preventing,” when used in reference to a disease, disorder or condition thereof, that would benefit from a reduction in expression of an AASS gene, refers to a reduction in the likelihood that a subject will develop a symptom associated with such disease, disorder, or condition, e.g., a symptom of AASS gene expression, such as encephalopathic crisis, bilateral striatal brain injury, complex movement disorders, accumulation of Glutaryl-CoA byproducts, e.g., glutaric acid (GA) and 3-hydroxy glutaric acid (3-OH-GA), seizures, neurologic abnormalities, an increased concentration of alpha-aminoadipic semialdehyde (a-AASA) or pipecolic acid in urine and / or plasma, and intellectual disability. The failure to develop a disease, disorder or condition, or the reduction in the development of a symptom associated with such a disease, disorder or condition (e.g., by at least about 10% on a clinically accepted scale forthat disease or disorder), or the exhibition of delayed symptoms (e.g., reduction in encephalopathic crisis, bilateral striatal brain injury, complex movement disorders, accumulation of Glutaryl-CoA byproducts, e.g., glutaric acid (GA) and 3-hydroxy glutaric acid (3-OH-GA), seizures, neurologic abnonnalities. the concentration of alphaaminoadipic semialdehyde (a-AASA) in urine and / or plasma, and intellectual disability) delayed (e.g., by days, weeks, months or years) is considered effective prevention.

[0241] As used herein, the term "AASS-associated disease,” is a disease or disorder that is caused by, or associated with, AASS gene expression or AASS protein production. The term "AASS-associated disease” includes a disease, disorder or condition that would benefit from a decrease in AASS gene expression or protein activity. In one embodiment, an "AASS-associated disease” is a lysine catabolism disorder. A “lysine catabolism disorder” is any disease, disorder, or condition associated with the lysine catabolism pathway. Non-limiting examples of lysine catabolism disorders include, for example, glutaric aciduria type 1 (GAI) and pyridoxine -dependent epilepsy (PDE).

[0242] "Therapeutically effective amount," as used herein, is intended to include the amount of an RNAi agent that, when administered to a subject having an AASS-associated disease, disorder, or condition, is sufficient to effective treatment of the disease (e.g., by diminishing, ameliorating or maintaining the existing disease or one or more symptoms of disease). The "therapeutically effective amount" may vary depending on the RNAi agent, how the agent is administered, the disease and its severity and the history, age, weight, family history, genetic makeup, the types of preceding or concomitant treatments, if any, and other individual characteristics of the subject to be treated.

[0243] “Prophylactically effective amount,” as used herein, is intended to include the amount of an iRNA that, when administered to a subject having an AASS-associated disease, disorder, or condition, is sufficient to prevent or ameliorate the disease or one or more symptoms of the disease. Ameliorating the disease includes slowing the course of the disease or reducing the severity of later-developing disease. The "prophylactically effective amount" may vary depending on the iRNA, how the agent is administered, the degree of risk of disease, and the history, age, weight, family history, genetic makeup, the types of preceding or concomitant treatments, if any. and other individual characteristics of tire patient to be treated.

[0244] A "therapeutically-effective amount" or “prophylactically effective amount” also includes an amount of an RNAi agent that produces some desired local or systemic effect at a reasonable benefit / risk ratio applicable to any treatment. iRNA employed in tire methods of the present invention may be administered in a sufficient amount to produce a reasonable benefit / risk ratio applicable to such treatment.

[0245] The phrase "pharmaceutically acceptable" is employed herein to refer to those compounds, materials, compositions, and / or dosage fonns which are. within the scope of sound medical judgment, suitable for use in contact with the tissues of human subjects and animal subjects without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit / risk ratio.

[0246] Tire phrase "pharmaceutically -acceptable carrier" as used herein means a pharmaceutically-acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, manufacturing aid (e.g., lubricant, talc magnesium, calcium or zinc stearate, or steric acid), or solvent encapsulating material, involved in carrying or transporting the subject compound from one organ, or portion of the body, to another organ, or portion of the body. Each carrier must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not injurious to the subject being treated. Some examples of materials which can serve as phannaccutically-acccptablc carriers include: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as com starch and potato starch; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) lubricating agents, such as magnesium stearate, sodium lauryl sulfate and talc: (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, com oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide: (15) alginic acid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer's solution; (19) ethyl alcohol; (20) pH buffered solutions: (21) polyesters, polycarbonates and / or polyanhydrides: (22) bulking agents, such as polypeptides and amino acids (23) serum component, such as serum albumin, HDL and LDL; and (22) other non-toxic compatible substances employed in pharmaceutical formulations.

[0247] Tire term “sample,” as used herein, includes a collection of similar fluids, cells, or tissues isolated from a subject, as well as fluids, cells, or tissues present within a subject. Examples of biological fluids include blood, serum and serosal fluids, plasma, cerebrospinal fluid, ocular fluids, lymph, urine, saliva, and the like. Tissue samples may include samples from tissues, organs or localized regions. For example, samples may be derived from particular organs, parts of organs, or fluids or cells within those organs. In certain embodiments, samples may be derived from tire liver (e.g., whole liver or certain segments of liver or certain types of cells in the liver, such as, e.g., hepatocytes). In some embodiments, a “sample derived from a subject” refers to blood or plasma drawn from the subject.

[0248] IL iRNAs of the Invention

[0249] Described herein are iRNAs which inhibit the expression of a target gene. In one embodiment, the iRNAs inhibit the expression of an AASS gene. In one embodiment, the iRNA agent includes double stranded ribonucleic acid (dsRNA) molecules for inhibiting the expression of an AASS gene in a cell, such as a liver cell, such as a liver cell within a subject, e.g., a mammal, such as a human having a lysine catabolism disease, disorder, or condition.

[0250] The dsRNA includes an antisense strand having a region of complementarity which is complementary to at least a part of an mRNA formed in the expression of an AASS gene. Tire region of complementarity is about 30 nucleotides or less in length (e.g., about 30, 29, 28, 27, 26, 25, 24, 23, 22, 21, 20, 19, or 18 nucleotides or less in length). Upon contact with a cell expressing the target gene, the iRNA inhibits the expression of the target gene (e.g., a human, a primate, a non-primate, or a rodent target gene) by at least about 10% as assayed by, for example, a PCR or branched DNA (bDNA)-based method, or by a protein -based method, such as by immunofluorescence analysis, using, for example. Western Blotting or flowcytometric techniques.

[0251] A dsRNA includes two RNA strands that are complementary and hybridize to form a duplex structure under conditions in which the dsRNA will be used. One strand of a dsRNA (the antisense strand) includes a region of complementarity that is substantially complementary, and generally fully complementary, to a target sequence. The target sequence can be derived from the sequence of an mRNA formed during the expression of an AASS gene. The other strand (the sense strand) includes a region that is complementary to the antisense strand, such that tire two strands hybridize and form a duplex structure when combined under suitable conditions. As described elsewhere herein and as known in the art, the complementary sequences of a dsRNA can also be contained as self-complementary regions of a single nucleic acid molecule, as opposed to being on separate oligonucleotides.

[0252] Generally, the duplex structure is between 15 and 30 base pairs in length, e.g., between, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-

[0253] 26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30. 20-29, 20-28, 20-27, 20-26, 20-25, 20-24,20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-

[0254] 27, 21-26, 21-25, 21-24. 21-23, or 21-22 base pairs in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the invention.

[0255] Similarly, the region of complementarity to the target sequence is between 15 and 30 nucleotides in length, e.g., between 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15- 17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27,

[0256] 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28. 20-27, 20-26, 20-25, 20-24,20-23, 20- 22, 20-21, 21-30, 21-29. 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 nucleotides in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the invention.

[0257] In some embodiments, the sense and antisense strands of the dsRNA are each independently about 15 to about 30 nucleotides in length, or about 25 to about 30 nucleotides in length, e.g., each strand is independently between 15-29, 15-28, 15-27. 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17. 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24. 18-23, 18-22. 18-21, 18-20, 19-30, 19-29, 19-28, 19- 27, 19-26. 19-25, 19-24. 19-23, 19-22. 19-21. 19-20, 20-30. 20-29, 20-28. 20-27, 20-26. 20-25, 20-24,20-23,

[0258] 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 nucleotides in length. In some embodiments, the dsRNA is between about 15 and about 23 nucleotides in length, or between about 25 and about 30 nucleotides in length. In general, the dsRNA is long enough to serve as a substrate for the Dicer enzyme. For example, it is well known in the art that dsRNAs longer than about 21-23 nucleotides can serve as substrates for Dicer. As tire ordinarily skilled person will also recognize, the region of an RNA targeted for cleavage will most often be part of a larger RNA molecule, often an mRNA molecule. Where relevant, a “part” of an mRNA target is a contiguous sequence of an mRNA target of sufficient length to allow it to be a substrate for RNAi-directed cleavage (i.e., cleavage through a RISC pathway).

[0259] One of skill in the art will also recognize that the duplex region is a primary functional portion of a dsRNA, e.g., a duplex region of about 9 to 36 base pairs, e.g., about 10-36, 11-36, 12-36, 13-36, 14-36, 15-36, 9-35, 10-35. 11-35, 12-35. 13-35, 14-35, 15-35, 9-34, 10-34, 11-34, 12-34, 13-34. 14-34, 15-34. 9-33. 10-33, 11-33, 12-33, 13-33, 14-33, 15-33, 9-32, 10-32, 11-32, 12-32, 13-32, 14-32, 15-32, 9-31, 10-31, 11-31, 12-31, 13-32, 14-31, 15-31, 15-30, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15- 18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24,20- 23, 20-22, 20-21, 21-30. 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 base pairs. Thus, in one embodiment, to the extent that it becomes processed to a functional duplex, of e.g., 15-30 base pairs, that targets a desired RNA for cleavage, an RNA molecule or complex of RNA molecules having a duplex region greater than 30 base pairs is a dsRNA. Thus, an ordinarily skilled artisan will recognize that in one embodiment, a MicroRNA (miRNA) is a dsRNA. In another embodiment, a dsRNA is not a naturally occurring miRNA. In another embodiment, an iRNA agent useful to target AASS expression is not generated in the target cell by cleavage of a larger dsRNA.

[0260] A dsRNA as described herein can further include one or more single-stranded nucleotide overhangs e.g., 1, 2, 3, or 4 nucleotides. dsRNAs having at least one nucleotide overhang can have unexpectedly superior inhibitory’ properties relative to their blunt-ended counterparts. A nucleotide overhang can comprise or consist of a nucleotide / nucleoside analog, including a deoxynucleotide / nucleoside. The overhang(s) can be on the sense strand, the antisense strand or any combination thereof. Furthennore, the nucleotide(s) of an overhang can be present on the 5'-end. 3'-end or both ends of either an antisense or sense strand of a dsRNA.

[0261] A dsRNA can be synthesized by standard methods known in the art as further discussed below, e.g., by use of an automated DNA synthesizer, such as are commercially available from, for example. Biosearch, Applied Biosystems, Inc. iRNA compounds of the invention may be prepared using a two-step procedure. First, the individual strands of the double-stranded RNA molecule are prepared separately. Then, the component strands are annealed. The individual strands of the siRNA compound can be prepared using solution-phase or solid-phase organic synthesis or both. Organic synthesis offers the advantage that the oligonucleotide strands comprising unnatural or modified nucleotides can be easily prepared. Single-stranded oligonucleotides of the invention can be prepared using solution-phase or solid-phase organic synthesis or both.

[0262] In one aspect, a dsRNA of the invention includes at least two nucleotide sequences, a sense sequence and an antisense sequence. The sense strand sequence is selected from tire group of sequences provided in Tables 3-6, and the corresponding nucleotide sequence of the antisense strand of tire sense strand is selected from the group of sequences of Tables 3-6. In this aspect, one of the two sequences is complementary to the other of the two sequences, with one of the sequences being substantially complementary to a sequence of an mRNA generated in the expression of an AASS gene. As such, in this aspect, a dsRNA will include two oligonucleotides, where one oligonucleotide is described as the sense strand (passenger strand) in Tables 3-6, and the second oligonucleotide is described as the corresponding antisense strand (guide strand) of the sense strand in Tables 3-6. In one embodiment, the substantially complementary sequences of tire dsRNA are contained on separate oligonucleotides. In another embodiment, the substantially complementary sequences of the dsRNA are contained on a single oligonucleotide.

[0263] It will be understood that, although the sequences in Tables 3-6 are described as modified, unmodified, unconjugated, and / or conjugated sequences, the RNA of the iRNA of the invention e.g., a dsRNA of the invention, may comprise any one of the sequences set forth Tables 3-6 that is un-modified, unconjugated, and / or modified and / or conjugated differently than described therein.

[0264] The skilled person is well aware that dsRNAs having a duplex structure of between about 20 and 23 base pairs, e.g., 21, base pairs have been hailed as particularly effective in inducing RNA interference (Elbashir et al., (2001) EMBO J., 20:6877-6888). However, others have found that shorter or longer RNA duplex structures can also be effective (Chu and Rana (2007) RNA 14:1714-1719; Kim et al. (2005) Nat Biotech 23:222-226). In the embodiments described above, by virtue of the nature of the oligonucleotide sequences provided herein, dsRNAs described herein can include at least one strand of a length of minimally 21 nucleotides. It can be reasonably expected that shorter duplexes minus only a few nucleotides on one or both ends can be similarly effective as compared to the dsRNAs described above. Hence, dsRNAs having a sequence of at least 15, 16, 17, 18, 19, 20, or more contiguous nucleotides derived from one of the sequences provided herein, and differing in their ability to inhibit the expression of an AASS gene by not more than about 5, 10, 15, 20, 25, or 30 % inhibition from a dsRNA comprising the full sequence, are contemplated to be within the scope of the present invention.

[0265] In addition, the RNAs described in Tables 3-6 identify a site(s) in an AASS transcript that is susceptible to RISC-mediated cleavage. As such, the present invention further features iRNAs that target within this site(s). As used herein, an iRNA is said to target within a particular site of an RNA transcript if the iRNA promotes cleavage of the transcript anywhere within that particular site. Such an iRNA will generally include at least about 15 contiguous nucleotides from one of the sequences provided herein coupled to additional nucleotide sequences taken from the region contiguous to the selected sequence in the gene.

[0266] While a target sequence is generally about 15-30 nucleotides in length, there is wide variation in the suitability of particular sequences in this range for directing cleavage of any given target RNA. Various software packages and tire guidelines set out herein provide guidance for the identification of optimal target sequences for any given gene target, but an empirical approach can also be taken in which a “window” or “mask” of a given size (as a non-limiting example, 21 nucleotides) is literally or figuratively (including, e.g., in silico) placed on the target RNA sequence to identify sequences in the size range that can serve as target sequences. By moving the sequence “window” progressively one nucleotide upstream or downstream of an initial target sequence location, the next potential target sequence can be identified, until the complete set of possible sequences is identified for any given target size selected. This process, coupled with systematic synthesis and testing of the identified sequences (using assays as described herein or as known in the art) to identify those sequences that perform optimally can identify those RNA sequences that, when targeted with an iRNA agent, mediate the best inhibition of target gene expression. Thus, while the sequences identified herein represent effective target sequences, it is contemplated that further optimization of inhibition efficiency can be achieved by progressively “walking the window” one nucleotide upstream or downstream of the given sequences to identify sequences with equal or better inhibition characteristics.

[0267] Further, it is contemplated that for any sequence identified herein, further optimization could be achieved by systematically either adding or removing nucleotides to generate longer or shorter sequences and testing those sequences generated by walking a window of the longer or shorter size up or down the target RNA from that point. Again, coupling this approach to generating new candidate targets with testing for effectiveness of iRNAs based on those target sequences in an inhibition assay as known in the art and / or as described herein can lead to further improvements in the efficiency of inhibition. Further still, such optimized sequences can be adjusted by, e.g., the introduction of modified nucleotides as described herein or as known in the art, addition or changes in overhang, or other modifications as known in the art and / or discussed herein to further optimize the molecule (e.g., increasing serum stability or circulating half-life, increasing thermal stability, enhancing transmembrane deli very, targeting to a particular location or cell type, increasing interaction with silencing pathway enzymes, increasing release from endosomes) as an expression inhibitor.

[0268] An iRNA agent as described herein can contain one or more mismatches to the target sequence. In one embodiment, an iRNA as described herein contains no more than 3 mismatches. If the antisense strand of the iRNA contains mismatches to a target sequence, it is preferable that the area of mismatch is not located in the center of the region of complementarity. If the antisense strand of the iRNA contains mismatches to the target sequence, it is preferable that the mismatch be restricted to be within the last 5 nucleotides from either the 5'- or 3 '-end of the region of complementarity. For example, for a 23 nucleotide iRNA agent the strand which is complementary to a region of an AASS gene, generally does not contain any mismatch within the central 13 nucleotides. The methods described herein or methods known in the art can be used to determine whether an iRNA containing a mismatch to a target sequence is effective in inhibiting the expression of an AASS gene. Consideration of the efficacy of iRNAs with mismatches in inhibiting expression of an AASS gene is important, especially if the particular region of complementarity in an AASS gene is known to have polymorphic sequence variation within the population.

[0269] An RNA target may have regions, or spans of the target RNA's nucleotide sequence, which are relatively more susceptible or amenable than other regions of the RNA target to mediating cleavage of the RNA target via RNA interference induced by the binding of an RNAi agent to that region. The increased susceptibility to RNA interference within such “hotspot regions” (or simply “hotspots”) means that iRNA agents targeting the region will likely have higher efficacy in inducing iRNA interference than iRNA agents which target other regions of the target RNA. For example, without being bound by theory, tire accessibility of a target region of a target RNA may influence the efficacy of iRNA agents which target that region, with some hotspot regions having increased accessibility. Secondary structures, for instance, that form in the RNA target (e.g., within or proximate to hotspot regions) may affect the ability of the iRNA agent to bind the target region and induce RNA interference.

[0270] According to certain aspects of the invention, an iRNA agent may be designed to target a hotspot region of any of the target RNAs described herein, including any identified portions of a target RNA (e.g., a particular exon). As used herein, a hotspot region may refer to an approximately 19-200, 19-150, 19-100. 19- 75, 19-50. 21-200. 21-150, 21-100, 21-75. 21-50, 50-200, 50-150. 50-100, 50-75, 75-200. 75-150, 75-100, 100-200, or 100-150 nucleotide region of a target RNA sequence for which targeting using RNAi agents provides an observably higher probability of efficacious silencing relative to targeting other regions of the same target RNA. According to certain aspects of the invention, a hotspot region may comprise a limited region of the target RNA, and in some cases, a substantially limited region of the target, including for example, less than half of the length of tire target RNA, such as about 5%. 10%. 15%, 20%, 25%, or 30% of the length of the target RNA. Conversely, the other regions against which a hotspot is compared may cumulatively comprise at least a majority of the length of the target RNA. For example, the other regions may cumulatively comprise at least about 60%, or at least about 70%, or at least about 80%, or at least about 90%, or at least about 95% of the length of the target RNA.

[0271] Compared regions of the target RNA may be empirically evaluated for identification of hotspots using efficacy data obtained from in vitro or in vivo screening assays. For example, RNAi agents targeting various regions that span a target RNA may be compared for frequency of efficacious iRNA agents (e.g., the amount by which target gene expression is inhibited, such as measured by mRNA expression or protein expression) that bind each region. In general, a hotspot can be recognized by observing clustering of multiple efficacious RNAi agents that bind to a limited region of the RNA target. A hotspot may be sufficiently characterized as such by observing efficacy of iRNA agents which cumulatively span at least about 60% of the target region identified as a hotspot, such as about 70%, about 80%, about 90%, or about 95% or more of the length of the region, including both ends of the region (i.e. at least about 60%, 70%, 80%, 90%, or 95% or more of the nucleotides within the region, including the nucleotides at each end of the region, were targeted by an iRNA agent). According to some aspects of the invention, an iRNA agent which demonstrates at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% inhibition over the region (e.g., no more than about 50%, 45%, 40%, 35%, 30%. 25%, 20%, 15%, 10%, or 5% mRNA remaining) may be identified as efficacious.

[0272] Amenability to targeting of RNA regions may also be assessed using quantitative comparison of inhibition measurements across different regions of a defined size (e.g, 25, 30, 40, 50, 60, 70, 80, 90, or 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, or 200 nts). For example, an average level of inhibition may be determined for each region and the averages of each region may be compared. Tire average level of inhibition within a hotspot region may be substantially higher than the average of averages for all evaluated regions. According to some aspects, the average level of inhibition in a hotspot region may be at least about 10%, 20%, 30%, 40%, or 50% higher than the average of averages. According to some aspects, the average level of inhibition in a hotspot region may be at least about 1.0, 1.1, 1.2, 1.3, 1.4, 1.5 1.6, 1.7, 1.8. 1.9, or 2.0 standard deviations above the average of averages. The average level of inhibition may be higher by a statistically significant (e.g., p < 0.05) amount. According to some aspects, each inhibition measurement within a hotspot region may be above a threshold amount (e.g.. at or below a threshold amount of mRNA remaining). According to some aspects, each inhibition measurement within the region may be substantially higher than an average of all inhibition measurements across all the measured regions. For example, each inhibition measurement in a hotspot region may be at least about 10%, 20%, 30%, 40%, or 50% higher than the average of all inhibition measurements. According to some aspects, each inhibition measurement may be at least about 1.0, 1.1, 1.2, 1.3, 1.4, 1.5 1.6, 1.7, 1.8. 1.9, or 2.0 standard deviations above the average of all inhibition measurements. Each inhibition measurement may be higher by a statistically significant (e.g., p < 0.05) amount than the average of all inhibition measurements. A standard for evaluating a hotspot may comprise various combinations of the above standards where compatible (e.g., an average level of inhibition of at least about a first amount and having no inhibition measurements below a threshold level of a second amount, lesser than the first amount).

[0273] It is therefore expressly contemplated that any iRNA agent, including the specific exemplary iRNA agents described herein, which targets a hotspot region of a target RNA. may be preferably selected for inducing RNA interference of the target mRNA as targeting such a hotspot region is likely to exhibit a robust inhibitory response relative to targeting a region which is not a hotspot region. RNAi agents targeting target sequences that substantially overlap (e.g., by at least about 70%, 75%, 80%, 85%, 90%, 95% of the target sequence length) or, preferably, that reside fully within the hotspot region may be considered to target the hotspot region. Hotspot regions of the RNA target(s) of the instant invention may include any region for which the data disclosed herein demonstrates higher frequency of targeting by efficacious RNAi agents, including by any of the standards described elsewhere herein, whether or not the range(s) of such hotspot region(s) are explicitly specified.

[0274] In various embodiments, a dsRNA agent of the present invention targets a hotspot region of an mRNA encoding AASS.

[0275] III. Modified iRNAs of the Invention

[0276] In one embodiment, the RNA of the iRNA of the invention e.g.. a dsRNA, is un-modified, and does not comprise, e.g.. chemical modifications and / or conjugations known in the art and described herein. In another embodiment, the RNA of an iRNA of the invention, e.g., a dsRNA, is chemically modified to enhance stability or other beneficial characteristics. In certain embodiments of the invention, substantially all of the nucleotides of an iRNA of the invention arc modified. In other embodiments of the invention, all of the nucleotides of an iRNA of the invention are modified. iRNAs of the invention in which “substantially all of the nucleotides are modified” are largely but not wholly modified and can include not more than 5, 4, 3, 2, or 1 unmodified nucleotides.

[0277] In some aspects of the invention, substantially all of tire nucleotides of an iRNA of the invention are modified and the iRNA agents comprise no more than 10 nucleotides comprising 2'-fluoro modifications (e.g., no more than 9 2'-fluoro modifications, no more than 8 2'-fluoro modifications, no more than 7 2'-fluoro modifications, no more than 6 2'-fluoro modifications, no more than 5 2'-fluoro modifications, no more than 4 2'-fluoro modifications, no more than 5 2'-fluoro modifications, no more than 4 2'-fluoro modifications, no more than 3 2'-fluoro modifications, or no more than 2 2'-fluoro modifications). For example, in some embodiments, the sense strand comprises no more than 4 nucleotides comprising 2'-fluoro modifications (e.g.. no more than 3 2'-fluoro modifications, or no more than 2 2'-fluoro modifications). In other embodiments, the antisense strand comprises no more than 6 nucleotides comprising 2'-fluoro modifications (e.g., no more than 5 2'-fluoro modifications, no more than 4 2'-fluoro modifications, no more than 4 2'-fluoro modifications, or no more than 2 2'-fluoro modifications).

[0278] In other aspects of the invention, all of the nucleotides of an iRNA of the invention are modified and the iRNA agents comprise no more than 10 nucleotides comprising 2 ‘-fluoro modifications (e.g., no more than 9 2'-fluoro modifications, no more than 8 2'-fluoro modifications, no more than 7 2'-fluoro modifications, no more than 6 2'-fluoro modifications, no more than 5 2'-fluoro modifications, no more than 4 2'-fluoro modifications, no more than 5 2'-fluoro modifications, no more than 4 2'-fluoro modifications, no more than 3 2'-fluoro modifications, or no more than 2 2'-fluoro modifications).

[0279] In one embodiment, the double stranded RNAi agent of the invention further comprises a 5'- phosphate or a 5'-phosphate mimic at the 5' nucleotide of the antisense strand. In another embodiment, the double stranded RNAi agent further comprises a 5'-phosphate mimic at the 5' nucleotide of the antisense strand. In a specific embodiment, the 5‘-phosphate mimic is a 5'-vinyl phosphonate (5 -VP). In one embodiment, the phosphate mimic is a 5 ‘-cyclopropyl phosphonate. In some embodiments, the 5 '-end of the antisense strand of the double-stranded iRNA agent does not contain a 5'-vinyl phosphonate (VP).

[0280] In one embodiment, at least one of the modified nucleotides is selected from the group consisting of a deoxy-nucleotide, a 2'-O-methyl modified nucleotide, a 2'-fluoro modified nucleotide, a 2'-deoxy- modified nucleotide, a glycol modified nucleotide (GNA), e.g., Ggn, Cgn, Tgn. or Agn, a nucleotide with a 2' phosphate, e.g., G2p, C2p, A2p or U2p, and, a vinyl-phosphonate nucleotide; and combinations thereof. In other embodiments, each of the duplexes of Tables 4 or 6 may be particularly modified to provide another double-stranded iRNA agent of the present disclosure. In one example, the 3'-terminus of each sense duplex may be modified by removing the 3 '-terminal L96 ligand and exchanging the two phosphodiester intemucleotide linkages between the three 3 '-terminal nucleotides with phosphorothioate intemucleotide linkages. That is, the three 3 '-terminal nucleotides (N) of a sense sequence of tire formula: may be replaced with while the antisense sequence remains unchanged to provide another double-stranded iRNA agent of the present disclosure.

[0281] The nucleic acids featured in the invention can be synthesized and / or modified by methods well established in the art, such as those described in “Current protocols in nucleic acid chemistry,” Beaucage, S.L. et al. (Edrs.), John Wiley & Sons, Inc., New York, NY, USA, which is hereby incorporated herein byreference. Modifications include, for example, end modifications, e.g., 5 '-end modifications (phosphorylation, conjugation, inverted linkages) or 3 '-end modifications (conjugation, DNA nucleotides, inverted linkages, efc.); base modifications, e.g., replacement with stabilizing bases, destabilizing bases, or bases that base pair with an expanded repertoire of partners, removal of bases (abasic nucleotides), or conjugated bases; sugar modifications (e.g. , at the 2'-position or 4'-position) or replacement of the sugar; and / or backbone modifications, including modification or replacement of the phosphodiester linkages. Specific examples of iRNA compounds useful in the embodiments described herein include, but are not limited to RNAs containing modified backbones or no natural intemucleoside linkages. RNAs having modified backbones include, among others, those that do not have a phosphorus atom in the backbone. For the purposes of this specification, and as sometimes referenced in the art, modified RNAs that do not have a phosphorus atom in their intemucleoside backbone can also be considered to be oligonucleosides. In some embodiments, a modified iRNA will have a phosphorus atom in its intemucleoside backbone.

[0282] Modified RNA backbones include, for example, phosphorothioates, chiral phosphorothioates. phosphorodithioates, phosphotriesters, aminoalkylphosphotriesters, methyl and other alkyl phosphonates including 3'-alkylene phosphonates and chiral phosphonates, phosphinates, phosphoramidates including 3'-amino phosphoramidate and aminoalkylphosphoramidates, thionophosphoramidates, thionoalkylphosphonates, thionoalkylphosphotriesters, and boranophosphates having normal 3'-5* linkages, 2'-5'-linked analogs of these, and those having inverted polarity wherein the adjacent pairs of nucleoside units are linked 3'-5' to 5'-3' or 2 -5' to 5'-2'. Various salts, mixed salts and free acid forms are also included. In some embodiments of the invention, the dsRNA agents of the invention are in a free acid form. In other embodiments of the invention, the dsRNA agents of the invention are in a salt form. In one embodiment, the dsRNA agents of the invention are in a sodium salt form. In certain embodiments, when the dsRNA agents of the invention are in the sodium salt form, sodium ions are present in the agent as counterions for substantially all of the phosphodiester and / or phosphorothiotate groups present in the agent. Agents in which substantially all of tire phosphodiester and / or phosphorothioate linkages have a sodium counterion include not more than 5, 4, 3, 2, or 1 phosphodiester and / or phosphorothioate linkages without a sodium counterion. In some embodiments, when the dsRNA agents of the invention are in the sodium salt fonn. sodium ions are present in the agent as counterions for all of the phosphodiester and / or phosphorothiotate groups present in the agent.

[0283] Representative U.S. patents that teach the preparation of the above phosphorus-containing linkages include, but are not limited to, U.S. Patent Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243; 5,177,195; 5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717; 5,321,131; 5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677; 5,476,925; 5,519,126; 5,536,821; 5,541,316; 5,550,111; 5,563,253; 5,571,799; 5,587,361; 5,625,050; 6.028,188; 6,124.445; 6,160,109; 6,169,170; 6,172.209; 6, 239.265; 6,277,603; 6,326.199; 6,346,614; 6.444,423; 6,531.590; 6,534,639; 6,608,035; 6.683.167; 6,858,715; 6,867,294; 6,878,805; 7,015,315; 7,041,816; 7,273,933; 7,321,029; and US Pat RE39464, the entire contents of each of which are hereby incorporated herein by reference.

[0284] Modified RNA backbones that do not include a phosphorus atom therein have backbones that are fonned by short chain alkyl or cycloalkyl intemucleoside linkages, mixed heteroatoms and alkyl or cycloalkyl intemucleoside linkages, or one or more short chain heteroatomic or heterocyclic intemucleoside linkages. These include those having morpholino linkages (formed in part from the sugar portion of a nucleoside); siloxane backbones; sulfide, sulfoxide and sulfone backbones; formacetyl and thioformacetyl backbones; methylene formacetyl and thioformacetyl backbones; alkene containing backbones; sulfamate backbones; methyleneimino and methylenehydrazino backbones; sulfonate and sulfonamide backbones; amide backbones; and others having mixed N, O, S and CH2component parts.

[0285] Representative U.S. patents that teach the preparation of tire above oligonucleosides include, but are not limited to. U.S. Patent Nos. 5.034.506; 5,166,315; 5,185,444; 5.214.134; 5,216,141; 5,235,033; 5.64,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967; 5,489,677; 5,541,307; 5,561,225; 5,596,086;

[0286] 5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312; 5,633,360; 5,677,437; and, 5,677,439, the entire contents of each of which are hereby incorporated herein by reference.

[0287] In other embodiments, suitable RNA mimetics are contemplated for use in iRNAs, in which both the sugar and the intemucleoside linkage, i.e.. the backbone, of the nucleotide units are replaced with novel groups. Tire base units are maintained for hybridization with an appropriate nucleic acid target compound. One such oligomeric compound, an RNA mimetic that has been shown to have excellent hybridization properties, is referred to as a peptide nucleic acid (PNA). In PNA compounds, the sugar backbone of an RNA is replaced with an amide containing backbone, in particular an aminocthylglycinc backbone. The nucleobases are retained and are bound directly or indirectly to aza nitrogen atoms of the amide portion of tire backbone. Representative U.S. patents that teach the preparation of PNA compounds include, but are not limited to, U.S. Patent Nos. 5,539,082; 5,714,331; and 5,719,262, the entire contents of each of which are hereby incorporated herein by reference. Additional PNA compounds suitable for use in the iRNAs of the invention are described in, for example, in Nielsen et al., Science, 1991, 254, 1497-1500.

[0288] Some embodiments featured in the invention include RNAs with phosphorothioate backbones and oligonucleosides with heteroatom backbones, and in particular -CH2-NH— CH2-, — CH2— N(CH3)“O-CH2- [known as a methylene (methylimino) or MMI backbone), — CH2— 0— N(CH3)--CH2--, — CH2-N(CH3)— N(CH3)-CH2- and — N(CH3)-CH2-CH2— [wherein the native phosphodiester backbone is represented as — O- -P— O--CH2--] of the above-referenced U.S. Patent No. 5,489,677, and the amide backbones of the abovereferenced U.S. Patent No. 5,602,240. In some embodiments, the RNAs featured herein have morpholino backbone structures of the above-referenced U.S. Patent No. 5,034,506.

[0289] Modified RNAs can also contain one or more substituted sugar moieties. The iRNAs, e.g., dsRNAs, featured herein can include one of the following at the 2'-position: OH; F; O-, S-, or N-alkyl; O-, S-, or N- alkenyl; O-, S- or N-alkynyl; or O-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynyl can be substituted or unsubstituted C1to C10alkyl or C2 to C10alkenyl and alkynyl. Exemplary suitable modifications include O[(CH2)„O]mCH3, O(CH2).nOCH3, O(CH2)nNH2, O(CH2)nCH3, O(CH2)nONH2, and O(CH2)nON[(CH2)nCH3)]2, where n and m are from 1 to about 10. In other embodiments, dsRNAs include one of the following at the 2' position; Ci to C10lower alkyl, substituted lower alkyl, alkaryl, aralkyl, O-alkaryl or O-aralkyl, SH, SCH3. OCN, Cl, Br. CN, CF3. OCF3, SOCH3, SO2CH3, ONO2, NO2. N3. NH2. heterocycloalkyl, heterocycloalkaryl, aminoalkylamino, polyalkylamino, substituted silyl, an RNA cleaving group, a reporter group, an intercalator, a group for improving tire pharmacokinetic properties of an iRNA, or a group for improving the pharmacodynamic properties of an iRNA, and other substituents having similar properties. In some embodiments, the modification includes a 2'-methoxyethoxy (2 -O— CH2CH2OCH3, also known as 2'-O-(2-methoxyethyl) or 2'-M0E) (Martin et al., Helv. Chim. Acta. 1995, 78:486-504) i.e., an alkoxy-alkoxy group. Another exemplary modification is 2'-dimethylaminooxyethoxy, i.e., a O(CH2)2ON(CH3)2group, also known as 2'-DMAOE, as described in examples herein below, and 2'- dimethylaminoethoxyethoxy (also known in the art as 2,-O-dimethylaminoethoxyethyl or 2'-DMAEOE), i.e., 2'-O— CH2— O— CH2— N(CH2)2. Further exemplary modifications include: 5'-Me-2'-F nucleotides, 5'-Me-2'- OMe nucleotides, 5'-Me-2'-deoxynucleotides, (both R and S isomers in these three families); 2'-alkoxyalkyl; and 2'-NMA (N -methylacetamide).

[0290] Other modifications include 2'-methoxy (2'-OCH3). 2'-aminopropoxy (2'-OCH2CH2CH2NH2) and 2'- fluoro (2'-F). Similar modifications can also be made at other positions on the RNA of an iRNA, particularly the 3' position of the sugar on the 3' terminal nucleotide or in 2'-5' linked dsRNAs and the 5' position of 5' terminal nucleotide. iRNAs can also have sugar mimetics such as cyclobutyl moieties in place of the pentofuranosyl sugar. Representative U.S. patents that teach the preparation of such modified sugar structures include, but are not limited to. U.S. Pat. Nos. 4,981,957: 5,118,800; 5.319,080; 5,359.044; 5,393,878; 5,446,137; 5,466,786; 5,514,785; 5,519,134; 5,567,811; 5,576,427; 5,591,722; 5,597,909; 5,610,300; 5,627,053; 5,639,873; 5,646,265; 5,658,873; 5,670,633; and 5,700,920, certain of which are commonly owned with the instant application. The entire contents of each of the foregoing are hereby incorporated herein by reference.

[0291] An iRNA of the invention can also include nucleobase (often referred to in the art simply as ‘“base”) modifications or substitutions. As used herein, “unmodified” or “natural” nucleobases include the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C) and uracil (U). Modified nucleobases include other synthetic and natural nucleobases such as 5-methylcytosine (5-me-C), 5- hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2 -thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil and cytosine, 5-propynyl uracil and cytosine, 6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl anal other 8- substituted adenines and guanines, 5-halo, particularly 5-bromo, 5 -trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-daazaadenine and 3 -deazaguanine and 3-deazaadenine. Further nucleobases include those disclosed in U.S. Pat. No. 3,687,808, those disclosed in Modified Nucleosides in Biochemistry, Biotechnology and Medicine, Herdewijn, P. ed. Wiley-VCH, 2008; those disclosed in The Concise Encyclopedia Of Polymer Science And Engineering, pages 858-859. Kroschwitz, J. L. ed. John Wiley & Sons. 1990, these disclosed by Englisch et al., (1991) Angewandte Chemie, International Edition, 30:613, and those disclosed by Sanghvi, Y S., Chapter 15, dsRNA Research and Applications, pages 289-302, Crooke, S. T. and Lebleu, B., Ed., CRC Press, 1993. Certain of these nucleobases are particularly useful for increasing the binding affinity of the oligomeric compounds featured in the invention. These include 5-substituted pyrimidines, 6-azapyrimidines and N-2, N-6 and 0-6 substituted purines, including 2-aminopropyladenine, 5-propynyluracil and 5- propynylcytosine. 5-methylcytosine substitutions have been shown to increase nucleic acid duplex stability by 0.6-1.2 °C (Sanghvi, Y. S., Crooke, S. T. and Lebleu, B., Eds., dsRNA Research and Applications, CRC Press, Boca Raton, 1993, pp. 276-278) and are exemplary base substitutions, even more particularly when combined with 2'-O-methoxyethyl sugar modifications.

[0292] Representative U.S. patents that teach the preparation of certain of the above noted modified nucleobases as well as other modified nucleobases include, but are not limited to, the above noted U.S. Patent Nos. 3,687,808. 4.845,205; 5,130.30; 5.134.066; 5,175,273; 5,367,066; 5.432.272; 5,457,187; 5,459,255; 5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121, 5,596,091; 5,614,617; 5,681,941; 5,750,692; 6,015,886; 6,147,200; 6,166,197; 6,222,025; 6,235,887; 6,380,368; 6,528,640; 6,639,062; 6,617,438; 7,045,610; 7,427,672; and 7,495,088, the entire contents of each of which arc hereby incorporated herein by reference. An iRNA of the invention can also be modified to include one or more locked nucleic acids (LNA). A locked nucleic acid is a nucleotide having a modified ribose moiety in which the ribose moiety comprises an extra bridge connecting the 2' and 4' carbons. This structure effectively "locks" the ribose in the 3'-endo structural conformation. The addition of locked nucleic acids to siRNAs has been shown to increase siRNA stability in serum, and to reduce off-target effects (Elmen, J. et al., (2005) Nucleic Acids Research 33(1):439- 447: Mook, OR. et al., (200T)Mol Cane Ther 6(3):833-843: Grunweller, A. et al., (2003) Nucleic Acids Research 31(12):3185-3193).

[0293] An iRNA of the invention can also be modified to include one or more bicyclic sugar moieties. A “bicyclic sugar” is a furanosyl ring modified by the bridging of two atoms. A “bicyclic nucleoside” (“BNA”) is a nucleoside having a sugar moiety comprising a bridge connecting two carbon atoms of the sugar ring, thereby forming a bicyclic ring system. In certain embodiments, the bridge connects the 4'-carbon and the 2'- carbon of the sugar ring. Thus, in some embodiments an agent of the invention may include one or more locked nucleic acids (LNA). A locked nucleic acid is a nucleotide having a modified ribose moiety in which the ribose moiety comprises an extra bridge connecting the 2' and 4' carbons. In other words, an LNA is a nucleotide comprising a bicyclic sugar moiety comprising a 4 -CH2-O-2' bridge. This structure effectively "locks" the ribose in the 3'-endo structural confomiation. The addition of locked nucleic acids to siRNAs has been shown to increase siRNA stability in serum, and to reduce off-target effects (Elmen, J. et al.. (2005) Nucleic Acids Research 33( 1 ):439-447; Mook, OR. et al., (2007) Mol Cane Ther 6(3):833-843; Grunweller. A. et al., (2003) Nucleic Acids Research 31 ( I2):3185-3193). Examples of bicyclic nucleosides for use in the polynucleotides of the invention include without limitation nucleosides comprising a bridge between the 4' and the 2' ribosyl ring atoms. In certain embodiments, the antisense polynucleotide agents of the invention include one or more bicyclic nucleosides comprising a 4' to 2' bridge. Examples of such 4' to 2' bridged bicyclic nucleosides, include but are not limited to 4'-(CH2) — O-2' (LNA); 4'-(CH2) — S-2'; 4'-(CH2)2 — O-2' (ENA); 4'-CH(CH3) — O-2' (also referred to as “constrained ethyl” or “cEt”) and 4'-CH(CH2OCH3) — O-2' (and analogs thereof: see, e.g., U.S. Pat. No. 7,399,845); 4'-C(CH3)(CH3) — O-2' (and analogs thereof: see e.g., US Patent No. 8,278,283); 4'-CH2— N(OCH3)-2' (and analogs thereof; see e.g., US Patent No. 8,278,425); 4'-CH2O N(CH3)-2' (see, e.g., U.S. Patent Publication No. 2004 / 0171570); 4'-CH2N(R) O-2', wherein R is H, C1-C12 alkyl, or a protecting group (see, e.g., U.S. Pat. No. 7,427,672); 4'-CH2— C(H)(CH3)-2' (see, e.g.. Chattopadhyaya et al., J. Org. Chem., 2009, 74, 118-134); and 4'-CH2— C(=CH2)-2' (and analogs thereof; see, e.g.. US Patent No. 8.278.426). The entire contents of each of the foregoing are hereby incorporated herein by reference.

[0294] Additional representative U.S. Patents and US Patent Publications that teach the preparation of locked nucleic acid nucleotides include, but arc not limited to, the following: U.S. Patent Nos. 6,268,490; 6,525,191; 6,670,461; 6,770,748; 6.794,499; 6,998,484; 7,053,207; 7,034, 133;7, 084, 125; 7,399,845; 7,427,672; 7,569,686; 7,741,457; 8,022,193; 8,030,467; 8,278,425; 8,278,426; 8,278,283; US 2008 / 0039618; and US 2009 / 0012281, the entire contents of each of which are hereby incorporated herein by reference.

[0295] Any of the foregoing bicyclic nucleosides can be prepared having one or more stereochemical sugar configurations including for example a-L-ribofuranose and β-D-ribofuranose (see WO 99 / 14226).

[0296] An iRNA of the invention can also be modified to include one or more constrained ethyl nucleotides. As used herein, a "constrained ethyl nucleotide" or "cEt" is a locked nucleic acid comprising a bicyclic sugar moiety comprising a 4'-CH(CH3)-0-2' bridge. In one embodiment, a constrained ethyl nucleotide is in the S conformation referred to herein as “S-cEt.”

[0297] An iRNA of the invention may also include one or more “conformationally restricted nucleotides'' (“CRN”). CRN are nucleotide analogs with a linker connecting the C2'and C4' carbons of ribose or the C3 and -C5' carbons of ribose. CRN lock the ribose ring into a stable conformation and increase the hybridization affinity to mRNA. The linker is of sufficient length to place the oxygen in an optimal position for stability and affinity resulting in less ribose ring puckering.

[0298] Representative publications that teach the preparation of certain of the above noted CRN include, but are not limited to, US Patent Publication No. 2013 / 0190383; and PCT publication WO 2013 / 036868, the entire contents of each of which are hereby incorporated herein by reference.

[0299] In some embodiments, an iRNA of the invention comprises one or more monomers that are UNA (unlocked nucleic acid) nucleotides. UNA is unlocked acyclic nucleic acid, wherein any of the bonds of the sugar has been removed, forming an unlocked "sugar" residue. In one example, UNA also encompasses monomer with bonds between CT-C4' have been removed (i.e. the covalent carbon-oxygen-carbon bond between the CT and C4' carbons). In another example, the C2'-C3' bond (i.e. the covalent carbon-carbon bond between the C2' and C3' carbons) of the sugar has been removed (see Nuc. Acids Symp. Series, 52, 133-134 (2008) and Fluiter et al.. Mol. Biosyst.. 2009, 10, 1039 hereby incorporated by reference).

[0300] Representative U.S. publications that teach the preparation of UNA include, but are not limited to, US Patent No. 8,314,227; and US Patent Publication Nos. 2013 / 0096289; 2013 / 0011922; and 2011 / 0313020, the entire contents of each of which are hereby incorporated herein by reference.

[0301] An RNAi agent of the disclosure may also include one or more “cyclohexene nucleic acids” or (“CeNA”). CeNA are nucleotide analogs with a replacement of tire furanose moiety of DNA by a cyclohexene ring. Incorporation of cylcohexenyl nucleosides in a DNA chain increases the stability of a DNA / RNA hybrid. CeNA is stable against degradation in serum and a CeNA / RNA hybrid is able to activate E. Coli RNase H, resulting in cleavage of the RNA strand. (See Wang et al., Am. Chem. Soc. 2000, 122, 36, 8595-8602, hereby incorporated by reference).

[0302] Potentially stabilizing modifications to the ends of RNA molecules can include N- (acetylaminocaproyl)-4-hydroxyprolinol (Hyp-C6-NHAc), N-(caproyl-4-hydroxyprolinol (Hyp-C6), N- (acetyl-4-hydroxyprolinol (Elyp-NHAc), thymidine-2'-0-deoxythymidine (ether), N-(aminocaproyl)-4- hydroxyprolinol (Hyp-C6-amino). 2-docosanoyl-uridine-3"- phosphate, inverted base dT(idT) and others. Disclosure of this modification can be found in PCT Publication No. WO 2011 / 005861.

[0303] Other modifications of an iRNA of the invention include a 5' phosphate or 5' phosphate mimic, e.g., a 5'-tenninal phosphate or phosphate mimic on tire antisense strand of an RNAi agent. Suitable phosphate mimics are disclosed in, for example US Patent Publication No. 2012 / 0157511, the entire contents of which are incorporated herein by reference.

[0304] In certain specific embodiments, an RNAi agent of the present invention is an agent that inhibits the expression of an AASS gene which is selected from the group of agents listed in Tables 3-6. Any of these agents may further comprise a ligand.

[0305] A. Modified iRNAs Comprising Motifs of the Invention

[0306] In certain aspects of the invention, tire double stranded RNAi agents of the invention include agents with chemical modifications as disclosed, for example, in WO 2013 / 075035, filed on November 16, 2012, the entire contents of which are incorporated herein by reference.

[0307] Accordingly, the invention provides double stranded RNAi agents capable of inhibiting the expression of a target gene (z. e.. an AASS gene) in vivo. Tire RNAi agent comprises a sense strand and an antisense strand. Each strand of the RNAi agent may range from 12-30 nucleotides in length. For example, each strand may be between 14-30 nucleotides in length, 17-30 nucleotides in length, 25-30 nucleotides in length. 27-30 nucleotides in length, 17-23 nucleotides in length, 17-21 nucleotides in length, 17-19 nucleotides in length, 19-25 nucleotides in length, 19-23 nucleotides in length, 19-21 nucleotides in length, 21-25 nucleotides in length, or 21-23 nucleotides in length. In one embodiment, tire sense strand is 21 nucleotides in length. In one embodiment, the antisense strand is 23 nucleotides in length.

[0308] The sense strand and antisense strand typically form a duplex double stranded RNA ( 'dsRN A”), also referred to herein as an "RNAi agent.” The duplex region of an RNAi agent may be 12-30 nucleotide pairs in length. For example, the duplex region can be between 14-30 nucleotide pairs in length, 17-30 nucleotide pairs in length, 27-30 nucleotide pairs in length, 17 - 23 nucleotide pairs in length, 17-21 nucleotide pairs in length, 17-19 nucleotide pairs in length, 19-25 nucleotide pairs in length, 19-23 nucleotide pairs in length, 19- 21 nucleotide pairs in length, 21-25 nucleotide pairs in length, or 21-23 nucleotide pairs in length. In another example, the duplex region is selected from 15, 16, 17, 18, 19, 20. 21, 22, 23, 24, 25, 26, and 27 nucleotides in length.

[0309] In one embodiment, the RNAi agent may contain one or more overhang regions and / or capping groups at the 3 '-end, 5 '-end, or both ends of one or both strands. The overhang can be 1-6 nucleotides in length, for instance 2-6 nucleotides in length, 1-5 nucleotides in length, 2-5 nucleotides in length, 1-4 nucleotides in length, 2-4 nucleotides in length, 1-3 nucleotides in length, 2-3 nucleotides in length, or 1-2 nucleotides in length. The overhangs can be the result of one strand being longer than the other, or the result of two strands of the same length being staggered. The overhang can form a mismatch with the target mRNA or it can be complementary to the gene sequences being targeted or can be another sequence. The first and second strands can also be joined, e.g., by additional bases to form a hairpin, or by other non-base linkers.

[0310] In one embodiment, the nucleotides in the overhang region of the RNAi agent can each independently be a modified or unmodified nucleotide including, but no limited to 2'-sugar modified, such as, 2-F. 2'- Omethyl, thymidine (T). 2 -O-methoxyethyl-5-methyluridine (Teo). 2' -O-methoxyethyladenosine (Aeo), 2 - O-mcthoxycthyl-5-methylcytidine (m5Ceo), and any combinations thereof. For example, TT can be an overhang sequence for either end on either strand. The overhang can form a mismatch with the target mRNA or it can be complementary to the gene sequences being targeted or can be another sequence.

[0311] The 5'- or 3'- overhangs at the sense strand, antisense strand or both strands of the RNAi agent may be phosphorylated. In some embodiments, the overhang region(s) contains two nucleotides having a phosphorothioate betw een the two nucleotides, where the two nucleotides can be the same or different. In one embodiment, the overhang is present at the 3 '-end of the sense strand, antisense strand, or both strands. In one embodiment, this 3'-overhang is present in the antisense strand. In one embodiment, this 3'-overhang is present in the sense strand.

[0312] The RNAi agent may contain only a single overhang, which can strengthen the interference activity of the RNAi, without affecting its overall stability. For example, the single -stranded overhang may be located at the 3'-terminal end of the sense strand or, alternatively, at the 3'-terminal end of the antisense strand. The RNAi may also have a blunt end, located at the 5 '-end of the antisense strand (or the 3 '-end of the sense strand) or vice versa. Generally, the antisense strand of the RNAi has a nucleotide overhang at the 3 '-end, and the 5 '-end is blunt. While not wishing to be bound by theory, the asymmetric blunt end at tire 5 '-end of the antisense strand and 3 '-end overhang of the antisense strand favor the guide strand loading into RISC process.

[0313] In one embodiment, the RNAi agent is a double ended bluntmer of 19 nucleotides in length, wherein the sense strand contains at least one motif of three 2'-F modifications on three consecutive nucleotides at positions 7, 8, 9 from the 5 'end. The antisense strand contains at least one motif of three 2'-O-methyl modifications on three consecutive nucleotides at positions 11, 12, 13 from the 5 'end.

[0314] In another embodiment, the RNAi agent is a double ended bluntmer of 20 nucleotides in length, wherein the sense strand contains at least one motif of three 2 -F modifications on three consecutive nucleotides at positions 8, 9. 10 from the 5 'end. The antisense strand contains at least one motif of three 2'-O- methyl modifications on three consecutive nucleotides at positions I I. 12. 13 from the 5 'end.

[0315] In yet another embodiment, the RNAi agent is a double ended bluntmer of 21 nucleotides in length, wherein the sense strand contains at least one motif of three 2'-F modifications on three consecutive nucleotides at positions 9, 10, 11 from the 5'cnd. The antisense strand contains at least one motif of three 2'- O-methyl modifications on three consecutive nucleotides at positions 11, 12, 13 from the 5'end. In one embodiment, the RNAi agent comprises a 21 nucleotide sense strand and a 23 nucleotide antisense strand, wherein the sense strand contains at least one motif of three 2'-F modifications on three consecutive nucleotides at positions 9, 10, 11 from the 5 'end; the antisense strand contains at least one motif of three 2'-O-methyl modifications on three consecutive nucleotides at positions 11. 12, 13 from the 5'end, wherein one end of the RNAi agent is blunt, while the other end comprises a 2 nucleotide overhang. Preferably, the 2 nucleotide overhang is at the 3 '-end of the antisense strand.

[0316] When the 2 nucleotide overhang is at the 3 '-end of the antisense strand, there may be two phosphorothioate intemucleotide linkages between the terminal three nucleotides, wherein two of the three nucleotides are the overhang nucleotides, and the third nucleotide is a paired nucleotide next to the overhang nucleotide. In one embodiment, tire RNAi agent additionally has two phosphorothioate intemucleotide linkages between the tenninal three nucleotides at both the 5 '-end of the sense strand and at the 5 '-end of the antisense strand. In one embodiment, every nucleotide in the sense strand and the antisense strand of the RNAi agent, including the nucleotides that are part of the motifs are modified nucleotides. In one embodiment each residue is independently modified with a 2'-O-methyl or 3 '-fluoro, e.g., in an alternating motif. Optionally, the RNAi agent further comprises a ligand (preferably GalNAcs).

[0317] In one embodiment, the RNAi agent comprises a sense and an antisense strand, wherein the sense strand is 25-30 nucleotide residues in length, wherein starting from the 5' terminal nucleotide (position 1) positions 1 to 23 of the first strand comprise at least 8 ribonucleotides; the antisense strand is 36-66 nucleotide residues in length and, starting from the 3' terminal nucleotide, comprises at least 8 ribonucleotides in the positions paired with positions 1- 23 of sense strand to form a duplex; wherein at least the 3 ' terminal nucleotide of antisense strand is unpaired with sense strand, and up to 6 consecutive 3' terminal nucleotides are unpaired with sense strand, thereby fonning a 3' single stranded overhang of 1-6 nucleotides; wherein the 5' terminus of antisense strand comprises from 10-30 consecutive nucleotides which are unpaired with sense strand, thereby forming a 10-30 nucleotide single stranded 5' overhang; wherein at least the sense strand 5' terminal and 3' terminal nucleotides are base paired with nucleotides of antisense strand when sense and antisense strands are aligned for maximum complementarity, thereby forming a substantially duplexed region between sense and antisense strands; and antisense strand is sufficiently complementary to a target RNA along at least 19 ribonucleotides of antisense strand length to reduce target gene expression when the double stranded nucleic acid is introduced into a mammalian cell; and wherein the sense strand contains at least one motif of three 2'-F modifications on three consecutive nucleotides, where at least one of the motifs occurs at or near the cleavage site. The antisense strand contains at least one motif of three 2'-O-methyl modifications on three consecutive nucleotides at or near the cleavage site.

[0318] In one embodiment, the RNAi agent comprises sense and antisense strands, wherein the RNAi agent comprises a first strand having a length which is at least 25 and at most 29 nucleotides and a second strand having a length which is at most 30 nucleotides with at least one motif of three 2'-O-methyl modifications on three consecutive nucleotides at position 11, 12, 13 from the 5' end: wherein the 3' end of the first strand and the 5' end of the second strand form a blunt end and the second strand is 1-4 nucleotides longer at its 3' end than the first strand, wherein the duplex region which is at least 25 nucleotides in length, and the second strand is sufficiently complementary to a target mRNA along at least 19 nucleotide of the second strand length to reduce target gene expression when the RNAi agent is introduced into a mammalian cell, and wherein dicer cleavage of the RNAi agent preferentially results in an siRNA comprising the 3 ' end of the second strand, thereby reducing expression of the target gene in the mammal. Optionally, the RNAi agent further comprises a ligand.

[0319] In one embodiment, the sense strand of the RNAi agent contains at least one motif of three identical modifications on three consecutive nucleotides, where one of the motifs occurs at tire cleavage site in the sense strand.

[0320] In one embodiment, the antisense strand of the RNAi agent can also contain at least one motif of three identical modifications on three consecutive nucleotides, where one of the motifs occurs at or near the cleavage site in the antisense strand.

[0321] For an RNAi agent having a duplex region of 17-23 nucleotide in length, the cleavage site of the antisense strand is typically around the 10, 11 and 12 positions from the 5 '-end. Tims the motifs of three identical modifications may occur at the 9, 10, 11 positions; 10, 11, 12 positions; 11, 12, 13 positions: 12, 13, 14 positions; or 13, 14, 15 positions of the antisense strand, the count starting from the 1stnucleotide from the 5 '-end of the antisense strand, or, the count starting from the 1stpaired nucleotide within the duplex region from the 5'- end of the antisense strand. The cleavage site in the antisense strand may also change according to the length of the duplex region of tire RNAi from the 5 '-end.

[0322] The sense strand of tire RNAi agent may contain at least one motif of three identical modifications on three consecutive nucleotides at the cleavage site of the strand; and the antisense strand may have at least one motif of three identical modifications on three consecutive nucleotides at or near the cleavage site of the strand. When the sense strand and the antisense strand form a dsRNA duplex, the sense strand and the antisense strand can be so aligned that one motif of the three nucleotides on the sense strand and one motif of the three nucleotides on the antisense strand have at least one nucleotide overlap, i. e. , at least one of the three nucleotides of the motif in the sense strand forms a base pair with at least one of the three nucleotides of the motif in the antisense strand. Alternatively, at least two nucleotides may overlap, or all three nucleotides may overlap.

[0323] In one embodiment, the sense strand of the RNAi agent may contain more than one motif of three identical modifications on three consecutive nucleotides. Tire first motif may occur at or near the cleavage site of the strand and the other motifs may be a wing modification. The term “wing modification” herein refers to a motif occurring at another portion of the strand that is separated from the motif at or near the cleavage site of the same strand. The wing modification is either adjacent to tire first motif or is separated by at least one or more nucleotides. When the motifs are immediately adjacent to each other then the chemistry7of the motifs are distinct from each other and when tire motifs are separated by one or more nucleotide than the chemistries can be the same or different. Two or more wing modifications may be present. For instance, when two wing modifications are present, each wing modification may occur at one end relative to the first motif which is at or near cleavage site or on either side of the lead motif.

[0324] Like the sense strand, the antisense strand of the RNAi agent may contain more than one motifs of three identical modifications on three consecutive nucleotides, with at least one of the motifs occurring at or near the cleavage site of the strand. This antisense strand may also contain one or more wing modifications in an alignment similar to the wing modifications that may be present on the sense strand.

[0325] In one embodiment, the wing modification on the sense strand or antisense strand of the RNAi agent typically does not include the first one ortwo terminal nucleotides at tire 3'-end, 5'-end or both ends of the strand.

[0326] In another embodiment, the wing modification on the sense strand or antisense strand of the RNAi agent typically does not include the first one or two paired nucleotides within the duplex region at the 3 '-end, 5 '-end or both ends of the strand.

[0327] When the sense strand and the antisense strand of the RNAi agent each contain at least one wing modification, the wing modifications may fall on the same end of the duplex region, and have an overlap of one. two or three nucleotides.

[0328] When the sense strand and the antisense strand of the RNAi agent each contain at least two wing modifications, the sense strand and the antisense strand can be so aligned that two modifications each from one strand fall on one end of the duplex region, having an overlap of one, tw o or three nucleotides; two modifications each from one strand fall on the other end of tire duplex region, having an overlap of one, two or three nucleotides; tw o modifications one strand fall on each side of the lead motif, having an overlap of one, two or three nucleotides in tire duplex region.

[0329] In one embodiment, every nucleotide in the sense strand and antisense strand of the RNAi agent, including the nucleotides that are part of the motifs, may be modified. Each nucleotide may be modified with the same or different modification which can include one or more alteration of one or both of the non-linking phosphate oxygens and / or of one or more of the linking phosphate oxygens; alteration of a constituent of the ribose sugar, e.g., of the 2' hydroxyl on the ribose sugar: wholesale replacement of the phosphate moiety with "dcphospho" linkers: modification or replacement of a naturally occurring base; and replacement or modification of the ribose-phosphate backbone.

[0330] As nucleic acids are polymers of subunits, many of the modifications occur at a position w7hich is repeated w ithin a nucleic acid, e.g., a modification of a base, or a phosphate moiety, or a non-linking 0 of a phosphate moiety. In some cases, the modification will occur at all of the subject positions in the nucleic acid but in many cases it will not. By way of example, a modification may only occur at a 3 ' or 5 ' terminal position, may only occur in a terminal region, e.g., at a position on a terminal nucleotide or in the last 2, 3, 4, 5, or 10 nucleotides of a strand. A modification may occur in a double strand region, a single strand region, or in both. A modification may occur only in the double strand region of a RNA or may only occur in a single strand region of a RNA. For example, a phosphorothioate modification at a non-linking 0 position may only occur at one or both termini, may only occur in a terminal region, e.g., at a position on a terminal nucleotide or in the last 2. 3, 4, 5, or 10 nucleotides of a strand, or may occur in double strand and single strand regions, particularly at termini. The 5' end or ends can be phosphorylated.

[0331] It may be possible, e.g., to enhance stability , to include particular bases in overhangs, or to include modified nucleotides or nucleotide surrogates, in single strand overhangs, e.g., in a 5' or 3' overhang, or in both. For example, it can be desirable to include purine nucleotides in overhangs. In some embodiments all or some of the bases in a 3' or 5' overhang may be modified, e.g., with a modification described herein. Modifications can include, e.g., the use of modifications at the 2' position of the ribose sugar with modifications that are known in the art, e.g., the use of deoxyribonucleotides, 2'- deoxy-2' -fluoro (2'-F) or 2'-O-methyl modified instead of the ribosugar of the nucleobase, and modifications in the phosphate group, e.g., phosphorothioate modifications. Overhangs need not be homologous with the target sequence.

[0332] In one embodiment, each residue of the sense strand and antisense strand is independently modified with LNA, CRN, cET, UNA, HNA, CeNA, 2'-methoxyethyl, 2'- O-methyl, 2'-O-allyl, 2 -C- allyl, 2'-deoxy, 2'-hydroxyl, or 2'-fluoro. The strands can contain more than one modification. In one embodiment, each residue of the sense strand and antisense strand is independently modified with 2'- O-methyl or 2'-fluoro. The term “HNA" refers to hexitol or hexose nucleic acid.

[0333] At least two different modifications are typically present on the sense strand and antisense strand. Those two modifications may be the 2'- O-methyl or 2 '-fluoro modifications, or others.

[0334] In one embodiment, the Naand / or Nb comprise modifications of an alternating pattern. The term “alternating motif' as used herein refers to a motif having one or more modifications, each modification occurring on alternating nucleotides of one strand. The alternating nucleotide may refer to one per every other nucleotide or one per every three nucleotides, or a similar pattern. For example, if A, B and C each represent one type of modification to the nucleotide, the alternating motif can be “ABABABABABAB ... ,'' “AABBAABBAABB . . .,'' “AABAABAABAAB . . .” “AAABAAABAAAB . .. ,” “AAABBBAAABBB ... ” or “ABCABCABCABC... ,” etc.

[0335] The type of modifications contained in the alternating motif may be the same or different. For example, if A, B, C, D each represent one type of modification on the nucleotide, the alternating pattern, i.e., modifications on every other nucleotide, may be the same, but each of the sense strand or antisense strand can be selected from several possibilities of modifications within the alternating motif such as “AB AB AB ... ”, “ACACAC ... ” “BDBDBD ... ” or “CDCDCD ... etc.

[0336] In one embodiment, the RNAi agent of the invention comprises the modification pattern for the alternating motif on the sense strand relative to the modification pattern for the alternating motif on the antisense strand is shifted. The shift may be such that the modified group of nucleotides of the sense strand corresponds to a differently modified group of nucleotides of the antisense strand and vice versa. For example, the sense strand when paired with the antisense strand in the dsRNA duplex, the alternating motif in the sense strand may start with “ABABAB” from 5 '-3' of the strand and the alternating motif in the antisense strand may start with “BAB AB A” from 5 '-3 'of the strand within the duplex region. As another example, the alternating motif in the sense strand may start with “AABBAABB” from 5 '-3' of the strand and the alternating motif in the antisense strand may start with “BBAABBAA” from 5 ‘-3' of the strand within the duplex region, so that there is a complete or partial shift of the modification patterns between the sense strand and the antisense strand.

[0337] In one embodiment, the RNAi agent comprises the pattern of the alternating motif of 2'-O-methyl modification and 2'-F modification on tire sense strand initially has a shift relative to the pattern of the alternating motif of 2'-O-methyl modification and 2'-F modification on the antisense strand initially, i.e., the 2'-O-methyl modified nucleotide on the sense strand base pairs with a 2'-F modified nucleotide on the antisense strand and vice versa. The 1 position of the sense strand may start with the 2'-F modification, and the 1 position of the antisense strand may start with the 2'- O-methyl modification.

[0338] The introduction of one or more motifs of three identical modifications on three consecutive nucleotides to the sense strand and / or antisense strand interrupts the initial modification pattern present in the sense strand and / or antisense strand. This interruption of the modification pattern of the sense and / or antisense strand by introducing one or more motifs of three identical modifications on three consecutive nucleotides to the sense and / or antisense strand surprisingly enhances the gene silencing activity to the target gene.

[0339] In one embodiment, when the motif of three identical modifications on three consecutive nucleotides is introduced to any of the strands, the modification of tire nucleotide next to the motif is a different modification than the modification of the motif. For example, the portion of the sequence containing tire motif is “. . .NaYYYNb. . . ,” where "Y" represents tire modification of the motif of three identical modifications on three consecutive nucleotide, and “Na” and “Nb” represent a modification to the nucleotide next to the motif “ YYY” that is different than the modification of Y, and where Naand Nb can be the same or different modifications. Alternatively, Naand / or Nb may be present or absent when there is a wing modification present.

[0340] Tire RNAi agent may further comprise at least one phosphorothioatc or mcthylphosphonatc intemucleotide linkage. The phosphorothioate or methylphosphonate intemucleotide linkage modification may occur on any nucleotide of the sense strand or antisense strand or both strands in any position of the strand. For instance, the intemucleotide linkage modification may occur on every nucleotide on the sense strand and / or antisense strand; each intemucleotide linkage modification may occur in an alternating pattern on the sense strand and / or antisense strand; or the sense strand or antisense strand may contain both intemucleotide linkage modifications in an alternating pattern. Tire alternating pattern of the intemucleotide linkage modification on the sense strand may be the same or different from the antisense strand, and the alternating pattern of the intemucleotide linkage modification on the sense strand may have a shift relative to the alternating pattern of the intemucleotide linkage modification on the antisense strand. In one embodiment, a double-stranded RNAi agent comprises 6-8 phosphorothioate intemucleotide linkages. In one embodiment, the antisense strand comprises two phosphorothioate intemucleotide linkages at the 5 '-terminus and two phosphorothioate intemucleotide linkages at the 3 '-terminus, and the sense strand comprises at least two phosphorothioate intemucleotide linkages at either tire 5 '-terminus or the 3 '-terminus.

[0341] In one embodiment, the RNAi comprises a phosphorothioate or methylphosphonate intemucleotide linkage modification in the overhang region. For example, the overhang region may contain two nucleotides having a phosphorothioate or methylphosphonate intemucleotide linkage between the two nucleotides. Intemucleotide linkage modifications also may be made to link the overhang nucleotides with the terminal paired nucleotides within tire duplex region. For example, at least 2, 3, 4, or all the overhang nucleotides may be linked through phosphorothioate or methylphosphonate intemucleotide linkage, and optionally, there may be additional phosphorothioate or methylphosphonate intemucleotide linkages linking the overhang nucleotide with a paired nucleotide that is next to the overhang nucleotide. For instance, there may be at least two phosphorothioate intemucleotide linkages between the terminal three nucleotides, in which two of the three nucleotides are overhang nucleotides, and the third is a paired nucleotide next to the overhang nucleotide. These terminal three nucleotides may be at the 3 '-end of the antisense strand, tire 3 '-end of the sense strand, the 5 '-end of the antisense strand, and / or tire 5 'end of the antisense strand.

[0342] In one embodiment, the 2 nucleotide overhang is at the 3 '-end of the antisense strand, and there are two phosphorothioate intemucleotide linkages between the terminal three nucleotides, wherein two of the three nucleotides are the overhang nucleotides, and the third nucleotide is a paired nucleotide next to the overhang nucleotide. Optionally, the RNAi agent may additionally have two phosphorothioate intemucleotide linkages between the terminal three nucleotides at both the 5 '-end of the sense strand and at the 5 '-end of the antisense strand.

[0343] In one embodiment, the RNAi agent comprises mismatch(es) with the target, within the duplex, or combinations thereof. The mismatch may occur in the overhang region or the duplex region. The base pair may be ranked on the basis of their propensity to promote dissociation or melting (e.g. , on the free energy of association or dissociation of a particular pairing, the simplest approach is to examine the pairs on an individual pair basis, though next neighbor or similar analysis can also be used). In terms of promoting dissociation: A:U is preferred over G:C; G:U is preferred over G:C; and I:C is preferred over G:C (I=inosine). Mismatches, e.g., non-canonical or other than canonical pairings (as described elsewhere herein) are preferred over canonical (A:T, A:U, G:C) pairings; and pairings which include a universal base are preferred over canonical pairings.

[0344] In one embodiment, the RNAi agent comprises at least one of the first 1, 2, 3, 4. or 5 base pairs within the duplex regions from the 5'- end of the antisense strand independently selected from the group of: A:U, G:U, I:C, and mismatched pairs, e.g., non-canonical or other than canonical pairings or pairings which include a universal base, to promote the dissociation of the antisense strand at the 5 '-end of the duplex.

[0345] In one embodiment, the nucleotide at the 1 position within the duplex region from the 5 '-end in the antisense strand is selected from the group consisting of A, dA, dU, U, and dT. Alternatively, at least one of the first 1, 2 or 3 base pair within the duplex region from the 5' - end of the antisense strand is an AU base pair. For example, tire first base pair within the duplex region from the 5'- end of the antisense strand is an AU base pair.

[0346] In another embodiment, the nucleotide at the 3 '-end of the sense strand is deoxy-thymine (dT). In another embodiment, the nucleotide at the 3 '-end of the antisense strand is deoxy-thymine (dT). In one embodiment, there is a short sequence of deoxy-thymine nucleotides, for example, two dT nucleotides on the 3 '-end of the sense and / or antisense strand.

[0347] In one embodiment, the sense strand sequence may be represented by formula (I):

[0348] 5' np-Na-(X X X )i-Nb-Y Y Y -Nb-(Z Z Z )j-Na-nq3' (I) wherein: i and j are each independently 0 or 1 ; p and q are each independently 0-6; each Naindependently represents an oligonucleotide sequence comprising 0-25 modified nucleotides, each sequence comprising at least two differently modified nucleotides; each Nb independently represents an oligonucleotide sequence comprising 0-10 modified nucleotides; each npand nqindependently represent an overhang nucleotide; wherein Nb and Y do not have the same modification; and

[0349] XXX, YYY and ZZZ each independently represent one motif of three identical modifications on three consecutive nucleotides. Preferably YYY is all 2'-F modified nucleotides.

[0350] In one embodiment, the Naand / or Nbcomprise modifications of alternating pattern.

[0351] In one embodiment, the YYY motif occurs at or near the cleavage site of the sense strand. For example, when the RNAi agent has a duplex region of 17-23 nucleotides in length, the YYY motif can occur at or the vicinity of the cleavage site (e.g. : can occur at positions 6, 7, 8, 7, 8, 9, 8, 9, 10, 9, 10, 11, 10, 11,12 or 11, 12, 13) of the sense strand, the count starting from the 1stnucleotide, from the 5'-end; or optionally, the count starting at the 1stpaired nucleotide within the duplex region, from the 5'- end. In one embodiment, i is 1 and j is 0, or i is 0 and j is 1 , or both i and j are 1. Tire sense strand can therefore be represented by the following formulas:

[0352] 5' np-Na-YYY-Nb-ZZZ-Na-nq3' (lb);

[0353] 5' np-Na-XXX-Nb-YYY-Na-nq3' (Ic); or

[0354] 5' np-Na-XXX-Nb-YYY-Nb-ZZZ-Na-nq3' (Id).

[0355] When the sense strand is represented by formula (lb), Nb represents an oligonucleotide sequence comprising 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each Naindependently can represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0356] When the sense strand is represented as formula (Ic), Nb represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each Nacan independently represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0357] When the sense strand is represented as formula (Id), each Nb independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Preferably, Nb is 0, 1, 2, 3, 4, 5 or 6. Each Nacan independently represent an oligonucleotide sequence comprising 2-20, 2-15, or 2- 10 modified nucleotides.

[0358] Each of X, Y and Z may be the same or different from each other.

[0359] In other embodiments, i is 0 and j is 0, and the sense strand may be represented by the formula:

[0360] 5' np-Na-YYY- Na-nq3' (la).

[0361] When the sense strand is represented by formula (la), each Naindependently can represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0362] In one embodiment, the antisense strand sequence of tire RNAi may be represented by fonnula (le):

[0363] 5' nq-Na'-(Z'Z'Z')k-Nb'-Y'¥'Y'-Nb'-(X'X'X')i-N'a-np' 3' (le) wherein: k and 1 are each independently 0 or 1 ; p' and q' are each independently 0-6; each Na' independently represents an oligonucleotide sequence comprising 0-25 modified nucleotides, each sequence comprising at least two differently modified nucleotides; each Nb' independently represents an oligonucleotide sequence comprising 0-10 modified nucleotides; each np' and nq' independently represent an overhang nucleotide; wherein Nb' and Y' do not have the same modification; and

[0364] X'X'X', YY'Y' and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides.

[0365] In one embodiment, the Na' and / or Nb' comprise modifications of alternating pattern. The Y'Y'Y' motif occurs at or near the cleavage site of the antisense strand. For example, when the RNAi agent has a duplex region of 17-23nucleotidein length, the YYY' motif can occur at positions 9, 10, 11;10, 11, 12; 11, 12, 13; 12, 13, 14; or 13, 14, 15 of the antisense strand, with the count starting from the 1stnucleotide, from the 5 '-end; or optionally, the count starting at the 1stpaired nucleotide within tire duplex region, from the 5'- end. Preferably, the Y'Y'Y' motif occurs at positions 11, 12, 13.

[0366] In one embodiment. Y'Y'Y' motif is all 2'-OMe modified nucleotides.

[0367] In one embodiment, k is 1 and 1 is 0, or k is 0 and 1 is 1, or both k and 1 are 1.

[0368] The antisense strand can therefore be represented by the following formulas:

[0369] 5' na'- Na'-Z'Z'Z'-Nb'-Y'Y'Y'-Na'-np'- 3' (Ig);

[0370] 5' na'- Na'-Y'Y'Y'-Nb'-X'X'X'-np' 3' (Ih); or

[0371] 5' na'- Na'- Z'Z'Z'-Nb'-Y'Y'Y'-Nb'- X'X'X'-Na'-np- 3' (li).

[0372] When the antisense strand is represented by formula (Ig), Nb represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each Na' independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0373] When the antisense strand is represented as formula (Ih), Nb' represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each Na' independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0374] When the antisense strand is represented as formula (li), each Nb' independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each Na' independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides. Preferably, Nb is 0, 1, 2, 3, 4, 5 or 6.

[0375] In other embodiments, k is 0 and 1 is 0 and the antisense strand may be represented by the formula:

[0376] 5' np'-Na'-Y'Y'Y'- Na'-nq- 3' (If).

[0377] When the antisense strand is represented as formula (If), each Na' independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0378] Each of X', Y' and Z' may be the same or different from each other.

[0379] Each nucleotide of the sense strand and antisense strand may be independently modified with LNA, CRN, UNA, cEt, HNA, CeNA, 2 '-methoxyethyl, 2'-O-methyl, 2'-O-allyl. 2'-C- allyl, 2'-hydroxyl, or 2'- fluoro. For example, each nucleotide of the sense strand and antisense strand is independently modified with 2'-O-methyl or 2'-fluoro. Each X, Y. Z, X'. Y' and Z', in particular, may represent a 2'-O-methyl modification or a 2'-fluoro modification.

[0380] In one embodiment, the sense strand of the RNAi agent may contain YYY motif occurring at 9, 10 and 11 positions of the strand when the duplex region is 21 nt, the count starting from the 1stnucleotide from the 5 '-end, or optionally, the count starting at the 1stpaired nucleotide within the duplex region, from the 5'- end; and Y represents 2'-F modification. The sense strand may additionally contain XXX motif or ZZZ motifs as wing modifications at the opposite end of the duplex region; and XXX and ZZZ each independently represents a 2'-0Me modification or 2'-F modification.

[0381] In one embodiment the antisense strand may contain Y'Y'Y' motif occurring at positions 11, 12, 13 of the strand, the count starting from the 1st nucleotide from the 5' end, or optionally, the count starting at the 1st paired nucleotide within the duplex region, from the 5'- end; and Y' represents 2'-O-methyl modification. The antisense strand may additionally contain X'X'X' motif or Z'Z'Z' motifs as wing modifications at the opposite end of the duplex region; and X'X'X' and Z'Z'Z' each independently represents a 2'-OMc modification or 2'-F modification.

[0382] Tire sense strand represented by any one of the above formulas (la), (lb), (Ic), and (Id) forms a duplex with an antisense strand being represented by any one of formulas (If), (Ig), (Ih), and (li), respectively.

[0383] Accordingly, the RNAi agents for use in tire methods of the invention may comprise a sense strand and an antisense strand, each strand having 14 to 30 nucleotides, the RNAi duplex represented by formula (Ij): sense : 5 ' np -Na-(X X X)i -Nb- Y Y Y -Nb -(Z Z Z)j -Na-nq 3 ' antisense: 3' np'-Na'-(X'X'X')k-Nb'-Y'Y'Y'-Nb'-(Z'Z'Z')l-Na'-nq' 5'

[0384] (Ij) wherein: i, j, k, and 1 are each independently 0 or 1; p. p', q, and q' are each independently 0-6; each Na and Na' independently represents an oligonucleotide sequence comprising 0-25 modified nucleotides, each sequence comprising at least two differently modified nucleotides; each Nb and Nb' independently represents an oligonucleotide sequence comprising 0-10 modified nucleotides; wherein each np'. np, nq', and nq, each of which may or may not be present, independently represents an overhang nucleotide; and

[0385] XXX, YYY, ZZZ , X'X'X', Y'Y'Y', and Z'Z'Z' each independently represent one motif of three identical modifications on three consecutive nucleotides.

[0386] In one embodiment, i is 0 and j is 0; or i is 1 and j is 0; or i is 0 and j is 1; or both i and j are 0; or both i and j are 1. In another embodiment, k is 0 and 1 is 0; or k is 1 and 1 is 0; k is 0 and 1 is 1 ; or both k and 1 are 0; or both k and 1 are 1.

[0387] Exemplary combinations of the sense strand and antisense strand forming a RNAi duplex include the formulas below:

[0388] 5' np - Na -Y Y Y -Na-nq 3'

[0389] 3' np' -Na' -Y'Y'Y' -Na'nq' 5' (Ik)

[0390] 5' np -Na -Y Y Y -Nb -Z Z Z -Na-nq 3'

[0391] 3' np'-Na'-Y'Y'Y'-Nb'-Z'Z'Z'-Na'nq' 5' (II) 5' np-Na- X X X -Nb -Y Y Y - Na-nq 3'

[0392] 3' np'-Na'-X'X'X'-Nb'-YY'Y'-Na'-nq' 5' (Im)

[0393] 5' np -Na -X X X -Nb-Y Y Y -Nb- Z Z Z -Na-nq 3'

[0394] 3' np'-Na'-X'X'X'-Nb'-YYY'-Nb'-Z'Z'Z'-Na-nq' 5' (In)

[0395] When the RNAi agent is represented by formula (Ik), each Na independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0396] When the RNAi agent is represented by formula (II), each Nb independently represents an oligonucleotide sequence comprising 1-10, 1-7, 1-5 or 1-4 modified nucleotides. Each Na independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0397] When the RNAi agent is represented as fonnula (Im), each Nb, Nb' independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each Na independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

[0398] When the RNAi agent is represented as formula (In), each Nb, Nb' independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or Omodified nucleotides. Each Na, Na' independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides. Each of Na, Na', Nb and Nb' independently comprises modifications of alternating pattern.

[0399] Each of X, Y and Z in formulas (Ij). (Ik), (II), (Im), and (In) may be the same or different from each other.

[0400] When the RNAi agent is represented by formula (Ij), (Ik), (II), (Im), and (In), at least one of the Y nucleotides may form a base pair with one of the Y' nucleotides. Alternatively, at least two of tire Y nucleotides form base pairs with tire corresponding Y' nucleotides; or all three of the Y nucleotides all form base pairs with tire corresponding Y' nucleotides.

[0401] When the RNAi agent is represented by formula (II) or (In), at least one of the Z nucleotides may form a base pair with one of the Z' nucleotides. Alternatively, at least two of the Z nucleotides form base pairs with the corresponding Z' nucleotides; or all three of the Z nucleotides all form base pairs with the corresponding Z' nucleotides.

[0402] When the RNAi agent is represented as formula (Im) or (In), at least one of the X nucleotides may fonn a base pair with one of the X' nucleotides. Alternatively, at least two of the X nucleotides fomi base pairs with the corresponding X' nucleotides; or all three of the X nucleotides all form base pairs with the corresponding X' nucleotides.

[0403] In one embodiment, the modification on tire Y nucleotide is different than the modification on the Y' nucleotide, the modification on the Z nucleotide is different than the modification on the Z' nucleotide, and / or the modification on the X nucleotide is different than the modification on the X‘ nucleotide.

[0404] In one embodiment, when the RNAi agent is represented by fonnula (In), the Na modifications are 2'- O-methyl or 2'-fluoro modifications. In another embodiment, when the RNAi agent is represented by formula (In), the Na modifications are 2'-O-methyl or 2'-fluoro modifications and np' >0 and at least one np' is linked to a neighboring nucleotide a via phosphorothioate linkage. In yet another embodiment, when the RNAi agent is represented by formula (In), the Na modifications are 2'-O-methyl or 2'-fluoro modifications, np' >0 and at least one np' is linked to a neighboring nucleotide via phosphorothioate linkage, and the sense strand is conjugated to one or more GalNAc derivatives attached through a bivalent ortrivalent branched linker (described below). In another embodiment, when the RNAi agent is represented by formula (In), the Na modifications are 2'-O-methyl or 2'-fluoro modifications, np' >0 and at least one np' is linked to a neighboring nucleotide via phosphorothioate linkage, the sense strand comprises at least one phosphorothioate linkage, and the sense strand is conjugated to one or more GalNAc derivatives attached through a bivalent or trivalent branched linker.

[0405] In one embodiment, when the RNAi agent is represented by formula (Ik), the Na modifications are 2'- O-methyl or 2'-fluoro modifications, np' >0 and at least one np' is linked to a neighboring nucleotide via phosphorothioate linkage, the sense strand comprises at least one phosphorothioate linkage, and the sense strand is conjugated to one or more GalNAc derivatives attached through a bivalent ortrivalent branched linker.

[0406] In one embodiment, the RNAi agent is a multimer containing at least two duplexes represented by formula (Ij), (Ik), (II), (Im), and (In), wherein the duplexes are connected by a linker. The linker can be cleavable or non-cleavable. Optionally, the multimer further comprises a ligand. Each of the duplexes can target the same gene or two different genes; or each of the duplexes can target same gene at two different target sites.

[0407] In one embodiment, the RNAi agent is a multimer containing three, four, five, six or more duplexes represented by formula (Ij), (Ik), (II), (Im), and (In), wherein the duplexes are connected by a linker. The linker can be clcavablc or non-cleavable. Optionally, the multimcr further comprises a ligand. Each of the duplexes can target the same gene or two different genes; or each of the duplexes can target same gene at two different target sites.

[0408] In one embodiment, two RNAi agents represented by formula (Ij), (Ik), (II), (Im), and (In) are linked to each other at the 5' end, and one or both of the 3' ends and are optionally conjugated to a ligand. Each of the agents can target the same gene or two different genes; or each of the agents can target same gene at two different target sites.

[0409] In certain embodiments, an RNAi agent of the invention may contain a low number of nucleotides containing a 2 ’-fluoro modification, e.g., 10 or fewer nucleotides with 2?-fluoro modification. For example, the RNAi agent may contain 10, 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0 nucleotides with a 2'-fluoro modification. In a specific embodiment, the RNAi agent of the invention contains 10 nucleotides with a 2'-fluoro modification, e.g., 4 nucleotides with a 2'-fluoro modification in the sense strand and 6 nucleotides with a 2'-fluoro modification in the antisense strand. In another specific embodiment, the RNAi agent of the invention contains 6 nucleotides with a 2'-fluoro modification, e.g., 4 nucleotides with a 2'-fluoro modification in the sense strand and 2 nucleotides with a 2'-fluoro modification in the antisense strand.

[0410] In other embodiments, an RNAi agent of the invention may contain an ultra-low number of nucleotides containing a 2'-fluoro modification, e.g., 2 or fewer nucleotides containing a 2'-fluoro modification. For example, the RNAi agent may contain 2, 1 of 0 nucleotides with a 2'-fluoro modification. In a specific embodiment, the RNAi agent may contain 2 nucleotides with a 2'-fluoro modification, e.g., 0 nucleotides with a 2-fluoro modification in the sense strand and 2 nucleotides with a 2'-fluoro modification in the antisense strand.

[0411] Various publications describe multimeric RNAi agents that can be used in the methods of tire invention. Such publications include W02007 / 091269, US Patent No. 7858769, W02010 / 141511, W02007 / 117686, W02009 / 014887 and WO2011 / 031520 the entire contents of each of which are hereby incorporated herein by reference.

[0412] In certain embodiments, the compositions and methods of the disclosure include a vinyl phosphonate (VP) modification of an RNAi agent as described herein. In exemplary embodiments, a vinyl phosphonate of the disclosure has the following structure:

[0413] For example, when the phosphate mimic is a 5 '-vinyl phosphonate (VP), the 5 '-terminal nucleotide can have the following structure, wherein * indicates the location of the bond to 5'-position of tire adjacent nucleotide;

[0414] R is hydrogen, hydroxy, methoxy, fluoro (e.g., hydroxy or methoxy), or another modification described herein; and

[0415] B is a nucleobase or a modified nucleobase, optionally where B is adenine, guanine, cytosine, thymine or uracil. A vinyl phosphonate of the instant disclosure may be attached to either the antisense or the sense strand of a dsRNA of the disclosure. In certain embodiments, a vinyl phosphonate of the instant disclosure is attached to the antisense strand of a dsRNA, optionally at the 5' end of the antisense strand of tire dsRNA. The dsRNA agent can comprise a phosphorus-containing group at the 5 '-end of the sense strand or antisense strand. The 5'-end phosphorus-containing group can be 5'-end phosphate (5'-P), 5'- end phosphorothioate (5 '-PS). 5'-end phosphorodithioate (5'-PS2), 5'-end vinylphosphonate (5'-VP). 5'- end methylphosphonate (MePhos), or 5'-deoxy-5'-C-malonyl. When the 5 '-end phosphorus-containing group is 5 '-end vinylphosphonate (5 '-VP), the 5 '-VP can be either 5'-E-VP isomer (i.e., transvinylphosphonate , 5'-Z-VP isomer (i.e., cis-vinylphosphonate, or mixtures thereof.

[0416] Vinyl phosphate modifications are also contemplated for the compositions and methods of the instant disclosure. An exemplary' vinyl phosphate structure is:

[0417] For example, when the phosphate mimic is a 5 '-vinyl phosphate, the 5 '-terminal nucleotide can have the immediately structure, where the phosphonate group is replaced by a phosphate.

[0418] As described in more detail below, the RNAi agent that contains conjugations of one or more carbohydrate moieties to a RNAi agent can optimize one or more properties of the RNAi agent. In many cases, the carbohydrate moiety will be attached to a modified subunit of the RNAi agent. For example, the ribose sugar of one or more ribonucleotide subunits of a dsRNA agent can be replaced with another moiety, e.g., a non-carbohydrate (preferably cyclic) carrier to which is attached a carbohydrate ligand. A ribonucleotide subunit in which the ribose sugar of the subunit has been so replaced is referred to herein as a ribose replacement modification subunit (RRMS). A cyclic carrier may be a carbocyclic ring system, i.e.. all ring atoms are carbon atoms, or a heterocyclic ring system, i. e. , one or more ring atoms may be a heteroatom. e.g., nitrogen, oxygen, sulfur. The cyclic carrier may be a monocyclic ring system, or may contain two or more rings, e.g. fused rings. The cyclic carrier may be a frilly saturated ring system, or it may contain one or more double bonds.

[0419] Tire ligand may be attached to tire polynucleotide via a carrier. Tire carriers include (i) at least one "backbone attachment point,” preferably two “backbone attachment points” and (ii) at least one “tethering attachment point.” A “backbone attachment point” as used herein refers to a functional group, e.g. a hydroxyl group, or generally, a bond available for, and that is suitable for incorporation of the carrier into the backbone, e.g., the phosphate, or modified phosphate, e.g., sulfur containing, backbone, of a ribonucleic acid. A “tethering attachment point” (TAP) in some embodiments refers to a constituent ring atom of the cyclic carrier, e.g., a carbon atom or a heteroatom (distinct from an atom which provides a backbone attachment point), that connects a selected moiety. The moiety can be, e.g.. a carbohydrate, e.g. monosaccharide, disaccharide, trisaccharide, tetrasaccharide, oligosaccharide and polysaccharide. Optionally, the selected moiety is connected by an intervening tether to the cyclic carrier. Thus, the cyclic carrier will often include a functional group, e.g., an amino group, or generally, provide a bond, that is suitable for incorporation or tethering of another chemical entity, e.g., a ligand to the constituent ring.

[0420] The RNAi agents may be conjugated to a ligand via a carrier, wherein the carrier can be cyclic group or acyclic group; preferably, the cyclic group is selected from pyrrolidinyl, pyrazolinyl, pyrazolidinyl. imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl. [l,3]dioxolane. oxazolidinyl. isoxazolidinyl. morpholinyl, thiazolidinyl, isothiazolidinyl, quinoxalinyl, pyridazinonyl, tetrahydrofuryl and decalin; preferably, the acyclic group is selected from serinol backbone or diethanolamine backbone.

[0421] In another embodiment of tire invention, an iRNA agent comprises a sense strand and an antisense strand, each strand having 14 to 40 nucleotides. The RNAi agent may be represented by formula (L):

[0422] (L),

[0423] In formula (L), Bl, B2, B3, Bl', B2'. B3', and B4' each are independently a nucleotide containing a modification selected from the group consisting of 2'-O-alkyl, 2'-substituted alkoxy, 2'- substituted alkyl, 2'-halo, ENA, and BNA / LNA. In certain embodiments, Bl, B2, B3, Bl', B2', B3', and B4' each contain 2'-OMe modifications. In certain embodiments, Bl, B2, B3, Bl', B2', B3', and B4' each contain 2'-OMe or 2'-F modifications. In certain embodiments, at least one of Bl. B2, B3, Bl', B2'. B3', and B4' contain 2'-O-N-methylacetamido (2'-0-NMA) modification. C 1 is a thermally destabilizing nucleotide placed at a site opposite to the seed region of the antisense strand (i.e., at positions 2-8 of the 5'-end of the antisense strand). For example, Cl is at a position of the sense strand that pairs with a nucleotide at positions 2-8 of the 5 '-end of the antisense strand. In one example, Cl is at position 15 from the 5'-end of the sense strand. Cl nucleotide bears the thermally destabilizing modification which can include abasic modification; mismatch with the opposing nucleotide in the duplex; and sugar modification such as 2'-deoxy modification or acyclic nucleotide e.g.. unlocked nucleic acids (UNA) or glycerol nucleic acid (GNA). In certain embodiments. Cl has thermally destabilizing modification selected from tire group consisting of: i) mismatch with the opposing nucleotide in the antisense strand; ii) abasic modification selected from the group consisting of: modification selected from the group consisting of: , wherein B is a modified or unmodified nucleobase, R1and R2independently are H, halogen, OR3, or alkyl; and R3 is H, alkyl, cycloalkyl, aryl, aralkyl, heteroaryl or sugar. In certain embodiments, the thermally destabilizing modification in C 1 is a mismatch selected from the group consisting of G:G. G:A. G:U, G:T, A:A. A:C. C:C, C:U, C:T. U:U, T:T. and U:T; and optionally, at least one nucleobase in the mismatch pair is a 2'-deoxy nucleobase. In one example, the thermally destabilizing modification in Cl is GNA or

[0424] Tl, IT, T2', and T3' each independently represent a nucleotide comprising a modification providing the nucleotide a steric bulk that is less or equal to the steric bulk of a 2'-0Me modification. A steric bulk refers to the sum of steric effects of a modification. Methods for determining steric effects of a modification of a nucleotide are known to one skilled in the art. The modification can be at the 2' position of a ribose sugar of the nucleotide, or a modification to a non-ribose nucleotide, acyclic nucleotide, or the backbone of the nucleotide that is similar or equivalent to the 2' position of the ribose sugar, and provides the nucleotide a steric bulk that is less than or equal to the steric bulk of a 2'-0Me modification. For example, Tl, Tl', T2', and T3' are each independently selected from DNA, RNA, LNA, 2'-F, and 2'-F-5'-methyl. In certain embodiments, Tl is DNA. In certain embodiments, Tl' is DNA, RNA or LNA. In certain embodiments, T2' is DNA or RNA. In certain embodiments, T3' is DNA or RNA. n1, n3, and q1are independently 4 to 15 nucleotides in length. n5, q3, and q7are independently 1-6 nucleotide(s) in length. n4, q2. and qsare independently 1-3 nucleotide(s) in length; alternatively, n4is 0. q5is independently 0-10 nucleotide(s) in length. n2and q4are independently 0-3 nucleotide(s) in length.

[0425] Alternatively, n4is 0-3 nucleotide(s) in length.

[0426] In certain embodiments, n4can be 0. In one example, n4is 0, and q2and q6are 1. In another example, n4is 0. and q2and q6are 1, with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5'-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'- end of the antisense strand).

[0427] In certain embodiments, n4, q2, and q6are each 1.

[0428] In certain embodiments, n2, n4, q2. q4, and qbare each 1.

[0429] In certain embodiments. Cl is at position 14-17 of tire 5 '-end of the sense strand, when the sense strand is 19-22 nucleotides in length, and n4is 1 . In certain embodiments, Cl is at position 15 of the 5'- end of the sense strand

[0430] In certain embodiments, T3' starts at position 2 from the 5' end of the antisense strand. In one example, T3' is at position 2 from the 5' end of tire antisense strand and qbis equal to 1.

[0431] In certain embodiments. Tl' starts at position 14 from the 5' end of the antisense strand. In one example, Tl ' is at position 14 from the 5 ' end of tire antisense strand and q2is equal to 1.

[0432] In an exemplary embodiment, T3' starts from position 2 from the 5' end of the antisense strand and Tl' starts from position 14 from the 5' end of the antisense strand. In one example, T3' starts from position 2 from the 5' end of the antisense strand and q6is equal to 1 and Tl' starts from position 14 from the 5 ' end of the antisense strand and q2is equal to 1. In certain embodiments, IT and T3' are separated by 11 nucleotides in length (i.e. not counting the IT and T3' nucleotides).

[0433] In certain embodiments, IT is at position 14 from the 5' end of the antisense strand. In one example, IT is at position 14 from the 5' end of the antisense strand and q2is equal to 1, and the modification at the 2' position or positions in a non-ribose, acyclic or backbone that provide less steric bulk than a 2'-0Me ribose.

[0434] In certain embodiments, T3' is at position 2 from the 5' end of the antisense strand. In one example, T3' is at position 2 from the 5' end of the antisense strand and q6is equal to 1, and tire modification at the 2' position or positions in a non-ribose, acyclic or backbone that provide less than or equal to steric bulk than a 2'-0Me ribose.

[0435] In certain embodiments. T1 is at the cleavage site of the sense strand. In one example, T1 is at position 11 from the 5' end of the sense strand, when the sense strand is 19-22 nucleotides in length, and n2is I . In an exemplary embodiment, T1 is at the cleavage site of the sense strand at position 11 from the 5' end of the sense strand, when the sense strand is 19-22 nucleotides in length, and n2is 1,

[0436] In certain embodiments, T2' starts at position 6 from the 5' end of the antisense strand. In one example, T2' is at positions 6-10 from the 5' end of the antisense strand, and q4is 1.

[0437] In an exemplary embodiment, T1 is at the cleavage site of the sense strand, for instance, at position 11 from the 5' end of the sense strand, when the sense strand is 19-22 nucleotides in length, and n2is 1 ; T1 ' is at position 14 from the 5' end of tire antisense strand, and q2is equal to 1, and the modification to IT is at the 2' position of a ribose sugar or at positions in a non-ribose, acyclic or backbone that provide less steric bulk than a 2'-OMe ribose; T2' is at positions 6-10 from the 5' end of the antisense strand, and q4is 1 ; and T3 ' is at position 2 from the 5 ' end of the antisense strand, and q6is equal to 1. and the modification to T3' is at the 2' position or at positions in a non-ribose, acyclic or backbone that provide less than or equal to steric bulk than a 2'-OMe ribose.

[0438] In certain embodiments, T2' starts at position 8 from the 5' end of the antisense strand. In one example, T2' starts at position 8 from the 5' end of the antisense strand, and q4is 2.

[0439] In certain embodiments, T2' starts at position 9 from the 5' end of the antisense strand. In one example, T2' is at position 9 from the 5" end of tire antisense strand, and q4is 1.

[0440] In certain embodiments. Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'- F. q3is 4, T2' is 2'-F, q4is 1, B3' is 2'-0Me or 2'-F, q5is 6. T3' is 2'-F. q6is 1. B4' is 2'-OMe. and q7is 1; with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5‘-end of the antisense strand). In certain embodiments, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1 , B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 1, B3' is 2'-OMe or 2'-F, q5is 6, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand).

[0441] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2‘OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-0Me or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1.

[0442] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q3is 5, T3' is 2'-F, q” is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end of the antisense strand).

[0443] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 6, T1 is 2'F, n2is 3, B2 is 2'-OMe. n3is 7, n4is 0, B3 is 2'OMe, n3is 3, Bl' is 2'-OMe or 2'-F, q1is 7, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1.

[0444] In certain embodiments, Bl is 2'-OMe or 2 -F, n1is 6, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 7, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of tire antisense strand (counting from the 5‘-end of the antisense strand).

[0445] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'OMe. n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F. q4is 1, B3' is 2'-OMe or 2'-F, q5is 6, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1.

[0446] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 1, B3' is 2'-OMc or 2'-F, q5is 6, T3' is 2'-F, q6is 1, B4' is 2'-OMc, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end of the antisense strand).

[0447] In certain embodiments, Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n ' is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-0Me or 2'-F, q3is 5, T2' is 2'-F, q4is 1, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1; optionally with at least 2 additional TT at the 3 '-end of the antisense strand.

[0448] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 5, T2' is 2'-F, q4is 1, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; optionally with at least 2 additional TT at the 3 '-end of the antisense strand; with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand).

[0449] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is

[0450] 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-OMe. and q7is 1.

[0451] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe. n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within positions 1-5 of the sense strand (counting from the 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end).

[0452] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-0Me or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1.

[0453] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F. q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2 -F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within positions 1 -5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me. n3is 7. n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1.

[0454] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1. B4' is 2'-F. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within positions 1 -5 of the sense strand (counting from the 5'-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand).

[0455] The RNAi agent can comprise a phosphorus-containing group at the 5'-end of the sense strand or antisense strand. The 5'-end phosphorus-containing group can be 5'-end phosphate (5'-P), 5'-end phosphorothioate (5'-PS), 5'-end phosphorodithioate ( 5'-PS2). 5'-end vinylphosphonate (5'-VP), 5'-end m ethylphosph onate (Me Phos), or 5' -deoxy-5' -C-malonyl . When the 5 '-end phosphorus-containing group is 5'-end vinylphosphonate (5'-VP), the 5'-VP can be either 5'-E-VP isomer (i.e., trans -vinylphosphonate, . 5 -Z-VP isomer (i.e., cis-vinylphosphonate. or mixtures thereof.

[0456] In certain embodiments, the RNAi agent comprises a phosphorus-containing group at the 5 '-end of the sense strand. In certain embodiments, the RNAi agent comprises a phosphorus-containing group at the 5 '-end of the antisense strand.

[0457] In certain embodiments, the RNAi agent comprises a 5'-P. In certain embodiments, the RNAi agent comprises a 5'-P in the antisense strand.

[0458] In certain embodiments, the RNAi agent comprises a 5'-PS. In certain embodiments, the RNAi agent comprises a 5 '-PS in the antisense strand.

[0459] In certain embodiments, the RNAi agent comprises a 5 '-VP. In certain embodiments, the RNAi agent comprises a 5 ‘-VP in the antisense strand, hi certain embodiments, the RNAi agent comprises a 5'- E-\'P in the antisense strand. In certain embodiments, the RNAi agent comprises a 5'-Z-VP in the antisense strand.

[0460] In certain embodiments, tire RNAi agent comprises a 5 '-PS2. In certain embodiments, the RNAi agent comprises a 5 -PS2in the antisense strand.

[0461] In certain embodiments, the RNAi agent comprises a 5 -PS2. In certain embodiments, the RNAi agent comprises a 5'-deoxy-5'-C-malonyl in tire antisense strand.

[0462] In certain embodiments, Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n' is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5 '-PS.

[0463] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'OMe. n5is 3, Bl' is 2 -OMe or 2 -F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5'-P.

[0464] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1. The RNAi agent also comprises a 5 -VP. The 5'-VP may be 5 -E-VP. 5'-Z-VP. or combination thereof.

[0465] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5'- PS2.

[0466] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'OMe. n5is 3. Bl' is 2'-OMe or 2 -F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2 -F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl.

[0467] In certain embodiments, Bl is 2'-OMe or 2 -F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of tire antisense strand (counting from tire 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-P. In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of tire sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-PS.

[0468] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2‘ is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of tire antisense strand (counting from the 5 ‘-end of the antisense strand). Tire RNAi agent also comprises a 5'-VP. Tire 5'-VP may be 5 -E-VP, 5 -Z-VP, or combination thereof.

[0469] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q' is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q” is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of tire sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 ‘-end of the antisense strand). The RNAi agent also comprises a 5'- PS2.

[0470] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl.

[0471] In certain embodiments, Bl is 2'-OMc or 2 -F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMc, n3is 7, n4is 0, B3 is 2'-OMe, nsis 3, Bl' is 2'-0Me or 2'-F. q1is 9, T1‘ is 2'-F, q2is 1, B2‘ is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 1, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5'-P.

[0472] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n ' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2 -F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The dsRNA agent also comprises a 5'-PS.

[0473] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5'-VP. The 5'-VP may be 5 -.E-VP, 5'-Z-VP, or combination thereof.

[0474] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q' is 7, T3' is 2'-F, q” is 1, B4' is 2'-OMe, and q7is 1. The RNAi agent also comprises a 5'- PS2.

[0475] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-OMe. and q7is 1. The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl.

[0476] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5 -P.

[0477] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5'-PS.

[0478] In certain embodiments, Bl is 2'-OMc or 2 -F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMc, n3is 7, n4is 0, B3 is 2'-OMe, nsis 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2‘ is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). Tire RNAi agent also comprises a 5 -VP. The 5'-VP may be 5'-E-VP, 5'-Z- VP, or combination thereof.

[0479] In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me. n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q" is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications w ithin position 1-5 of the sense strand (counting from the 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5'- PS2.

[0480] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl.

[0481] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n ' is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-0Me or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1. Tire RNAi agent also comprises a 5'- P.

[0482] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe. n3is 7, n4is 0, B3 is 2'OMe, IT is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1. The RNAi agent also comprises a 5'- PS.

[0483] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'OMe. n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F. q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2 -F, and q7is 1. The RNAi agent also comprises a 5'- VP. The 5 '-VP may be 5'-E-VP, 5'-Z-VP, or combination thereof.

[0484] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'OMc, n5is 3, Bl' is 2'-OMc or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-0Mc or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1. The dsRNA RNA agent also comprises a 5'- PS2. In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n' is 7, n4is 0, B3 is 2'OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1. The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl.

[0485] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q ' is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). Tire RNAi agent also comprises a 5'- P.

[0486] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS.

[0487] In certain embodiments, Bl is 2'-OMe or 2 -F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-F, and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- VP. The 5 '-VP may be 5'-E-VP, 5'-Z-VP, or combination thereof.

[0488] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q" is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS2.

[0489] In certain embodiments, Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n ' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-F, and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5 ' -deoxy-5 ' -C-malonyl .

[0490] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q3is 7, T3' is 2'-F, q” is 1, B4' is 2'-F, and q7is 1. The RNAi agent also comprises a 5'- P.

[0491] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-F. and q7is 1. The RNAi agent also comprises a 5'- PS.

[0492] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4‘ is 2'-F, and q7is 1. The RNAi agent also comprises a 5'- VP. Tire 5 '-VP may be 5 -Ti-VP, 5 -Z-VP, or combination thereof.

[0493] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q' is 4, q4is 0, B3' is 2'-OMe or 2'-F, q3is 7, T3' is 2'-F, q” is 1, B4' is 2'-F, and q7is 1. The RNAi agent also comprises a 5'- PS2.

[0494] In certain embodiments, Bl is 2'-OMe or 2 -F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-F. and q7is 1. The RNAi agent also comprises a 5 '-deoxy-5 '-C-malonyl.

[0495] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMc or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4‘ is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- P.

[0496] In certain embodiments, Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1. B4' is 2'-F. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5'-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of tire antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS.

[0497] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe. n3is 7, n4is 0, B3 is 2'-0Me, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q" is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- VP. The 5 '-VP may be 5'-E-VP, 5'-Z-VP, or combination thereof.

[0498] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n ' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4‘ is 2'-F. and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS2.

[0499] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2 -F, q6is 1. B4' is 2'-F. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5 ' -deoxy- 5 ' -C-malonyl . In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of tire sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-P and a targeting ligand. In certain embodiments, the 5'-P is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0500] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-PS and atargeting ligand. In certain embodiments, the 5'-PS is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0501] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-VP (e.g., a 5'-E-VP, 5'-Z-VP, or combination thereof), and atargeting ligand.

[0502] In certain embodiments, the 5 '-VP is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0503] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9. Tl' is 2'-F. q2is 1. B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q" is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of tire sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS2 and a targeting ligand. In certain embodiments, the 5'-PS2 is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0504] In certain embodiments, Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n ' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2‘ is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2'-OMe. and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from tire 5 ‘-end of the antisense strand). The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl and a targeting ligand. In certain embodiments, the 5'- deoxy-5'-C-malonyl is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0505] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4‘ is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5 -P and a targeting ligand. In certain embodiments, the 5'-P is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0506] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2 -F, q6is 1. B4' is 2'-OMe. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications w ithin positions 18-23 of the antisense strand (counting from tire 5'-end). The RNAi agent also comprises a 5 -PS and a targeting ligand. In certain embodiments, the 5 '-PS is at tire 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0507] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMc or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4‘ is 2'-OMc, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5'-VP (e g., a 5'-£-VP, 5'-Z-VP, or combination thereof) and a targeting ligand. In certain embodiments, the 5'-VP is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0508] In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q ' is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications w ithin positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5 -PS2 and a targeting ligand. In certain embodiments, the 5'-PS2 is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0509] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n ' is 7, n4is 0, B3 is 2‘-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-OMe, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5'-end). The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl and atargeting ligand. In certain embodiments, the 5'-deoxy-5'-C-malonyl is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0510] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q' is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q3is 5, T3' is 2'-F, q” is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). Tire RNAi agent also comprises a 5 -P and a targeting ligand. In certain embodiments, tire 5'-P is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0511] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMc, n5is 3, Bl' is 2'-0Mc or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMc or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, qsis 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1 ; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-PS and a targeting ligand. In certain embodiments, the 5 -PS is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0512] In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me. n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-VP (e.g., a 5'-E-VP, 5'-Z-VP, or combination thereof) and a targeting ligand. In certain embodiments, the 5 '-VP is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0513] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F. q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1. B4' is 2 -F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-PS2 and a targeting ligand. In certain embodiments, the 5'-PS2 is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0514] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, T2' is 2'-F, q4is 2, B3' is 2'-OMe or 2'-F, q5is 5, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl and a targeting ligand. In certain embodiments, the 5'-deoxy-5'-C-malonyl is at the 5'-cnd of the antisense strand, and the targeting ligand is at the 3'-cnd of the sense strand.

[0515] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q' is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 1, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). Tire RNAi agent also comprises a 5'-P and a targeting ligand. In certain embodiments, tire 5'-P is at the 5'-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0516] In certain embodiments, Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2‘-OMe, n5is 3, Bl' is 2'-0Me or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4‘ is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS and a targeting ligand. In certain embodiments, the 5'-PS is at the 5'-end of the antisense strand, and tire targeting ligand is at the 3 '-end of the sense strand.

[0517] In certain embodiments. Bl is 2'-OMe or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0. B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9. Tl' is 2'-F. q2is 1, B2' is 2'-OMe or 2'-F, q' is 4, q4is 0, B3' is 2'-OMe or 2'-F, q3is 7, T3' is 2'-F, q” is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of tire sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). Tire RNAi agent also comprises a 5'- VP (e.g.. a 5'-E-VP, 5'-Z-VP, or combination thereof) and a targeting ligand. In certain embodiments, the 5 '-VP is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of the sense strand.

[0518] In certain embodiments, Bl is 2'-OMe or 2 -F, n1is 8, Tl is 2'F, n2is 3, B2 is 2'-OMe, n3is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-0Me or 2'-F. q1is 9, Tl' is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7. T3' is 2'-F, q6is 1, B4' is 2'-F. and q7is 1: with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from the 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'- PS2 and a targeting ligand. In certain embodiments, the 5'-PS2 is at tire 5 '-end of the antisense strand, and tire targeting ligand is at the 3 '-end of the sense strand. In certain embodiments. Bl is 2'-0Me or 2'-F, n1is 8, T1 is 2'F, n2is 3, B2 is 2'-0Me, n' is 7, n4is 0, B3 is 2'-OMe, n5is 3, Bl' is 2'-OMe or 2'-F, q1is 9, IT is 2'-F, q2is 1, B2' is 2'-OMe or 2'-F, q3is 4, q4is 0, B3' is 2'-OMe or 2'-F, q5is 7, T3' is 2'-F, q6is 1, B4' is 2'-F, and q7is 1; with two phosphorothioate intemucleotide linkage modifications within position 1-5 of the sense strand (counting from tire 5 '-end of the sense strand), and two phosphorothioate intemucleotide linkage modifications at positions 1 and 2 and two phosphorothioate intemucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5 '-end of the antisense strand). The RNAi agent also comprises a 5'-deoxy-5'-C-malonyl and a targeting ligand. In certain embodiments, the 5'-deoxy-5'-C-malonyl is at the 5 '-end of the antisense strand, and the targeting ligand is at the 3 '-end of tire sense strand.

[0519] In a particular embodiment, an RNAi agent of the present invention comprises:

[0520] (a) a sense strand having:

[0521] (i) a length of 21 nucleotides;

[0522] (ii) an ASGPR ligand attached to the 3 '-end, wherein said ASGPR ligand comprises three GalNAc derivatives attached through a trivalent branched linker; and

[0523] (iii) 2'-F modifications at positions 1, 3, 5, 7, 9 to 11, 13, 17, 19, and 21, and 2'-0Me modifications at positions 2, 4, 6, 8, 12, 14 to 16, 18, and 20 (counting from the 5' end); and

[0524] (b) an antisense strand having:

[0525] (i) a length of 23 nucleotides:

[0526] (ii) 2'-0Me modifications at positions 1, 3, 5, 9, 11 to 13, 15, 17, 19, 21, and 23, and 2'F modifications at positions 2, 4, 6 to 8, 10, 14, 16, 18, 20, and 22 (counting from the 5' end); and

[0527] (iii) phosphorothioate intemucleotide linkages between nucleotide positions 21 and 22, and between nucleotide positions 22 and 23 (counting from the 5' end): wherein the dsRNA agents have a two-nucleotide overhang at the 3 '-end of the antisense strand, and a blunt end at the 5 '-end of the antisense strand.

[0528] In another particular embodiment, an RNAi agent of the present invention comprises:

[0529] (a) a sense strand having:

[0530] (i) a length of 21 nucleotides;

[0531] (ii) an ASGPR ligand attached to the 3 '-end, wherein said ASGPR ligand comprises three GalNAc derivatives attached through a trivalent branched linker;

[0532] (iii) 2'-F modifications at positions 1, 3, 5, 7, 9 to 11, 13, 15, 17, 19, and 21, and 2'-0Me modifications at positions 2, 4, 6, 8, 12, 14, 16, 18, and 20 (counting from the 5' end); and (iv) phosphorothioate intemucleotide linkages between nucleotide positions 1 and 2, and between nucleotide positions 2 and 3 (counting from the 5' end); and

[0533] (b) an antisense strand having:

[0534] (i) a length of 23 nucleotides;

[0535] (ii) 2'-0Me modifications at positions 1, 3. 5, 7, 9, 11 to 13, 15, 17, 19, and 21 to 23. and 2'F modifications at positions 2, 4, 6, 8, 10, 14, 16, 18, and 20 (counting from the 5' end); and

[0536] (iii) phosphorothioate intemucleotide linkages between nucleotide positions 1 and 2, between nucleotide positions 2 and 3, between nucleotide positions 21 and 22, and between nucleotide positions 22 and 23 (counting from the 5‘ end); wherein the RNAi agents have a two-nucleotide overhang at the 3 '-end of the antisense strand, and a blunt end ...

Claims

We Claim:

1. A double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of Aminoadipatesemialdehyde synthase (AASS) in a cell, wherein said dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein said antisense strand comprises a region of complementarity to an mRNA encoding AASS which comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the antisense sequences listed in any one of Tables 3-6.

2. Tire dsRNA agent of claim 1, wherein said dsRNA agent comprises at least one modified nucleotide.

3. Tire dsRNA agent of claim 1 or 2, wherein substantially all of the nucleotides of the sense strand comprise a modification.

4. Tire dsRNA agent of claim 1 or 2. wherein substantially all of the nucleotides of the antisense strand comprise a modification.

5. The dsRNA agent of claim 1 or 2. wherein substantially all of the nucleotides of the sense strand and substantially all of the nucleotides of the antisense strand comprise a modification.

6. A double stranded RNA (dsRNA) agent for inhibiting expression of Aminoadipatesemialdehyde synthase (AASS) in a cell, wherein the double stranded RNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the sense sequences listed in any one of Tables 3-6 and the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the antisense sequences listed in any one of Tables 3-6, wherein substantially all of the nucleotides of the sense strand and substantially all of the nucleotides of the antisense strand are modified nucleotides, and wherein the sense strand is conjugated to a ligand attached at the 3'-terminus.

7. Tire dsRNA agent of claim 6, wherein all of the nucleotides of the sense strand comprise a modification.

8. The dsRNA agent of claim 6, wherein all of the nucleotides of the antisense strand comprise a modification.

9. The dsRNA agent of claim 6, wherein all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand comprise a modification.

10. The dsRNA agent of any one of claims 2-9. wherein at least one of said modified nucleotides is selected from the group consisting of a deoxy -nucleotide, a 3'-tenninal deoxy-thymine (dT) nucleotide, a 2'- O-methyl modified nucleotide, a 2'-fluoro modified nucleotide, a 2'-deoxy-modified nucleotide, a locked nucleotide, an unlocked nucleotide, a conformationally restricted nucleotide, a constrained ethyl nucleotide, an abasic nucleotide, a 2'-amino-modified nucleotide, a 2'-O-allyl-modified nucleotide, 2'-C-alkyl-modified nucleotide, 2 '-hydroxyl -modified nucleotide, a 2 '-methoxy ethyl modified nucleotide, a 2'-O-alkyl-modified nucleotide, a morpholino nucleotide, a phosphoramidate, a non-natural base comprising nucleotide, a tetrahydropyran modified nucleotide, a 1,5-anhydrohexitol modified nucleotide, a cyclohexenyl modified nucleotide, a nucleotide comprising a phosphorothioate group, a nucleotide comprising a methylphosphonate group, a nucleotide comprising a 5 '-phosphate, a nucleotide comprising a 5 '-phosphate mimic, a glycol modified nucleotide, and a 2-O-(N-methylacetamide) modified nucleotide, and combinations thereof.

11. Tire dsRNA agent of claim 11, wherein the nucleotide modifications are 2'-O-methyl and / or 2 '-fluoro modifications.

12. The dsRNA agent of any one of claims 1-11, wherein the region of complementarity is at least 17 nucleotides in length.

13. The dsRNA agent of any one of claims 1-12, wherein the region of complementarity is 19 to 30 nucleotides in length.

14. The dsRNA agent of claim 13, wherein the region of complementarity is 19-25 nucleotides in length.

15. Tire dsRNA agent of claim 14, wherein the region of complementarity is 21 to 23 nucleotides in length.

16. Tire dsRNA agent of any one of claims 1-15, wherein each of the sense and antisense strands is no more than 30 nucleotides in length.

17. The dsRNA agent of any one of claims 1-16, wherein each of the sense and antisense strands is independently 19-30 nucleotides in length.

18. The dsRNA agent of claim 17, wherein each of the sense and antisense strands is independently 19-25 nucleotides in length.

19. The dsRNA agent of claim 17, wherein each of the sense and antisense strands is independently 21-23 nucleotides in length.

20. The dsRNA agent of any one of claims 1-19, wherein the at least one of the sense or antisense strands comprises a 3' overhang of at least 1 nucleotide.

21. Tire dsRNA agent of any one of claim 20, wherein the at least one of the sense or antisense strands comprises a 3' overhang of at least 2 nucleotides.

22. Tire dsRNA agent of any one of claims 1-5 and 10-21 further comprising a ligand.

23. Tire dsRNA agent of claim 22, wherein the ligand is conjugated to the 3 ' end of the sense strand of the dsRNA agent.

24. The dsRNA agent of claim 6 or 23, wherein the ligand is an N-acctylgalactosaminc (GalNAc) derivative.

25. The dsRNA agent of claim 24, wherein the ligand is26. Tire dsRNA agent of claim 25, wherein the dsRNA agent is conjugated to the ligand as shown in the following schematic27. The dsRNA agent of claim 26, wherein the X is 0.

28. The dsRNA agent of claim 1, wherein the region of complementarity comprises any one of the antisense sequences in any one of Tables 3-6.

29. A double stranded ribonucleic acid (dsRNA) agent for inhibiting the expression of Aminoadipate -semialdehyde synthase (AASS) in a cell, wherein the dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the sense sequences listed in any one of Tables 3-6 and the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the sense sequences listed in any one of Tables 3-6, wherein substantially all of the nucleotides of the sense strand comprise a modification selected from the group consisting of a 2'-O-mcthyl modification and a 2'-fluoro modification, wherein the sense strand comprises two phosphorothioate intemucleotide linkages at the 5'- tenninus, wherein substantially all of the nucleotides of the antisense strand comprise a modification selected from the group consisting of a 2 '-0 -methyl modification and a 2 '-fluoro modification, wherein the antisense strand comprises two phosphorothioate intemucleotide linkages at the 5 '-terminus and two phosphorothioate intemucleotide linkages at the 3 '-terminus, and wherein the sense strand is conjugated to one or more GalNAc derivatives attached through a monovalent, bivalent or trivalent branched linker at the 3 '-terminus.

30. The dsRNA agent of claim 29, wherein all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand are modified nucleotides.

31. The dsRNA agent of claim 29 or 30, wherein the dsRNA agent comprises any one of the antisense sequences listed in any one of Tables 3-6.

32. The dsRNA agent of any one of claims 1-31, wherein the sense strand and the antisense strand comprise nucleotide sequences selected from the group consisting of the nucleotide sequences of any one of the agents listed in any one of Tables 3-6.

33. A double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of Aminoadipatesemialdehyde synthase (AASS) in a cell, wherein the dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises a nucleotide sequence of any one of the agents in any one of Tables 3-6, and the antisense strand comprises a nucleotide sequence of any one of the agents in any one of Tables 3-6, wherein substantially all of the nucleotide of the sense strand and substantially all or all of the nucleotides of tire antisense strand are modified nucleotides, and wherein the dsRNA agent is conjugated to a ligand.

34. The dsRNA agent of any one of claims 1-33, wherein the dsRNA agent is selected from tire group consisting of AD-2320882.1, AD-2320938.1, AD-2321352.

1. AD-2321573.1, AD-2321665.1, AD-2321839.1, AD-2321863.1, AD-2322178.1, AD-2322257.

1. AD-2322371.1, AD-2322980.1, AD-2323248.1, AD-2323253.1, AD-2323445.1, AD-2323482.

1. AD-2323584.1, AD-2323585.1, AD-2323784.1, AD-2323856.1, AD-2323858.1, AD-2323886.1, AD-2323961.

1. AD-2323965.1, AD-2323970.1, AD-2323972.1, AD-2323976.1, AD-2324043.

1. AD-2324044.

1. AD-2324046.1, AD-2324047.1, AD-2324276.1, AD-2324670.1, AD-2325059. 1, AD-2325148. 1, AD-2325356. 1, AD-2325357.1, AD-2325369.1, AD-2325373. 1, AD-2325448.1, AD-2325450.1, AD-2325473.1, AD-2325474.1, AD-2325477.1, AD-2325546.1, AD-2325552.1, AD-2325646.1, AD-2325648.1, AD-2325674.1, AD-2325677.1, AD-2325678.1, AD-2325679.1, AD-2325681.1, AD-2325744.1, AD-2325745.1, AD-2325746.1, AD-2325748.1, AD-2325752.1, AD-2325762.1, AD-2325763.1, AD-2325764.1, AD-2325765.1, AD-2325769.1, AD-2325780.1, AD-2325781.1, AD-2325782.1, AD-2325784.1, AD-2325785.1, AD-2325786.1, AD-2325837.1, AD-2325838.1, AD-2325839.1, AD-2325840.1, AD-2325847.1, AD-2325848.1, AD-2325955.1, AD-2325959.1, AD-2325968.1, AD-2325969.1, AD-2325973.1, AD-2325976.1, AD-2325979.1, AD-2325984.1, AD-2326042.1, AD-2326067.1, AD-2326170.1, AD-2328140.1, AD-2328186.1, AD-2328257.1, AD-2328266.1, and AD-2328843.1,35. The dsRNA of any one of claims 1-34 wherein the dsRNA agent targets a hotspot region of air mRNA encoding AASS.

36. A dsRNA agent that targets a hotspot region of a Aminoadipate-semialdehyde synthase (AASS) mRNA.

37. A cell containing the dsRNA agent of any one of claims 1-36.

38. A vector encoding at least one of the sense or antisense strands of the dsRNA agent of any one of claims 1-36.

39. A pharmaceutical composition for inhibiting expression of the Aminoadipate-semialdehyde synthase (AASS) gene comprising the dsRNA agent of any one of claims 1-36.

40. Tire pharmacal composition of claim 39, wherein the agent is formulated in an unbuffered solution.

41. The pharmaceutical composition of claim 40, wherein the unbuffered solution is saline or water.

42. The pharmaceutical composition of claim 39, wherein the agent is fonnulated with a buffered solution.

43. The phamraceutical composition of claim 42, wherein said buffered solution comprises acetate, citrate, prolamine, carbonate, or phosphate or any combination thereof.

44. Tire pharmaceutical composition of claim 42, wherein the buffered solution is phosphate buffered saline (PBS).

45. A method of inhibiting Aminoadipate-semialdehyde synthase (AASS) expression in a cell, the method comprising contacting the cell with the agent of any one of claims 1-36, or a pharmacal composition of any one of claims 39-44, thereby inhibiting expression of AASS in the cell.

46. Tire method of claim 45, wherein said cell is within a subject.

47. The method of claim 46, wherein the subject is a human.

48. The method of any one of claims 45-47, wherein the AASS expression is inhibited by at least 30%, 40%, 50%, 60%, 70%, 80%. 90%. 95%, or to below the level of detection of AASS expression.

49. The method of claim 48, wherein the human subject suffers from an AASS-associated disease, disorder, or condition.

50. The method of claim 49, wherein the AASS-associated disease, disorder, or condition is a lysine catabolism disorder.

51. Tire method of claim 50, wherein the lysine catabolism disorder is glutaric aciduria type 1 (GAI).

52. Tire method of claim 50, wherein the lysine catabolism disorder is pyridoxine-dependent epilepsy (PDE).

53. A method of inhibiting the expression of AASS in a subject, the method comprising administering to the subject a therapeutically effective amount of the dsRNA agent of any one of claims 1-36, or a pharmaceutical composition of any one of claims 39-44, thereby inhibiting the expression of AASS in said subject.

54. A method of treating a subject suffering from an AASS-associated disease, disorder, or condition, comprising administering to the subject a therapeutically effective amount of the agent of any one of claims 1-36, or a pharmaceutical composition of any one of claims 39-44, thereby treating the subject suffering from an AASS-associated disease, disorder, or condition.

55. A method of preventing at least one symptom in a subject having a disease, disorder or condition that would benefit from reduction in expression of an AASS gene, comprising administering to the subject a prophylactically effective amount of the agent of any one of claims 1-36, or a pharmaceutical composition of any one of claims 39-44, thereby preventing at least one symptom in a subject having a disease, disorder or condition that would benefit from reduction in expression of an AASS gene.

56. The method of any one of claims 53-55, wherein the AASS-associated disease, disorder, or condition is a lysine catabolism disorder.

57. The method of claim 56, wherein the lysine catabolism disorder is glutaric aciduria type 1 (GAI).

58. The method of claim 57, wherein the lysine catabolism disorder is pyridoxine-dependent epilepsy (PDE).

59. The method of any one of claims 46-58, further comprising administering an additional therapeutic to the subject.

60. Tire method of any one of claims 46-59, wherein the dsRNA agent is administered to the subject at a dose of about 0.01 mg / kg to about 10 mg / kg or about 0.5 mg / kg to about 50 mg / kg.

61. Tire method of any one of claims 46-60, wherein the agent is administered to the subject intravenously, intramuscularly, or subcutaneously.

62. Tire method of any one of claims 46-61, further comprising determining the level of AASS in the subject.

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