Compounds, methods and pharmaceutical compositions for modulating DUX4 expression

Abstract

The purpose of the present invention is to provide a compound, a method, and a pharmaceutical composition for normalizing DUX4 of an individual having abnormal expression of double homeobox 4 (DUX4) gene. Provided is a modified oligonucleotide comprising 12 to 30 residues and including at least an eight contiguous nucleobase sequence that is complementary to an equal length portion in, from the 5' end, positions 126-147, 232-248, 1306-1325 or 1472-1495 of the nucleic acid bases of mature mRNA of DUX4 of SEQ ID NO: 1. The nucleic acid bases sequence of the modified oligonucleotide is at least 90% complementary to the equal length portion of the nucleic acid base sequence of mature mRNA of DUX4 of SEQ ID NO: 1.

Description

[Technical field]

[0001] The present invention relates to compounds, methods of using the compounds, and pharmaceutical compositions containing the compounds for reducing the expression of DUX4 mRNA and protein in animals. The methods of the present invention are useful for treating, preventing, or alleviating DUX4-related diseases, such as facioscapulohumeral muscular dystrophy (FSHD). [Background technology]

[0002] Facioscapulohumeral muscular dystrophy (FSHD) is a muscular dystrophy that occurs at an estimated frequency of 1 in 20,000 worldwide and 1 in 7,500 in Europe. It is the third most common muscular dystrophy after Duchenne muscular dystrophy and myotonic dystrophy. The initial symptom is muscle weakness in the face, upper limbs, scapular region, and upper limb girdle, and as the disease progresses, the lower limb girdle and lower limbs are also affected. In approximately 20% of cases, the patient is wheelchair bound by the age of 40 (even in middle age, there are cases where only mild facial muscle involvement is observed). Pain, nerve hearing loss, and retinopathy are also common. Approximately 90% of patients develop the disease by the age of 20. Severe patients (approximately 4%) show muscle weakness from infancy.

[0003] FSHD is classified into two types, FSHD1 and FSHD2, depending on the causative gene. FSHD1 type accounts for approximately 95% of all FSHD patients. In FSHD1 type patients, the D4Z4 repeat region of 4q35 is genetically shortened (1 to 10 D4Z4 repeats), which causes abnormal expression of DUX4 encoded in the D4Z4 repeat region (DUX4 is not expressed in healthy individuals). FSHD2 type accounts for approximately 5% of all FSHD patients, and abnormal expression of DUX4 occurs due to SMCHD1 (DNA methyltransferase) mutations. DUX4 has a transcription factor-like function and expresses a group of genes that cause apoptosis and muscle atrophy of muscle cells encoded downstream. Abnormal expression of DUX4 is due to possession of an allele called 4qA out of two alleles, 4qA and 4qB. The polyadenylation site present in 4qA is necessary for stabilization of DUX4 mRNA (Non-Patent Document 1, Non-Patent Document 2, Non-Patent Document 3).

[0004] Antisense technology is emerging as an effective means for regulating the expression of certain gene products and may therefore prove uniquely useful in a number of therapeutic, diagnostic, and research applications for modulating DUX4.

[0005] A method for suppressing expression of the DUX4 gene using an adeno-associated virus encoding DUX4 miRNA has been reported (Patent Document 1). However, preparing the adeno-associated virus is complicated, and it is difficult to deliver it to the required muscles throughout the body.

[0006] A method of suppressing the expression of the DUX4 gene using a lentivirus encoding DUX4 shRNA has been reported (Non-Patent Document 2), but the preparation of the lentivirus is complicated, and it is difficult to deliver it to the required muscles throughout the body. Furthermore, the residual activity of the gene suppression in quadriceps and trapezius muscle cells in vitro is 21% and 44%, respectively, which is not sufficient.

[0007] A compound in which multiple antisense oligonucleotides against DUX4 are linked has been reported (Patent Document 2), but it is not a modified oligonucleotide and its inhibitory effect is not sufficient.

[0008] Antisense oligonucleotide compounds that bind to the splicing site of DUX4 mRNA have been reported (Patent Document 3). However, these compounds are selective for pre-mRNA containing introns, and therefore have a weak inhibitory effect on mature mRNA. In addition, because knockdown is achieved by Lipofection, it is difficult to administer these compounds to the body.

[0009] Current FSHD treatment methods include symptomatic rehabilitation (stretching and exercise), administration of NSAIDs, respiratory care, etc., but these methods are ineffective and impose a heavy burden on patients. Therefore, it is an object of the present invention to provide compounds, compositions and methods for treating FSHD. [Prior art documents] [Patent documents]

[0010] [Patent Document 1] International Publication No. 2013 / 016352 [Patent Document 2] International Publication No. 2017 / 007886 [Patent Document 3] US Publication No. 2012 / 0225034 [Non-patent literature]

[0011] [Non-Patent Document 1] Snider et al.,PLoS 2010,Vol.6(10) p1 [Non-Patent Document 2] Ferreboeuf et al.,HumanMolecular Genetics 2013,Vol.23(1),p171 [Non-Patent Document 3] Sacconi et al., Biochim. Biophys. Acta 2015, p607 Summary of the Invention [Problem to be solved by the invention]

[0012] It is an object of the present invention to provide compounds, methods, and pharmaceutical compositions for inhibiting the expression of DUX4 and for treating, i.e., curing, preventing, delaying, or ameliorating, DUX4-related diseases and / or symptoms thereof. The compounds and pharmaceutical compositions disclosed herein also inhibit mutant forms of DUX4, such as SNPs, and splicing variants of DUX4. [Means for solving the problem]

[0013] Certain embodiments provide a method of reducing expression of DUX4 in an animal (including a human), comprising administering to the animal a compound containing a modified oligonucleotide targeting DUX4, or a pharmaceutical composition containing the compound, as described herein.

[0014] Certain embodiments provide methods for administering to an animal a compound or pharmaceutical composition containing a modified oligonucleotide targeting DUX4 to knockdown the protein via a nuclear ribonuclease (such as RNase H). Also provided are methods for administering a compound containing the modified oligonucleotide to inhibit transcription of DUX4 mRNA or translation of DUX4 protein. The modified oligonucleotide is preferably distributed to muscle, and more preferably distributed to skeletal muscle.

[0015] Certain embodiments provide a method for treating an animal with FSHD. In certain embodiments, the method of the present invention comprises administering to the animal a therapeutically effective amount of a compound or pharmaceutical composition comprising a modified oligonucleotide targeting DUX4, as further described herein. In certain embodiments, the method of the present invention comprises identifying an animal with FSHD1 and / or FSHD2.

[0016] Certain embodiments provide a method for treating, i.e., curing, preventing, delaying, or improving muscle atrophy and muscle weakness. The aim is to alleviate or delay the worsening of symptoms such as poor facial expression, sleeping with eyes open, difficulty in lifting arms, and winged scapula due to muscle weakness in the face, cheeks, shoulders, and upper arms. It is also preferable to prevent muscle weakness in the pelvic girdle and lower limbs, and further prevent complications such as nerve hearing loss and retinopathy.

[0017] In certain embodiments, DUX4 mRNA has a sequence set forth in GenBank Accession No. NM_001293798.2 (herein incorporated as SEQ ID NO: 1 in the sequence listing). The splice variant of DUX4 mRNA of SEQ ID NO: 1 in the sequence listing is also referred to as DUX4-FL1 or mature mRNA of DUX4. In certain embodiments, DUX4 mRNA has a sequence set forth in GenBank Accession No. NM_001306068.2 (herein incorporated as SEQ ID NO: 5 in the sequence listing). The splice variant of DUX4 mRNA of SEQ ID NO: 5 in the sequence listing is also referred to as DUX4-FL2. In certain embodiments, DUX4 has a sequence set forth in GenBank Accession No. NM_001363820.1 (herein incorporated as SEQ ID NO: 6 in the sequence listing). The splice variant of DUX4 mRNA of SEQ ID NO: 6 in the sequence listing is also referred to as DUX4-s. In certain embodiments, DUX4 refers to the SNP of said splice variant.

[0018] The present disclosure relates to, but is not limited to, the non-limiting numbered embodiments described in sections [1] to

[27] below.

[0019] Item [1] A modified oligonucleotide consisting of 12 to 30 residues, a sequence of at least 8 contiguous nucleobases, which is complementary to an isometric portion of the nucleobase sequence of DUX4 mature mRNA of SEQ ID NO: 1 at positions 126-147, 232-248, 1306-1325, or 1480-1495 from the 5' end thereof; the nucleobase sequence of the modified oligonucleotide has at least 90% complementarity to an equal length portion of the nucleobase sequence of the mature mRNA of DUX4 of SEQ ID NO:1; When the sequence of at least 8 consecutive nucleobases includes a nucleobase sequence complementary to an equal length portion of the nucleobase sequence of SEQ ID NO: 1 at positions 1480 to 1495 from the 5' end, the modified oligonucleotide is composed of a nucleobase sequence having a complementary base of the nucleobase sequence of SEQ ID NO: 1 at its 3' end, the complementary base of the base at position 1480 from the 5' end of the nucleobase sequence of SEQ ID NO: 1. Modified oligonucleotides.

[0020] Item [2] The modified oligonucleotide according to item [1], wherein one or more modified nucleotides in the modified oligonucleotide include a modified sugar. Item [3] The modified oligonucleotide according to item [2], wherein the modified sugar is selected from the group consisting of a bicyclic sugar, a 2'-O-methoxyethyl modified sugar, and a 2'-O-methyl modified sugar. Item [4] The modified oligonucleotide according to item [3], wherein the bicyclic sugar is selected from the group consisting of LNA, GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz], and ALNA[Trz].

[0021] Item [5] A modified oligonucleotide consisting of 12 to 30 residues, A sequence of at least 8 contiguous nucleobases, which is complementary to an equal length portion of the nucleobase sequence of DUX4 mature mRNA of SEQ ID NO: 1 at positions 1472 to 1495 from the 5' end thereof, the nucleobase sequence of the modified oligonucleotide has at least 90% complementarity to an equal length portion of the nucleobase sequence of the mature mRNA of DUX4 of SEQ ID NO:1; the modified oligonucleotide comprises at least one nucleoside comprising a modified sugar selected from GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz], and ALNA[Trz]; Modified oligonucleotides.

[0022] Item [6] The modified oligonucleotide according to item [5], wherein the modified oligonucleotide further comprises a 2'-O-methoxyethyl modified sugar and / or a 2'-O-methyl modified sugar.

[0023] Item [7] The modified oligonucleotide according to any one of claims 1 to 6, wherein at least one modified nucleotide in the modified oligonucleotide comprises a modified nucleic acid base. Item [8] The modified oligonucleotide according to item [7], wherein the modified nucleobase is 5-methylcytosine.

[0024] Item [9] The modified oligonucleotide according to any one of items [1] to [8], wherein at least one internucleoside bond is a modified internucleoside bond. Item

[10] The modified oligonucleotide according to item [9], wherein the modified internucleoside bond is a phosphorothioate internucleoside bond.

[0025] Item

[11] The modified oligonucleotide, 1) a gap segment; 2) a 5' wing segment; and 3) a 3' wing segment, the gap segment is positioned between the 5' wing segment and the 3' wing segment; each nucleoside in the 5' wing segment and the 3' wing segment comprises at least one modified sugar; The modified oligonucleotide according to any one of items [1] to

[10] , wherein the nucleosides in the gap segment are only nucleosides that do not contain a modified sugar, or the gap segment contains one or two nucleosides that contain a modified sugar and the rest are nucleosides that do not contain a modified sugar.

[0026] Item

[12] The modified oligonucleotide, The nucleic acid sequence of the mature mRNA of DUX4 of SEQ ID NO:1 A nucleic acid sequence from 128 to 143 positions from the 5' end, A nucleic acid sequence from 232 to 247 positions from the 5' end, A nucleic acid sequence from 233 to 248 positions from the 5' end, A nucleic acid sequence from positions 1309 to 1323 from the 5' end, or A nucleic acid sequence from 1480 to 1495 positions from the 5' end, The modified oligonucleotide according to any one of items [1] to

[11] , which comprises a nucleic acid base sequence complementary to:

[0027] Item

[13] The modified oligonucleotide, gtggcgatgc ccgggt (SEQ ID NO: 75), gagattcccg cnggtg (SEQ ID NO:78: n represents 5-methylcytosine), ngagattcccgccggt (SEQ ID NO:2: n represents 5-methylcytosine), gnagttctccgcggt (SEQ ID NO:3: n represents 5-methylcytosine), or gnntagacagcgtngg (SEQ ID NO: 4: n represents 5-methylcytosine) The modified oligonucleotide according to any one of items [1] to

[12] , which consists of the base sequence:

[0028] Term

[14] Below formula: GlsMlsMlsTdsAdsGdsAdsCdsAdsGdsCdsGdsTdsMlsGlsGl; The modified oligonucleotide according to item

[13] , During the ceremony, Each nucleobase is represented by the following symbol: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: l=LNA, d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: Shown according to s=phosphorothioate.

[0029] Term

[15] Below formula: GmsMmsMmsTdsAdsGdsAdsCdsAdsGdsCdsGdsTdsMmsGmsGm; The modified oligonucleotide according to item

[13] , During the ceremony, Each nucleobase is represented by the following symbol: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: m=ALNA[Ms], d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: Shown according to s=phosphorothioate.

[0030] Term

[16] Below formula: GmsMmsAmsGdsTdsTdsCdsTdsCdsCdsGdsCdsGmsGmsTm; The modified oligonucleotide according to item

[13] , During the ceremony, Each nucleobase is represented by the following symbol: Designated according to: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine; Each sugar moiety has the following symbol: m=ALNA[Ms], d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: s = phosphorothioate As shown in the figure.

[0031] Term

[17] Below formula: MlsGlsAlsGdsAdsTdsTdsCdsCdsCdsGdsCdsCdsGlsGlsTl; The modified oligonucleotide according to item

[13] , During the ceremony, Each nucleobase is represented by the following symbol: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: l=LNA, d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: s = phosphorothioate As shown in the figure.

[0032] Term

[18] Below formula: [ka] The modified oligonucleotide or a salt thereof according to item

[14] , wherein the modified oligonucleotide is represented by the formula:

[0033] Term

[19] Below formula: [ka] The modified oligonucleotide or a salt thereof according to item

[15] ,

[0034] Term

[20] Below formula: [ka] The modified oligonucleotide or a salt thereof according to item

[16] ,

[0035] Term

[21] Below formula: [ka] The modified oligonucleotide or a salt thereof according to item

[17] ,

[0036] Item

[22] A pharmaceutical composition comprising the modified oligonucleotide or a pharma- ceutically acceptable salt thereof according to any one of items [1] to

[21] and a pharma- ceutically acceptable carrier.

[0037] Item

[23] The pharmaceutical composition according to item

[22] for treating, preventing, or slowing the progression of a DUX4-related disease.

[0038] Item

[24] The pharmaceutical composition according to item

[23] , wherein the DUX4-related disease is facioscapulohumeral muscular dystrophy.

[0039]

[25] A method for treating, preventing, or delaying the progression of a DUX4-related disease in a subject, comprising administering to a subject in need thereof an effective amount of a modified oligonucleotide according to any one of [1] to

[21] .

[0040] Item

[26] Use of the modified oligonucleotide according to any one of items [1] to

[21] in the manufacture of a medicament for treating, preventing or delaying the progression of a DUX4-related disease.

[0041] Item

[27] Use of the modified oligonucleotide according to any one of items [1] to

[21] for treating, preventing or slowing the progression of a DUX4-related disease. Effect of the Invention

[0042] INDUSTRIAL APPLICABILITY The present invention can provide modified oligonucleotides that are effective in treating diseases such as facioscapulohumeral muscular dystrophy caused by the abnormal expression of the DUX4 gene. [Brief description of the drawings]

[0043] [Figure 1] 1 is a diagram showing the inhibitory effect of DUX4 gene expression by administration of various DUX4 modified oligonucleotides. [Diagram 2] 1 is a diagram showing the inhibitory effect of DUX4 gene expression by administration of various DUX4 modified oligonucleotides. [Diagram 3] 1 is a graph showing the dose-dependent inhibitory effect of DUX4 gene expression by administration of DUX4-modified oligonucleotides. [Figure 4] 1 is a diagram showing the inhibitory effect of DUX4 gene expression by administration of various DUX4 modified oligonucleotides. [Diagram 5] FIG. 1 shows the inhibitory effect of creatine kinase and DUX4 mRNA in DUX4 Tg mice by administration of a DUX4-modified oligonucleotide (Compound No. 3). [Figure 6] 1 is a diagram showing the inhibitory effect of creatine kinase and DUX4 mRNA in DUX4 Tg mice by administration of DUX4 modified oligonucleotides (Compound No. 123, Compound No. 247, and Compound No. 113). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0044] It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention as claimed. Herein, the use of the singular includes the plural unless specifically stated otherwise. Herein, the use of "or" means "and / or" unless specifically stated otherwise. Furthermore, the use of the term "including" as well as other forms such as "includes" and "included" is not limiting. Furthermore, unless specifically stated otherwise, terms such as "element" encompass elements that include one unit and elements that include more than one subunit.

[0045] The section headings used herein are for organizational purposes only and should not be construed as limiting the subject matter described. All documents or portions of documents cited in this application, including but not limited to patents, patent applications, articles, books, and papers, are expressly incorporated herein by reference in their entirety and with respect to the portions of the documents discussed herein.

[0046] (definition) Unless specific definitions are given, the nomenclature used in connection with analytical chemistry, organic synthetic chemistry, and medicinal and pharmaceutical chemistry described herein, and the procedures and techniques thereof, are well known and commonly used in the art. Standard techniques can be used for chemical synthesis and chemical analysis used herein. Where permitted, all patents, applications, published applications and other publications, GenBank accession numbers and related sequence information available through databases such as the National Center for Biotechnology Information (NCBI), and other data referred to throughout this disclosure are incorporated by reference in their entirety and with respect to portions of the documents discussed herein. This specification is also filed with a Sequence Listing in electronic format, the information in the Sequence Listing set forth in said electronic format being incorporated herein by reference in its entirety.

[0047] Unless otherwise stated, the following terms have the following meanings.

[0048] "Nucleic acid" refers to a molecule composed of monomeric nucleotides. Examples of nucleic acids include, but are not limited to, ribonucleic acid (RNA), deoxyribonucleic acid (DNA), single-stranded nucleic acid, double-stranded nucleic acid, small interfering ribonucleic acid (siRNA), and microRNA (miRNA). Nucleic acids can also include combinations of these elements in a single molecule.

[0049] "Nucleobase" means a heterocyclic moiety capable of pairing with a base of another nucleic acid. Nucleobases include "modified nucleobases" and "unmodified nucleobases."

[0050] "Nucleobase sequence" means the contiguous order of nucleobases independent of any sugar linkages or nucleobase modifications.

[0051] "Nucleoside" means a nucleobase linked to a sugar. In certain embodiments, the nucleoside is linked to a phosphate group.

[0052] "Nucleotide" refers to a nucleoside having, for example, a phosphate group covalently bonded to the sugar portion of the nucleoside. Naturally occurring nucleotides have a sugar portion of ribose or deoxyribose, which is covalently bonded via the phosphate group by a phosphodiester bond.

[0053] "Oligomeric compound" or "oligomer" means a polymer of linked monomeric subunits that is capable of hybridizing to at least a region of a nucleic acid molecule.

[0054] "Oligonucleotide" means a polymer of linked nucleosides, in which each nucleoside and each internucleoside linkage, independently of the others, can be modified or unmodified.

[0055] "Unmodified nucleotide" refers to a nucleotide consisting of naturally occurring nucleobases, sugar moieties, and internucleoside linkages. In certain embodiments, an unmodified nucleotide is an RNA nucleotide (i.e., β-D-ribonucleoside) or a DNA nucleotide (i.e., β-D-deoxyribonucleoside), but is not limited to such.

[0056] "Modified nucleotide" means a nucleotide having, independently, a modified sugar moiety, modified internucleoside linkage, or modified nucleobase. "Modified nucleoside" means a nucleoside having, independently, a modified sugar moiety or modified nucleobase.

[0057] "Internucleoside linkage" refers to the chemical bond between nucleosides.

[0058] "Linked nucleosides" means adjacent nucleosides that are joined or linked by an internucleoside bond.

[0059] "Naturally occurring internucleoside linkage" means a 3'-5' phosphodiester linkage.

[0060] "Modified internucleoside linkage" refers to a substitution or any change from a naturally occurring internucleoside linkage (i.e., a phosphodiester internucleoside linkage), such as, but not limited to, a phosphorothioate internucleoside linkage.

[0061] "Phosphorothioate internucleoside linkage" means a linkage between nucleosides in which the phosphodiester bond is modified by replacing one of the non-bridging oxygen atoms with a sulfur atom. A phosphorothioate linkage is one example of such a modified internucleoside linkage.

[0062] "Modified nucleobase" refers to any nucleobase other than adenine, cytosine, guanine, thymidine, or uracil, including, but not limited to, 5-methylcytosine. "Unmodified nucleobase" refers to the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C), and uracil (U).

[0063] "Modified oligonucleotide" means an oligonucleotide containing at least one modified nucleoside and / or modified internucleoside linkage. "Salt" is a general term for a compound in which one or more dissociable hydrogen ions contained in an acid are replaced with a cation such as a metal ion or ammonium ion. Examples of salts of modified oligonucleotides include, but are not limited to, salts (e.g., sodium salts, magnesium salts) formed with inorganic ions (e.g., sodium ions, magnesium ions) on the thio (S) group of a phosphorothioate bond or on a functional group (e.g., an amino group) in a modified nucleic acid base.

[0064] "Sugar" or "sugar moiety" means a naturally occurring sugar moiety or a modified sugar moiety.

[0065] "Natural sugar moiety" means a sugar found in DNA (2'-H) or RNA (2'-OH).

[0066] "Modified sugars" refer to substitutions or changes from a natural sugar moiety. Modified sugars include, for example, substituted sugar moieties and sugar substitute moieties.

[0067] "Substituted sugar moiety" means a furanosyl other than the natural sugars of RNA or DNA.

[0068] "2'-O-Methoxyethyl" (also 2'-MOE and 2'-O(CH2)2-OCH3) refers to an O-methoxy-ethyl modification at the 2' position of the furanosyl ring. A 2'-O-methoxyethyl modified sugar is a modified sugar.

[0069] "2'-O-methoxyethyl nucleotide" means a nucleotide containing a 2'-O-methoxyethyl modified sugar moiety.

[0070] "2'-O-methyl" (also 2'-OMe and 2'-OCH3) refers to an O-methyl modification at the 2' position of the furanosyl ring. A 2'-O-methyl modified sugar is a modified sugar.

[0071] "2'-O-methyl nucleotide" means a nucleotide containing a sugar moiety that is 2'-O-methyl modified.

[0072] "Sugar surrogate" for "sugar substitute moiety" is intended to refer to the replacement of the sugar unit (furanose ring) only. Sugar surrogates can replace the naturally occurring sugar moiety of a nucleoside, such that the resulting nucleoside subunits can be linked to each other and / or to other nucleosides to form oligomeric compounds that can hybridize to complementary oligomeric compounds. Such structures include rings containing different numbers of atoms than furanosyl (e.g., 4-, 6-, or 7-membered rings); replacement of oxygen of furanosyl with non-oxygen atoms (e.g., carbon, sulfur, or nitrogen); or both change in the number of atoms and replacement of oxygen. Such structures can also include substitutions corresponding to those described for the substituted sugar moiety (e.g., 6-membered carbocyclic bicyclic sugar surrogates optionally containing additional substituents). Sugar surrogates also include more complex sugar replacements (e.g., non-cyclic peptide nucleic acids). Sugar surrogates include, but are not limited to, morpholino, cyclohexenyl, and cyclohexitol.

[0073] "Bicyclic sugar" refers to a furanosyl ring modified by bridging two different carbon atoms present on the same ring. Preferably, "bicyclic sugar" refers to a modified sugar in which the 2' and 4' positions of the furanosyl ring are modified by bridging. "Bicyclic nucleic acid" refers to a nucleoside or nucleotide in which the furanose portion of the nucleoside or nucleotide contains a "bicyclic sugar."

[0074] "LNA" refers to a nucleoside or nucleotide commonly referred to as 2',4'-locked nucleic acid, for example, a nucleoside having the general formula: [ka] [In the formula, B is a nucleobase; X and Y are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, etc. (See WO98 / 39352.) A typical example is a nucleoside or nucleotide represented by the following formula: [ka] Examples of such nucleotides include those represented by the formula:

[0075] "GuNA" has the following formula: [ka] [In the formula, B is a nucleic acid base, and R3, R4, R5, and R6 are each independently a hydrogen atom or a C 1-6 R7 and R8 are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a covalent bond to a phosphorus moiety or a support, and R9 and R 10 , R 11 Each independently represents a hydrogen atom or C which may be substituted with one or more substituents. 1-6 It is a protecting group for an alkyl group or an amino group. (See, for example, International Publication No. WO 2014 / 046212 and International Publication No. WO 2017 / 047816).

[0076] "ALNA[mU]" is represented by the following general formula (I): [ka] [In the formula, B is a nucleobase; R1, R2, R3 and R4 each independently represent a hydrogen atom or a C 1-6 is an alkyl group; R5 and R6 are each independently a hydrogen atom, a protecting group for a hydroxyl group, or an optionally substituted phosphate group, a covalent bond to a phosphorus moiety or support, or the like; m is 1 or 2; X is represented by the following formula (II-1): [ka] is a group represented by the formula: The symbols shown in formula (II-1): [ka] indicates the point of attachment to the 2'-amino group; One of R7 and R8 is a hydrogen atom, and the other is a methyl group which may be substituted with one or more substituents. (See, for example, Japanese Patent Application No. 2018-212424.) A typical example is a nucleoside or nucleotide in which one of R7 and R8 is a hydrogen atom and the other is an unsubstituted methyl group.

[0077] "ALNA[ipU]" is a nucleoside or nucleotide represented by the general formula (I) as defined above in "ALNA[mU]", wherein: X is represented by the following formula (II-1): [ka] is a group represented by the formula: One of R7 and R8 is a hydrogen atom, and the other is an isopropyl group which may be substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example is a nucleoside or nucleotide in which one of R7 and R8 is a hydrogen atom, and the other is an unsubstituted isopropyl group.

[0078] "ALNA[Trz]" is a nucleoside or nucleotide represented by the general formula (I) defined above in "ALNA[mU]", wherein: X is represented by the following formula (II-2): [ka] is a group represented by the formula: A is a triazolyl group optionally substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example is a nucleoside or nucleotide in which A is a triazolyl group optionally having one or more methyl groups, more specifically a 1,5-dimethyl-1,2,4-triazol-3-yl group.

[0079] "ALNA[Oxz]" is a nucleoside or nucleotide represented by the general formula (I) defined above in "ALNA[mU]", wherein: X is represented by the following formula (II-2): [ka] is a group represented by the formula: A is an oxadiazolyl group optionally substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example is a nucleoside or nucleotide in which A is an oxadiazolyl group optionally having one or more methyl groups, more specifically, a 5-methyl-1,2,4-oxadiazol-3-yl group.

[0080] "ALNA[Ms]" is a nucleoside or nucleotide represented by the general formula (I) defined above in "ALNA[mU]", wherein: X is represented by the following formula (II-3): [ka] is a group represented by the formula: M is a sulfonyl group substituted with a methyl group which may be substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example is a nucleoside or nucleotide in which M is a sulfonyl group substituted with an unsubstituted methyl group.

[0081] "5-methylcytosine" means a cytosine modified with a methyl group attached to position 5. 5-methylcytosine is a modified nucleobase.

[0082] "Single-stranded oligonucleotide" means an oligonucleotide that is not hybridized to a complementary strand.

[0083] "DUX4" refers to a nucleic acid or protein of a transcription factor also known as double homeobox 4. DUX4 includes, for example, various splicing variants transcribed from the DUX4 gene, or single nucleotide polymorphisms (SNPs) thereof, and may be the variants and / or SNPs.

[0084] Many splicing variants have been reported for DUX4 mRNA. Human DUX4-s (SEQ ID NO: 6 in the sequence listing) consists of a short exon 1 (exon 1s), exon 2, and exon 3 due to an atypical splicing donor site in exon 1, and encodes a short, non-toxic DUX4 protein. Human DUX4-FL consists of exons 1, 2, and 3, and encodes the full-length DUX4 protein. DUX4-FL includes DUX4-FL1 (SEQ ID NO: 1 in the sequence listing), which is a mature mRNA that does not contain intron 1, and DUX4-FL2 (SEQ ID NO: 5 in the sequence listing), which contains intron 1. Both of these encode the full-length DUX4 protein, and when expressed in muscle, they are considered to be the cause of FSHD (see Non-Patent Document 2).

[0085] DUX4 mRNA is also expressed in normal testes, but in addition to DUX4-FL, splicing variants of exon 1, exon 2, exon 6, and exon 7, and / or splicing variants of exon 1, exon 2, exon 4, exon 5, exon 6, and exon 7 are expressed (see Non-Patent Document 1, supra).

[0086] DUX4 protein functions as a transcription factor, and examples of genes whose transcription is regulated by DUX4 include MBD3L2, ZSCAN4, TRIM43, DEFB103, and ZNF217 (see Non-Patent Document 2 mentioned above).

[0087] The DUX4 mRNA targeted by the modified oligonucleotide of the present invention is preferably human DUX4, more preferably DUX4-FL, and even more preferably DUX4-FL1 set forth in SEQ ID NO: 1 in the sequence listing. In addition, the target sites of the modified oligonucleotide of the present invention for DUX4 are preferably exon 1, intron 1, exon 2, intron 2, or exon 3.

[0088] It is known that the DUX4 gene is expressed by fusing with other genes due to chromosomal abnormalities such as translocation. Other genes, such as IGH (Yasuda et al., Nature Genetics 48(5), 569(2016)), CIC (Yoshimoto et al., Cancer research 77, 2927(2017)), and EWSR1 (Sirvent et al., Cancer Genetics and Cytogenetics 195, 12(2009)), have been reported, and are considered to be causative genes for B-cell acute lymphoblastic leukemia, differentiated round cell sarcoma, and embryonal rhabdomyosarcoma, respectively. The modified oligonucleotide of the present invention also includes compounds that target these fusion genes.

[0089] "Expression of DUX4" refers to the level of mRNA transcribed from the gene encoding DUX4 or the level of protein translated from that mRNA. Expression of DUX4 can be determined by methods known in the art, such as Northern or Western blot, PCR, etc.

[0090] "DUX4 nucleic acid" refers to any nucleic acid encoding DUX4. For example, in certain embodiments, DUX4 nucleic acid includes DNA sequences encoding DUX4, RNA sequences transcribed from DNA encoding DUX4 (including genomic DNA including introns and exons), and pre-mRNA or spliced ​​mature mRNA encoding DUX4. In certain embodiments, DUX4 nucleic acid also includes DNA and RNA sequences of genes resulting from fusion of the DUX4 gene with other genes.

[0091] "DUX4 mRNA" means an mRNA encoding the DUX4 protein.

[0092] "Contiguous nucleobases" and "contiguous nucleobases" mean nucleobases immediately adjacent to one another.

[0093] "Complementary" means the capacity for pairing between nucleobases of a first nucleic acid and a second nucleic acid.

[0094] "Fully complementary" or "100% complementary" means that every nucleobase of a nucleobase sequence of a first nucleic acid has a complementary nucleobase in a second nucleobase sequence of a second nucleic acid. In certain embodiments, the first nucleic acid is a modified oligonucleotide and the target nucleic acid is the second nucleic acid.

[0095] "Hybridization" refers to the annealing of complementary nucleic acid molecules. In certain embodiments, complementary nucleic acid molecules include modified oligonucleotides and target nucleic acids.

[0096] "Specifically hybridizable" refers to a modified oligonucleotide that has a sufficient degree of complementarity between the modified oligonucleotide and the target nucleic acid to induce a desired effect, while exhibiting minimal or no effect on non-target nucleic acids under conditions where specific binding is desired, i.e., physiological conditions in the case of in vivo assays and therapeutic treatments.

[0097] A "mismatch" or "non-complementary nucleobase" refers to the case where a nucleobase of a first nucleic acid fails to pair with the corresponding nucleobase of a second or target nucleic acid.

[0098] "Targeting" or "targeted" refers to the process of design and selection of modified oligonucleotides that will specifically hybridize to a target nucleic acid and induce a desired effect.

[0099] "Target nucleic acid," "target RNA," and "target RNA transcript" all refer to a nucleic acid to which a modified oligonucleotide can be targeted. In certain embodiments, the target nucleic acid comprises a region of a DUX4 nucleic acid.

[0100] "Target segment" refers to the nucleotide sequence of a target nucleic acid to which a modified oligonucleotide is targeted. "5' target site" refers to the 5'-most nucleotide of a target segment. "3' target site" refers to the 3'-most nucleotide of a target segment.

[0101] "Active target region" or "target region" refers to a region targeted by one or more active modified oligonucleotides. "Active modified oligonucleotide" refers to a modified oligonucleotide that reduces target nucleic acid levels or protein levels.

[0102] "Antisense inhibition" means a reduction in the level of a target nucleic acid or a target protein in the presence of a modified oligonucleotide complementary to a target nucleic acid compared to the level of the target nucleic acid or the target protein in the absence of the modified oligonucleotide.

[0103] "siRNA" means a double-stranded RNA oligonucleotide having a nucleobase sequence that allows hybridization to a corresponding region or segment of a target nucleic acid.

[0104] "shRNA" means a hairpin-shaped single-stranded RNA oligonucleotide having a nucleobase sequence that allows hybridization to a corresponding region or segment of a target nucleic acid.

[0105] "snoRNA" refers to a non-coding RNA present in the nucleolus, a single-stranded oligonucleotide that has a nucleic acid base sequence that allows hybridization to a corresponding region or segment of a target RNA nucleic acid and directs chemical modification of the target RNA nucleic acid by methylation or pseudouridylation.

[0106] "miRNA" is a non-coding RNA that regulates the expression of other genes and refers to a single- or double-stranded RNA oligonucleotide having a nucleobase sequence that allows hybridization to a corresponding region or segment of a target nucleic acid.

[0107] "Cap structure" or "terminal capping moiety" means a chemical modification incorporated at either end of a modified oligonucleotide.

[0108] A "chemically heterogeneous region" refers to a region in a modified oligonucleotide that is chemically different in some way from another region in the same modified oligonucleotide. For example, a region having 2'-O-methoxyethyl nucleotides is chemically different from a region having nucleotides that are not 2'-O-methoxyethyl modified.

[0109] "Chimeric modified oligonucleotide" means a modified oligonucleotide that has at least two chemically heterogeneous regions.

[0110] "Motif" means a pattern of chemically heterogeneous regions in modified oligonucleotides.

[0111] "Gapmer" means a modified oligonucleotide in which an internal region having multiple nucleosides that supports cleavage by RNase H is located between external regions having one or more nucleosides, and the nucleosides that make up the internal region are chemically distinct from the nucleoside(s) that make up the external regions. The internal region can be referred to as the "gap segment" and the external regions can be referred to as the "wing segment." A wing segment that is 5' from the gap segment can be referred to as the "5' wing segment" and a wing segment that is 3' from the gap segment can be referred to as the "3' wing segment."

[0112] "Directly adjacent" means that there are no intervening elements between the immediately adjacent elements.

[0113] "Nuclear ribonuclease" means a ribonuclease found in the nucleus, including, but not limited to, RNase H, including RNase H1 and RNase H2, double-stranded RNase Drosha, and other double-stranded RNases.

[0114] In certain embodiments, a gapmer refers to a modified oligonucleotide having 5' and 3' wing segments, each of one to eight nucleosides, and a gap segment of six or more nucleosides located between and directly adjacent to the wing segments, which gap segment either contains only nucleosides without modified sugars or contains one or two nucleosides that contain modified sugars and the rest do not contain modified sugars.

[0115] "Drug" refers to an active substance capable of providing a therapeutic benefit when administered to an animal. "First drug" refers to a therapeutic compound of the invention. For example, a first drug can be a modified oligonucleotide that targets DUX4. "Second drug" refers to a second therapeutic compound of the invention (e.g., a second modified oligonucleotide that targets DUX4) and / or a therapeutic compound that does not target DUX4.

[0116] "Pharmaceutically acceptable salts" means physiologically and pharma- ceutical acceptable salts of modified oligonucleotides, i.e., salts that retain the desired biological activity of the modified oligonucleotide and do not impart undesired toxicological effects thereto.

[0117] "Diluent" means an ingredient in a composition that lacks pharmacological activity, but is medicamentously necessary or desirable. For example, a diluent in a composition to be injected may be a liquid, such as saline.

[0118] "DUX4-related disease" refers to a disease caused by abnormal expression of DUX4 mRNA or DUX4 protein, or the mRNA or protein of a fusion gene due to translocation of the DUX4 gene. Facioscapulohumeral muscular dystrophy, B-cell acute lymphoblastic leukemia, differentiated round cell sarcoma, embryonal rhabdomyosarcoma, etc. are included, but are not limited to these.

[0119] "Facioscapulohumeral muscular dystrophy" or "FSHD" refers to a muscular dystrophy that develops from muscle weakness in the facial, scapular and upper arm muscles. In humans, it is thought that this condition is mainly caused by shortening of the genomic repeat sequence (D4Z4) near the telomere (end of the chromosome) of chromosome 4, which results in a change in the genome structure, and the DUX4 gene, which is not normally expressed in muscle (progenitor) cells, is ectopically expressed, causing cell death (FSHD1). In addition, gene mutations have been found in some FSHD patients in SMCHD1, one of the genome structure control factors that suppress gene expression (FSHD2).

[0120] FSHD is a type of muscular dystrophy associated with progressive muscle weakness and muscle fiber loss. Unlike Duchenne and Becker muscular dystrophy, which primarily affect the lower body, FSHD affects the upper body, primarily the facial, scapular, and upper arm muscles. However, it can also affect the pelvis, lower back, and lower legs. Symptoms of FSHD often appear between the ages of 10 and 26, but can occur much later. In some cases, they may never appear at all. Symptoms are usually mild and worsen very slowly. Facial muscle weakness is common, and symptoms may include ptosis, inability to whistle, reduced facial expression, depressed or angry facial expressions, difficulty pronouncing words, scapular muscle weakness (leading to deformities such as winged scapula and round shoulders), lower limb weakness, hearing loss, and possible heart disease.

[0121] "Active pharmaceutical agent" refers to the substance or substances in a pharmaceutical composition that provide a therapeutic benefit when administered to an animal. For example, in certain embodiments, a modified oligonucleotide targeting DUX4 is an active pharmaceutical agent.

[0122] "Administered simultaneously" refers to the co-administration of two drugs in any manner in which the pharmacological effects attributable to both drugs are expressed in a patient at the same time. Simultaneous administration does not require that both drugs are administered in a single pharmaceutical composition, in the same dosage form, or by the same route of administration. The pharmacological effects attributable to both drugs do not have to be expressed at the same time. The pharmacological effects only need to overlap within a certain period of time, and do not have to be coextensive.

[0123] "Administering" means giving an agent to an animal and includes, but is not limited to, administration by a medical professional and self-administration.

[0124] "Amelioration" refers to a reduction in at least one indicator, sign or symptom of the associated disease, disorder or condition. The severity of the indicator can be determined by subjective or objective measures known to those skilled in the art.

[0125] "Animal" refers to a human or non-human animal, including, but not limited to, mice, rats, rabbits, dogs, cats, pigs, and non-human primates, including, but not limited to, monkeys and chimpanzees.

[0126] "Co-administration" refers to the administration of two or more agents to an individual. The two or more agents may be present in a single pharmaceutical composition or in separate pharmaceutical compositions. Each of the two or more agents may be administered via the same or different routes of administration. Co-administration encompasses concurrent or sequential administration.

[0127] "Dose" refers to a specific amount of a pharmaceutical agent given in a single administration or over a specific period of time. In certain embodiments, a dose can be administered in one, two or more boluses, tablets, or injections. For example, in certain embodiments where subcutaneous administration is desired, the desired dose requires a volume that is not easily accommodated in a single injection, so two or more injections can be used to achieve the desired dose. In certain embodiments, a pharmaceutical agent is administered over an extended period of time or continuously by infusion. A dose can be described as the amount of pharmaceutical agent per hour, day, week, or month.

[0128] "Effective amount" or "therapeutically effective amount" refers to an amount of an active pharmaceutical agent that is sufficient to achieve a desired physiological outcome in an individual in need of the agent. The effective amount may vary from individual to individual, depending on the health and physical condition of the individual being treated, the taxonomic group of the individual being treated, the formulation of the composition, an evaluation of the individual's medical condition, and other relevant factors.

[0129] "Identifying an animal with facioscapulohumeral muscular dystrophy (FSHD)" means identifying an animal that has been diagnosed with an FSHD disorder or condition, or identifying an animal that is predisposed to an FSHD disorder or condition. For example, an individual with a family history may be predisposed to an FSHD disorder or condition. Such identification can be achieved by any method, including examining the individual's medical history and standard clinical tests or evaluations. FSHD includes both FSHD1 and FSHD2, which are known depending on the pathogenic mechanism.

[0130] "Individual" means a human or non-human animal selected for treatment or therapy.

[0131] "Myotonia" refers to abnormally slow muscle relaxation after voluntary contraction or electrical stimulation.

[0132] "Parenteral administration" means administration via injection or infusion. Parenteral administration includes subcutaneous, intravenous, intramuscular, intraarterial, intraperitoneal or intracranial administration, e.g., intrathecal or intraventricular. Administration may be continuous or chronic, brief or intermittent.

[0133] "Pharmaceutical composition" means a mixture of substances suitable for administration to an individual. For example, a pharmaceutical composition can include one or more active agents and a sterile aqueous solution.

[0134] "Prevent" means to delay or forestall the onset or occurrence of a disease, disorder, or adverse health condition, or one or more symptoms associated with the disease, disorder, or adverse health condition, for a period ranging from minutes to an indefinite period. Prevent can also mean to reduce the risk of developing a disease, disorder, or adverse health condition.

[0135] "Treating" means alleviating or eliminating a disease, disorder or adverse health condition, or one or more symptoms associated with the disease, disorder or adverse health condition, or partially resolving or eradicating one or more causes of the disease, disorder or adverse health condition itself.

[0136] "Treating" is intended to include prevention or therapy as described above, including, for example, administering a pharmaceutical composition of the present invention to effect an alteration or improvement of the disease, disorder, or adverse health condition.

[0137] "Prodrug" means a therapeutic agent that is prepared in an inactive form that is converted to an active form within the body or cells thereof by the action of endogenous enzymes or other chemicals or conditions.

[0138] "Side effects" refers to physiological responses that may result from treatment other than the desired effect. In certain embodiments, side effects include injection site reactions, abnormal liver function tests, renal dysfunction, hepatotoxicity, nephrotoxicity, central nervous system abnormalities, myopathy, and fatigue. For example, elevated levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), or gamma-glutamyl transpeptidase (gamma-GTP) in the blood may indicate hepatotoxicity or hepatic dysfunction. For example, elevated bilirubin may indicate hepatotoxicity or hepatic dysfunction. Also, elevated urinary protein, elevated blood creatinine, and elevated urea nitrogen (UN) may indicate nephrotoxicity or renal dysfunction.

[0139] "Subcutaneous administration" means administration just beneath the skin.

[0140] "Therapeutically effective amount" means an amount of a drug that confers a therapeutic benefit on an individual.

[0141] (Specific embodiment) Implementation Certain specific embodiments, including but not limited to those set forth below, provide compounds, methods of using the compounds, and pharmaceutical compositions containing the compounds for inhibiting expression of DUX4.

[0142] Certain embodiments provide methods of reducing expression of DUX4 in an animal comprising administering to the animal a compound containing a modified oligonucleotide that targets DUX4.

[0143] Certain embodiments provide methods of administering modified oligonucleotides to prevent the accumulation of pathogenic DUX4 transcription factor by inhibiting transcription of the DUX4 gene, or inhibiting translation of DUX4 mRNA, or inducing cleavage of DUX4 mRNA.

[0144] Certain embodiments provide a method of treating an animal having facioscapulohumeral muscular dystrophy, comprising the steps of: a) identifying the animal having facioscapulohumeral muscular dystrophy, and b) administering to the animal a therapeutically effective amount of a compound containing a modified oligonucleotide targeting DUX4.

[0145] Certain embodiments provide a method for reducing myotonia in a subject in need thereof. The method includes administering to the subject a modified oligonucleotide complementary to DUX4 mRNA, which, when bound to DUX4 mRNA, activates ribonuclease or nuclear ribonuclease, thereby reducing myotonia. In certain embodiments, the subject has or is suspected of having facioscapulohumeral muscular dystrophy, or has or is suspected of having high expression of DUX4 mRNA, has a reduced number of D4Z4 repeats on human chromosome 4, or has or is suspected of having SMCHD1 (DNA methyltransferase) mutation.

[0146] In certain embodiments, the modified oligonucleotides used in the methods of the invention are chimeras.In certain embodiments, the modified oligonucleotides used in the methods of the invention are gapmers.

[0147] In certain embodiments of the methods of the invention described herein, the administration is subcutaneous. In certain embodiments, the administration is intravenous or intramuscular.

[0148] In certain embodiments, modified oligonucleotides used in the methods of the invention target the DUX4 protein coding region, an intron, the 5'UTR or the 3'UTR of DUX4 mRNA. In certain embodiments, modified oligonucleotides used in the methods of the invention target exon 1, exon 2, exon 3, intron 1 or intron 2 of DUX4 mRNA.

[0149] In certain embodiments of the methods of the invention described herein, DUX4 mRNA is cleaved by the nuclear ribonuclease RNase H1.

[0150] In certain embodiments of the method of the present invention, DUX4 mRNA is reduced in muscle tissue. In certain embodiments, splicing variants DUX4-FL1 (SEQ ID NO: 1 in the sequence listing) and DUX4-FL2 (SEQ ID NO: 5 in the sequence listing) are preferentially reduced.

[0151] In certain embodiments, DUX4 mRNA has a sequence set forth in GenBank Accession No. NM_001293798.2 (herein incorporated as SEQ ID NO: 1 in the sequence listing). The splice variant of SEQ ID NO: 1 in the sequence listing is also referred to as DUX4-FL1 or mature mRNA of DUX4. In certain embodiments, DUX4 mRNA has a sequence set forth in GenBank Accession No. NM_001306068.2 (herein incorporated as SEQ ID NO: 5 in the sequence listing). The splice variant of SEQ ID NO: 5 in the sequence listing is also referred to as DUX4-FL2. In certain embodiments, DUX4 has a sequence set forth in GenBank Accession No. NM_001363820.1 (herein incorporated as SEQ ID NO: 6 in the sequence listing). The splice variant of SEQ ID NO: 6 in the sequence listing is also referred to as DUX4-s. In certain embodiments, DUX4 mRNA has the SNPs of the splice variants described above.

[0152] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, and has a nucleobase sequence comprising a modified oligonucleotide that is a nucleobase sequence comprising at least 8 consecutive nucleobases that are complementary to an isometric portion of the nucleobases at positions 126 to 147, 232 to 248, 1306 to 1325, or 1472 to 1495 from the 5' end of the nucleobases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing. In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, and has a nucleobase sequence comprising a modified oligonucleotide that is a nucleobase sequence comprising at least 9, 10, 11, or 12 consecutive nucleobases that are complementary to an isometric portion of the nucleobases at positions 126 to 147, 232 to 248, 1306 to 1325, or 1472 to 1495 from the 5' end of the nucleobases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing. The modified oligonucleotide may consist of a sequence of at least eight consecutive nucleic acid bases that is complementary to an equal-length portion of the nucleic acid bases at positions 126 to 147, 232 to 248, 1306 to 1325, or 1472 to 1495 from the 5' end of the nucleic acid bases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, or may have an additional sequence on the 5' end and / or 3' end in addition to the nucleic acid base sequence.

[0153] In certain embodiments, the modified oligonucleotide is a nucleic acid base sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, or 22 consecutive nucleic acid base sequences that are complementary to an equal-length portion of the nucleic acid bases from positions 126 to 147 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0154] In certain embodiments, the modified oligonucleotide is a nucleobase sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, 16 or 17 consecutive nucleobases that are complementary to an equal length portion of the nucleobases at positions 232 to 248 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0155] In certain embodiments, the modified oligonucleotide is a nucleic acid base sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 consecutive nucleic acid base sequences that are complementary to an equal-length portion of the nucleic acid bases from positions 1306 to 1325 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0156] In certain embodiments, the modified oligonucleotide is a nucleobase sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24 consecutive nucleobases that are complementary to an equal length portion of the nucleobases from positions 1472 to 1495 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0157] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases from positions 126 to 147 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0158] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases at positions 232 to 248 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0159] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases from positions 1306 to 1325 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0160] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases from positions 1472 to 1495 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues , 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0161] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, and has a nucleobase sequence comprising a modified oligonucleotide which is a nucleobase sequence comprising at least 8 consecutive nucleobases complementary to an isometric portion of the nucleobases at positions 128 to 143, 233 to 248, 1309 to 1323, or 1480 to 1495 from the 5' end of the nucleobases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing. In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, and has a nucleobase sequence comprising a modified oligonucleotide which is a nucleobase sequence comprising at least 9, 10, 11, or 12 consecutive nucleobases complementary to an isometric portion of the nucleobases at positions 128 to 143, 233 to 248, 1309 to 1323, or 1480 to 1495 from the 5' end of the nucleobases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing.

[0162] In certain embodiments, the modified oligonucleotide is a nucleobase sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, or 16 consecutive nucleobases that are complementary to an equal length portion of the nucleobases 128 to 143 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0163] In certain embodiments, the modified oligonucleotide is a nucleobase sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, or 16 consecutive nucleobases that are complementary to an equal-length portion of the nucleobases at positions 233 to 248 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0164] In certain embodiments, the modified oligonucleotide is a nucleobase sequence that includes at least 8, 9, 10, 11, 12, 13, 14, or 15 consecutive nucleobases that are complementary to an equal-length portion of the nucleobases at positions 1309 to 1323 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0165] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide of 30 residues or less, consisting of a nucleic acid base sequence of at least 8, 9, 10, 11, 12, 13, 14, 15 or 16 consecutive nucleic acid bases that are complementary to an equal length portion of the nucleic acid bases at positions 1480 to 1495 from the 5' end of the nucleic acid bases of SEQ ID NO: 1 in the sequence listing, and having a complementary base of the base at position 1480 from the 5' end of the nucleic acid bases of SEQ ID NO: 1 at its 3' end.

[0166] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases from positions 128 to 143 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0167] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases at positions 233 to 248 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0168] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases at positions 1309 to 1323 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0169] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues, and has a nucleobase sequence that is complementary to an isometric portion from positions 1480 to 1495 from the 5' end of the nucleobase of DUX4 mature mRNA of SEQ ID NO: 1 in the Sequence Listing, and has a nucleobase sequence having a complementary base of the 1480th base from the 5' end of the nucleobase of SEQ ID NO: 1 at its 3' end, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isometric portion. In addition, in certain embodiments, 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues , 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0170] In certain embodiments, the modified oligonucleotides provided herein target any one of the following regions of SEQ ID NO:1 in the Sequence Listing: 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-143, 128-144, 128-147, 232-245, 232-246, 232-247, 232-248, 232-249, 232-250, 232-251, 232-252, 232-253, 232-254, 232-255, 232-256, 232-257, 232-258, 232-259, 232-259 32~247, 233~246, 233~247, 233~248, 234~247, 234~248, 1304~1323, 1306~1321, 1306~1324, 1307~1323, 1307~1324, 1307~1325, 1307~1326, 1308~1323, 1308~1324, 1308~1322, 130 8~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~1488, 147 4-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein target any one of the following regions of SEQ ID NO: 1 of the Sequence Listing: positions 128-143, 232-247, 233-248, 1309-1323 and 1480-1495 from the 5' end.

[0171] In certain embodiments, modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 8 consecutive nucleobases that are complementary to a target region. In certain embodiments, modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 8 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2112, 2021-2134, 2022-2140, 2023-2151, 2024-2162, 2025-2173, 2026-2184, 2027-2195, 2028-2196, 2029-2207, 2030-2198, 2030-2199, 2040-2191, 2040-2199, 2050-2199, 2060-2191, 2070-2192, 2070-2194, 2070-2195, 2080-2196, 2090-2209, 2100- 3, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1325 24, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~148 Target positions 8, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region containing at least 8 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0172] In certain embodiments, modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 10 consecutive nucleobases that are complementary to a target region. In certain embodiments, modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 10 consecutive nucleobases that are complementary to a target region, and the target region is 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2111, 2020-2122, 2020-2133, 2020-2144, 2020-2155, 2020-2161, 2020-2172, 2020-2183, 2020-2194, 2020-2195, 2020-2196, 2020-2197, 2020-2198, 2020-2199, 2030-3040, 2030-3040, 2030-3050, 2030-3060, 2030-3070, 2030-3081, 2030-3090, 20 43, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1 324, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~14 Target positions 88, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region containing at least 10 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0173] In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 12 consecutive nucleobases that are complementary to a target region. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 12 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2111, 2020-2122, 2020-2133, 2020-2144, 2020-2155, 2020-2161, 2020-2172, 2020-2183, 2020-2194, 2020-2195, 2020-2196, 2020-2197, 2020-2198, 2020-2199, 2030-3040, 2030-3040, 2030-3050, 2030-3060, 2030-3070, 2030-3081, 2030-3090, 2 43, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1 324, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~14 Target positions 88, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region containing at least 12 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0174] In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 14 consecutive nucleobases that are complementary to a target region. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 14 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2112, 2021-2134, 2022-2140, 2023-2151, 2024-2162, 2025-2173, 2026-2184, 2027-2195, 2028-2196, 2029-2197, 2030-2199, 2040-2198, 2050-2199, 2060-2199, 2070-2199, 2080-2199, 2090-2200, 2100-2200, 2210-2210, 2220-2220, 2220-2230, 2 43, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1 324, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~14 Target positions 88, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region containing at least 14 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0175] In certain embodiments, the modified oligonucleotide is selected from the group consisting of 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-143, 128-144, 128-147, 232-245, 232-247, 233-246, 234-248, 235-249, 236-250, 237-251, 238-252, 239-253, 240-241, 242-254, 243-255, 244-256, 245-257, 246-258, 247-259, 250-260, 251-261, 252-262, 253-263, 254-264, 255-265, 256-266, 257-267, 258-268, 259-269, 260-270, 261-271, 262-272, 263-274, 264-275, 265-276, 266-277, 267-278, 268-279, 270-271, 271-272, 272-273, 273-274, 274-275, 275-276, 276-277, 277-278, 278-279, 280-281, 281-282, 3~247, 233~248, 234~247, 234~248, 1304~1323, 1306~1321, 1306~1324, 1307~1323, 1307~1324, 1307~1325, 1307~1326, 1308~1323, 1308~1324, 1308~1322, 1308~1325, 1309~1323, 1309~1 324, 1309-1325, 1309-1322, 1310-1323, 1310-1324, 1472-1485, 1472-1486, 1472-1487, 1472-1488, 1473-1487, 1473-1488, 1473-1489, 1474-1488, 1474-1489, 1475-1490, 1476-1490, 14 The modified oligonucleotide is a modified oligonucleotide comprising a nucleic acid base sequence complementary to an isometric portion of positions 76 to 1491, 1476 to 1495, 1477 to 1495, 1478 to 1496, 1479 to 1495, 1479 to 1496, 1479 to 1498, 1480 to 1494, 1480 to 1495, 1480 to 1496, 1480 to 1497, or 1480 to 1499. In certain embodiments, the modified oligonucleotide is a modified oligonucleotide comprising a nucleic acid base sequence complementary to an isometric portion of positions 128 to 143, 232 to 247, 233 to 248, 1309 to 1323, or 1480 to 1495 from the 5' end of the nucleic acid bases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing.

[0176] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide comprising a nucleic acid base sequence set forth in any one of SEQ ID NOs: 2 to 4, 7 to 64, 69 to 97, and 102 to 112 in the sequence listing. In certain embodiments, the modified oligonucleotide is a modified oligonucleotide comprising a nucleic acid base sequence set forth in any one of SEQ ID NOs: 2 to 4, 75, and 78 in the sequence listing.

[0177] In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of a nucleic acid base sequence set forth in any one of SEQ ID NOs: 2 to 4, 7 to 64, 69 to 97, and 102 to 112 in the sequence listing. In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of a nucleic acid base sequence set forth in any one of SEQ ID NOs: 2 to 4, 75, and 78 in the sequence listing.

[0178] In certain embodiments, the modified oligonucleotide has a nucleobase sequence comprising at least 8 consecutive nucleobases of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 75, or 78 of the Sequence Listing.

[0179] In certain embodiments, the modified oligonucleotide has a nucleobase sequence comprising at least 10 consecutive nucleobases of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 75, or 78 of the Sequence Listing.

[0180] In certain embodiments, the modified oligonucleotide has a nucleobase sequence comprising at least 12 contiguous nucleobases of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 75, or 78 of the Sequence Listing.

[0181] In certain embodiments, the modified oligonucleotide has a nucleobase sequence comprising at least 14 consecutive nucleobases of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 75, or 78 of the Sequence Listing.

[0182] In certain embodiments, the modified oligonucleotide has a nucleobase sequence comprising nucleobases consisting of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 75, or 78 of the Sequence Listing.

[0183] In certain embodiments, the modified oligonucleotide has a nucleobase sequence consisting of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 75, or 78 of the Sequence Listing.

[0184] In certain embodiments, the animal is a human.

[0185] In certain embodiments, administration comprises parenteral administration.

[0186] In certain embodiments, the compound is a single-stranded modified oligonucleotide.

[0187] In certain embodiments, the nucleobase sequence of a modified oligonucleotide is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to an equal length portion of any one of said regions of SEQ ID NO:1 of the Sequence Listing when measured across the entirety of the modified oligonucleotide. In certain embodiments, the nucleobase sequence of a modified oligonucleotide is 100% complementary to an equal length portion of any one of said regions of SEQ ID NO:1 of the Sequence Listing when measured across the entirety of the modified oligonucleotide.

[0188] In certain embodiments, at least one internucleoside linkage of the modified oligonucleotide is a modified internucleoside linkage, hi certain embodiments, each internucleoside linkage is a phosphorothioate internucleoside linkage.

[0189] In certain embodiments, at least one nucleoside of the modified oligonucleotide comprises a modified sugar. In certain embodiments, at least one modified sugar is a bicyclic sugar. In certain embodiments, at least one modified sugar is a 2'-O-methoxyethyl, 2'-O-methyl and / or 4'-(CH2) n Contains an -O-2' bridge, where n is 1 or 2.

[0190] In certain embodiments, the sugar moiety of the modified oligonucleotide comprises at least one modified sugar that is a bicyclic sugar, hi certain embodiments, at least one modified sugar is LNA, GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz], and / or ALNA[Trz].

[0191] In certain embodiments, at least one nucleoside of the modified oligonucleotide comprises a modified nucleobase. In certain embodiments, the modified nucleobase is 5-methylcytosine.

[0192] In certain embodiments, the modified oligonucleotide is a gapmer and comprises: a) a gap segment comprised of linked deoxynucleosides; b) a 5' wing segment comprised of linked nucleosides; and c) a 3' wing segment comprised of linked nucleosides, wherein the gap segment is positioned between the 5' wing segment and the 3' wing segment, and each nucleoside of each wing segment comprises a modified sugar, such as a 2'-O-methyl modified sugar, a 2'-O-methoxyethyl modified sugar, or a bicyclic sugar.

[0193] In certain embodiments, the modified oligonucleotide is a gapmer and comprises: a) a gap segment, which is a nucleoside comprising one or two nucleosides comprising a modified sugar, such as a 2'-O-methyl or a 2'-O-methoxyethyl modified sugar, and otherwise no modified sugars; b) a 5' wing segment comprising linked nucleosides; and c) a 3' wing segment comprising linked nucleosides. The gap segment is positioned between the 5' wing segment and the 3' wing segment, and each nucleoside of each wing segment comprises a modified sugar, such as a 2'-O-methyl modified sugar, a 2'-O-methoxyethyl sugar, or a bicyclic sugar.

[0194] In certain embodiments, the modified oligonucleotide is a gapmer and comprises: a) a gap segment having 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16 nucleosides that are either the only nucleosides with no modified sugar or that contain one or two nucleosides that contain a modified sugar, such as a 2'-O-methyl or a 2'-O-methoxyethyl modified sugar, and the rest of the nucleosides without modified sugars; b) a 5' wing segment having 2, 3, 4, 5, 6 or 7 nucleosides; and c) a 3' wing segment having 2, 3, 4, 5, 6, 7 or 8 nucleosides. wherein a gap segment is located between the 5' wing segment and the 3' wing segment, each nucleoside of each wing segment comprises a 2'-O-methyl modified sugar, a 2'-O-methoxyethyl sugar or a bicyclic sugar, each internucleoside linkage of the modified oligonucleotide comprises a phosphorothioate linkage, and some or all of the cytosines in the modified oligonucleotide may be 5'-methylcytosines.

[0195] In certain embodiments, the modified oligonucleotide is a gapmer and the number of nucleosides comprising the gapmer is 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30.

[0196] In certain embodiments, the modified oligonucleotide is a gapmer and contains 2'-O-methyl, 2'-O-methoxyethyl and / or 4'-(CH2) in the sugar portion of the nucleoside. n Contains an -O-2' bridge, where n is 1 or 2.

[0197] In certain embodiments, the modified oligonucleotide is a gapmer and comprises LNA, GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz], and / or ALNA[Trz] in the sugar portion of the nucleoside.

[0198] In certain embodiments, the modified oligonucleotide is a gapmer, which is a modified oligonucleotide consisting of 12 to 30 residues and has a nucleobase sequence comprising a modified oligonucleotide that is a nucleobase sequence comprising at least 8 consecutive nucleobases complementary to an equal-length portion of the nucleobases at positions 126 to 147, 232 to 248, 1306 to 1325, or 1472 to 1495 from the 5' end of the nucleobases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing. In certain embodiments, the modified oligonucleotide is a modified oligonucleotide consisting of 12 to 30 residues and has a nucleobase sequence comprising a modified oligonucleotide that is a nucleobase sequence comprising at least 9, 10, 11, or 12 consecutive nucleobases complementary to an equal-length portion of the nucleobases at positions 126 to 147, 232 to 248, 1306 to 1325, or 1472 to 1495 from the 5' end of the nucleobases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing.

[0199] In certain embodiments, the modified oligonucleotide is a gapmer, which is a nucleic acid base sequence that includes a sequence of at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 or 22 consecutive nucleic acid bases that are complementary to an equal length portion of the nucleic acid bases from positions 126 to 147 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0200] In certain embodiments, the modified oligonucleotide is a gapmer, which is a nucleobase sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, 16 or 17 consecutive nucleobases that are complementary to an equal length portion of the nucleobases at positions 232 to 248 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0201] In certain embodiments, the modified oligonucleotide is a gapmer, which is a nucleic acid base sequence that includes at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 consecutive nucleic acid bases that are complementary to an equal length portion of the nucleic acid bases from positions 1306 to 1325 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0202] In certain embodiments, the modified oligonucleotide is a gapmer, which is a nucleobase sequence comprising at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23 or 24 consecutive nucleobases that are complementary to an equal length portion of the nucleobases from positions 1472 to 1495 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO:1 in the Sequence Listing, and is a modified oligonucleotide of 30 residues or less.

[0203] In certain embodiments, the modified oligonucleotide is a gapmer of a modified oligonucleotide consisting of 12 to 30 residues, and comprises a nucleobase sequence that is complementary to an equal-length portion of the nucleobases from positions 126 to 147 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the equal-length portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0204] In certain embodiments, the modified oligonucleotide is a gapmer of a modified oligonucleotide consisting of 12 to 30 residues, and comprises a nucleobase sequence that is complementary to an equal-length portion of the nucleobases at positions 233 to 248 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the equal-length portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0205] In certain embodiments, the modified oligonucleotide is a gapmer of a modified oligonucleotide consisting of 12 to 30 residues, and comprises a nucleobase sequence that is complementary to an equal-length portion of the nucleobases from positions 1309 to 1323 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the equal-length portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0206] In certain embodiments, the modified oligonucleotide is a gapmer of a modified oligonucleotide consisting of 12 to 30 residues, and comprises a nucleobase sequence that is complementary to an isolength portion of the nucleobases from positions 1472 to 1495 from the 5' end of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the Sequence Listing in the isolength portion. In addition, in certain embodiments, the amino acid sequence may be 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues, 13 to 23 residues, 13 to 24 residues, 13 to 25 residues, 13 to 26 ... the modified oligonucleotide is 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues. In this case, the oligonucleotides contained in the 5' wing segment and / or the 3' wing segment contain at least one nucleoside containing at least one modified sugar selected from GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz] and ALNA[Trz], and may further contain a 2'-O-methoxyethyl modified sugar and / or a 2'-O-methyl modified sugar.

[0207] In certain embodiments, the modified oligonucleotide is a gapmer of a modified oligonucleotide consisting of 12 to 30 residues, and has a nucleobase sequence complementary to an isometric portion from positions 1480 to 1495 from the 5' end of the nucleobase of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing, and has a nucleobase sequence having a complementary base of the 1480th base from the 5' end of the nucleobase of SEQ ID NO: 1 at its 3' end, and is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to SEQ ID NO: 1 in the sequence listing in the isometric portion. In addition, in certain embodiments, 12 to 29 residues, 12 to 28 residues, 12 to 27 residues, 12 to 26 residues, 12 to 25 residues, 12 to 24 residues, 12 to 23 residues, 12 to 22 residues, 12 to 21 residues, 12 to 20 residues, 12 to 19 residues, 12 to 18 residues, 12 to 17 residues, 12 to 16 residues, 12 to 15 residues, 12 to 14 residues, 13 to 29 residues, 13 to 28 residues, 13 to 27 residues, 13 to 26 residues, 13 to 25 residues, 13 to 24 residues, 13 to 23 residues, 13 to 22 residues , 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, or 14 to 15 residues.

[0208] In certain embodiments, the modified oligonucleotides provided herein are gapmers and target any one of the following regions of SEQ ID NO:1 in the Sequence Listing: 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-143, 128-144, 128-147, 23 2~245, 232~247, 233~246, 233~247, 233~248, 234~247, 234~248, 1304~1323, 1306~1321, 1306~1324, 1307~1323, 1307~1324, 1307~1325, 1307~1326, 1308~1323, 1308~1324, 1308~132 2, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~1488, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein are gapmers and target any one of the following regions of SEQ ID NO:1 in the Sequence Listing: positions 128-143, 232-247, 233-248, 1309-1323 and 1480-1495 from the 5' end.

[0209] In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region that contains at least 8 consecutive nucleobases that are complementary to a target region. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 8 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2112, 2021-2134, 2022-2140, 2023-2151, 2024-2162, 2025-2173, 2026-2184, 2027-2195, 2028-2196, 2029-2207, 2030-2198, 2030-2199, 2040-2191, 2040-2199, 2050-2199, 2060-2191, 2070-2192, 2070-2194, 2070-2195, 2080-2196, 2090-2209 3, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1325 24, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~148 Target positions 8, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region containing at least 8 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0210] In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region that contains at least 10 consecutive nucleobases that are complementary to a target region. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 10 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2112, 2021-2134, 2022-2140, 2023-2151, 2024-2162, 2025-2173, 2026-2184, 2027-2195, 2028-2196, 2029-2207, 2030-2198, 2030-2199, 2040-2191, 2040-2199, 2050-2199, 2060-2191, 2070-2192, 2070-2194, 2070-2195, 2080-2196, 2090-22 43, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1 324, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~14 Target positions 88, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region containing at least 10 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0211] In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region that contains at least 12 consecutive nucleobases that are complementary to a target region. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 12 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-2101, 2020-2111, 2020-2122, 2020-2133, 2020-2144, 2020-2155, 2020-2161, 2020-2172, 2020-2183, 2020-2194, 2020-2195, 2020-2196, 2020-2197, 2020-2198, 2020-2199, 2030-3040, 2030-3040, 2030-3050, 2030-3060, 2030-3070, 2030-3081, 2030-30 43, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1 324, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~14 Target positions 88, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region containing at least 12 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0212] In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region that contains at least 14 consecutive nucleobases that are complementary to a target region. In certain embodiments, the modified oligonucleotides provided herein have a nucleobase sequence that includes a complementary region that contains at least 14 consecutive nucleobases that are complementary to a target region, the target region being 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-149, 129-200, 2010-2020, 2011-2020, 2012-2030, 2013-2040, 2014-2050, 2015-2060, 2016-2070, 2017-2080, 2018-2090, 2019-3010, 2020-3020, 2021-3030, 2022-3040, 2023-3050, 2024-3060, 2025-3070, 2026-3080, 2027-3090, 2028-3090, 2029-4010, 2030-4020, 2030-4040, 2030-4050, 2030-4060, 2040-4070, 2040-4080, 2050-4090, 2060-4090, 2070-4090, 2080-4090, 2090-50 43, 128-144, 128-147, 232-245, 232-247, 233-246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1 324, 1308~1322, 1308~1325, 1309~1323, 1309~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~14 Target positions 88, 1474-1489, 1475-1490, 1476-1490, 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497 or 1480-1499. In certain embodiments, the modified oligonucleotides provided herein are gapmers and have a nucleobase sequence that includes a complementary region containing at least 14 consecutive nucleobases that are complementary to a target region, the target region targeting positions 128-143, 232-247, 233-248, 1309-1323 or 1480-1495 from the 5' end of SEQ ID NO:1 in the Sequence Listing.

[0213] In certain embodiments, the modified oligonucleotide is a gapmer and is selected from the group consisting of 126-141, 126-143, 127-142, 127-143, 127-144, 127-146, 128-143, 128-144, 128-147, 232-245, 232-247, 233-248, 234-249, 235-250, 236-251, 237-252, 238-253, 239-260, 241-242, 242-263, 243-264, 244-265, 245-266, 246-267, 247-268, 248-269, 246, 233-247, 233-248, 234-247, 234-248, 1304-1323, 1306-1321, 1306-1324, 1307-1323, 1307-1324, 1307-1325, 1307-1326, 1308-1323, 1308-1324, 1308-1322, 1308-1325, 1309-1323, 13 09~1324, 1309~1325, 1309~1322, 1310~1323, 1310~1324, 1472~1485, 1472~1486, 1472~1487, 1472~1488, 1473~1487, 1473~1488, 1473~1489, 1474~1488, 1474~1489, 1475~1490, 1476~1490, The modified oligonucleotide is a modified oligonucleotide consisting of a nucleic acid base sequence complementary to an isometric portion of positions 1476-1491, 1476-1495, 1477-1495, 1478-1496, 1479-1495, 1479-1496, 1479-1498, 1480-1494, 1480-1495, 1480-1496, 1480-1497, or 1480-1499. In a certain embodiment, the modified oligonucleotide is a gapmer, and is a modified oligonucleotide consisting of a nucleic acid base sequence complementary to an isometric portion of positions 128-143, 232-247, 233-248, 1309-1323, or 1480-1495 from the 5' end of the nucleic acid bases of the mature mRNA of DUX4 of SEQ ID NO: 1 in the Sequence Listing.

[0214] In certain embodiments, the modified oligonucleotide is a gapmer, and is a modified oligonucleotide consisting of a nucleic acid base sequence set forth in any one of SEQ ID NOs: 2 to 4, 7 to 64, 69 to 97, and 102 to 112 in the sequence listing. In certain embodiments, the modified oligonucleotide is a gapmer, and is a modified oligonucleotide consisting of a nucleic acid base sequence set forth in any one of SEQ ID NOs: 2 to 4, 75, and 78 in the sequence listing.

[0215] In certain embodiments, the modified oligonucleotide is a gapmer and is a modified oligonucleotide set forth in any one of compound numbers 1-112, 114-132, and 137-246. In certain embodiments, the modified oligonucleotide is a gapmer and is a modified oligonucleotide set forth in any one of compound numbers 1-3, 123, 157, 204, 221, and 231.

[0216] In this specification, in symbols such as "Gls" representing nucleotides, the abbreviation shown in the left position refers to the nucleobase portion, the abbreviation shown in the center position refers to the sugar portion, and the abbreviation shown in the right position refers to the internucleoside bond type.

[0217] In certain embodiments, the modified oligonucleotide is a gapmer and has the following formula: GlsMlsMlsTdsAdsGdsAdsCdsAdsGdsCdsGdsTdsMlsGlsGl; A modified oligonucleotide represented by: During the ceremony Each nucleobase is represented by the following symbol: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: l=LNA, d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: s = phosphorothioate is a modified oligonucleotide,

[0218] In certain embodiments, the modified oligonucleotide is a gapmer, Below formula: GmsMmsMmsTdsAdsGdsAdsCdsAdsGdsCdsGdsTdsMmsGmsGm; A modified oligonucleotide represented by: During the ceremony, Each nucleobase is represented by the following symbol: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: m=ALNA[Ms], d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: s=phosphorothioate is a modified oligonucleotide indicated accordingly.

[0219] In certain embodiments, the modified oligonucleotide is a gapmer and has the following formula: GmsMmsAmsGdsTdsTdsCdsTdsCdsCdsGdsCdsGmsGmsTm; A modified oligonucleotide represented by: During the ceremony, The symbols for each nucleobase are as follows: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: m=ALNA[Ms], d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: s = phosphorothioate is a modified oligonucleotide,

[0220] In certain embodiments, the modified oligonucleotide is a gapmer and has the following formula: MlsGlsAlsGdsAdsTdsTdsCdsCdsCdsGdsCdsCdsGlsGlsTl; A modified oligonucleotide according to the formula: During the ceremony, Each nucleobase is represented by the following symbol: A=adenine, T=thymine, G=guanine, C=cytosine, M=5-methylcytosine, As indicated; Each sugar moiety has the following symbol: l=LNA, d=2'-deoxyribose, As indicated; Each internucleoside bond is represented by the following symbol: s=phosphorothioate, is a modified oligonucleotide,

[0221] Certain embodiments provide a method for reducing DUX4 mRNA and / or DUX4 protein levels (e.g., intramuscular levels) in an animal with a DUX4-associated disease, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4.

[0222] Certain embodiments provide methods of reducing DUX4 mRNA and / or DUX4 protein levels (e.g., intramuscular levels) in an animal with FSHD, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4. Certain embodiments also provide methods of reducing muscle impairment and / or improving motor function in an animal with FSHD, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4.

[0223] Certain embodiments provide a method for treating, ie, curing, preventing, ameliorating, or alleviating, FSHD, comprising administering to an animal an effective amount of a modified oligonucleotide against DUX4.

[0224] Certain embodiments provide a method for preventing, ameliorating, or alleviating various symptoms of FSHD (e.g., facial muscle weakness, ptosis, inability to whistle, reduced facial expression, depressed or angry facial expressions, difficulty pronouncing words, scapular muscle weakness (deformities such as winged scapula, rounded shoulders, etc.), lower limb weakness, hearing loss, and heart disease), comprising administering to an animal an effective amount of a modified oligonucleotide against DUX4.

[0225] Certain embodiments provide a method for reducing the level of mRNA and / or protein (e.g., in blood B cells) resulting from the fusion of the DUX4 gene with the IGH gene in an animal with, for example, B cell acute lymphoblastic leukemia, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4. Certain embodiments also provide a method for treating, i.e., curing, preventing, ameliorating, or alleviating, B cell acute lymphoblastic leukemia, for example, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4.

[0226] Certain embodiments provide a method of reducing the levels of mRNA and / or protein (e.g., levels within a sarcoma) resulting from a fusion of the DUX4 gene with a CIC gene in an animal, such as a differentiated round cell sarcoma, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4. Certain embodiments also provide a method of treating, i.e., curing, preventing, ameliorating, or ameliorating, a differentiated round cell sarcoma, such as a differentiated round cell sarcoma, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4.

[0227] Certain embodiments provide a method of reducing the level of mRNA and / or protein (e.g., in a sarcoma) resulting from a fusion of the DUX4 gene with the EWSR1 gene in an animal, such as embryonal rhabdomyosarcoma, comprising administering to the animal a modified oligonucleotide against DUX4. Certain embodiments also provide a method of treating, i.e., curing, preventing, ameliorating, or ameliorating, embryonal rhabdomyosarcoma, or the like, comprising administering to the animal an effective amount of a modified oligonucleotide against DUX4.

[0228] Certain embodiments provide a method for treating, preventing, improving, or alleviating DUX4-related diseases with fewer side effects, comprising administering a modified oligonucleotide against DUX4 to an animal. In certain embodiments, the side effects include injection site reactions, abnormal liver function tests, abnormal kidney function, liver toxicity (abnormal histopathological findings: hepatocyte degeneration and necrosis, hepatocyte hypertrophy, etc.), nephrotoxicity (abnormal histopathological findings, etc.), central nervous system abnormalities, myopathy, and fatigue. For example, elevated levels of ALT, AST, γ-GTP, GLDH, ALP (alkaline phosphatase), or TBA (total bile acids) in the blood may indicate liver toxicity or liver dysfunction. For example, elevated bilirubin may indicate liver toxicity or liver dysfunction. Also, elevated urinary protein, elevated creatinine in the blood, or elevated UN may indicate nephrotoxicity or kidney dysfunction.

[0229] Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for use in any of the therapeutic methods described herein. For example, certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for treating, i.e., treating, preventing, delaying, or ameliorating, FSHD. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for inhibiting the expression of DUX4 and treating, i.e., treating, preventing, delaying, or ameliorating, DUX4-related disease and / or its symptoms. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for reducing the expression of DUX4 in an animal. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for reducing myotonia, preferentially reducing the level (e.g., intramuscular level) of DUX4-FL mRNA in an animal. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for treating an animal with FSHD. Certain embodiments provide for the use of a compound described herein or a pharmaceutical composition containing the compound in the manufacture of a medicament for treating one or more symptoms and outcomes associated with the development of FSHD, including muscle rigidity, myotonia, facial muscle weakness, ptosis, inability to whistle, reduced facial expression changes, depressed or angry facial expressions, difficulty in pronouncing words, scapular muscle weakness (deformities such as winged scapula, hunched shoulders, etc.), lower limb weakness, hearing loss, and heart disease. Certain embodiments provide for the use of a compound described herein or a pharmaceutical composition containing the compound in the manufacture of a medicament for preventing the expression of DUX4 protein by inducing transcription of the DUX4 gene, translation of DUX4 mRNA, and cleavage of DUX4 mRNA.

[0230] Certain embodiments provide kits for treating, i.e., treating, preventing, or ameliorating FSHD as described herein, comprising a) a compound described herein, and optionally b) an additional agent or therapy described herein. The kit may further comprise instructions or a label for using the kit to treat, i.e., treat, prevent, or ameliorate FSHD.

[0231] Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for use in any of the therapeutic methods described herein. For example, certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for treating, i.e., treating, ameliorating, or preventing FSHD. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for inhibiting the expression of DUX4 and treating, i.e., treating, preventing, delaying, or ameliorating DUX4-related diseases and / or symptoms thereof. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for reducing the expression of DUX4 in an animal. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for reducing myotonia, preferentially reducing the level (e.g., intramuscular level) of DUX4-FL mRNA in an animal. Certain embodiments provide for the use of any of the compounds described herein or pharmaceutical compositions containing the compounds in the manufacture of a medicament for treating an animal with FSHD. Certain embodiments provide a compound described herein or a pharmaceutical composition containing the compound for treating one or more symptoms and outcomes associated with the development of FSHD, including muscle rigidity, myotonia, facial muscle weakness, ptosis, inability to whistle, reduced facial expression changes, depressed or angry facial expressions, difficulty pronouncing words, scapular muscle weakness (deformities such as winged scapula, bowed shoulders, etc.), lower limb weakness, hearing loss, and heart disease. Certain embodiments provide a modified oligonucleotide having a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NOs: 2-4, 7-64, 69-97, or 102-112 of the Sequence Listing, or a compound of Compound Nos. 1-112, 114-132, or 137-246.

[0232] In certain embodiments, a modified oligonucleotide has a nucleobase sequence that, when written in the 5' to 3' direction, comprises the reverse complement of a target segment of a target nucleic acid to which it is targeted. In certain such embodiments, a modified oligonucleotide has a nucleobase sequence that, when written in the 5' to 3' direction, comprises the reverse complement of a target segment of a target nucleic acid to which it is targeted.

[0233] In certain embodiments, the modified oligonucleotides described herein that target DUX4 are 12-30 nucleotides in length. In other words, in some embodiments, the modified oligonucleotides are 12-30 linked nucleobase residues. In other embodiments, the modified oligonucleotides are 12-29 residues, 12-28 residues, 12-27 residues, 12-26 residues, 12-25 residues, 12-24 residues, 12-23 residues, 12-22 residues, 12-21 residues, 12-20 residues, 12-19 residues, 12-18 residues, 12-17 residues, 12-16 residues, 12-15 residues, 12-14 residues, 13-29 residues, 13-28 residues, 13-27 residues, 13-26 residues, 13-25 residues, 13-24 residues, 13-23 residues, 13-22 residues, or 13-29 residues. and modified oligonucleotides comprising linked nucleobases of 13 to 21 residues, 13 to 20 residues, 13 to 19 residues, 13 to 18 residues, 13 to 17 residues, 13 to 16 residues, 13 to 15 residues, 13 to 14 residues, 14 to 29 residues, 14 to 28 residues, 14 to 27 residues, 14 to 26 residues, 14 to 25 residues, 14 to 24 residues, 14 to 23 residues, 14 to 22 residues, 14 to 21 residues, 14 to 20 residues, 14 to 19 residues, 14 to 18 residues, 14 to 17 residues, 14 to 16 residues, and 14 to 15 residues. In certain such embodiments, modified oligonucleotides comprise modified oligonucleotides of lengths of 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30 linked nucleobases, or a range defined by any two of the above values. In certain embodiments, modified oligonucleotides of any of these lengths comprise at least 8 contiguous nucleobases of a nucleobase sequence set forth in any one of SEQ ID NOs: 2-4, 7-64, 69-97 or 102-112 of the Sequence Listing, of at least 8, at least 9, at least 10, at least 11, at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18 or at least 19 contiguous nucleobases of any of the nucleobase sequences of the exemplary modified oligonucleotides described herein.

[0234] The length of antisense compounds, such as antisense oligonucleotides, can be increased or decreased and / or mismatched bases can be introduced without losing activity. For example, Woolf et al. (Proc. Natl. Acad. Sci. USA 89:7305-7309, 1992) tested a series of antisense oligonucleotides, 13-25 nucleobases long, for their ability to induce cleavage of target RNA in an oocyte injection model, and reported that 25 nucleobases long antisense oligonucleotides with 8 or 11 mismatched bases near the ends of the antisense oligonucleotides can induce specific cleavage of target mRNA, albeit to a lesser extent than antisense oligonucleotides without mismatches. Similarly, target-specific cleavage has been reported to be achieved using 13 nucleobases long antisense oligonucleotides, including those with 1 or 3 mismatches.

[0235] Gautschi et al. (J. Natl. Cancer Inst. 93:463-471, March 2001) reported that an oligonucleotide with 100% complementarity to bcl-2 mRNA and three mismatches to bcl-xL mRNA exhibited the ability to reduce the expression of both bcl-2 and bcl-xL in vitro and in vivo. Furthermore, it was reported that this oligonucleotide exhibited potent antitumor activity in vivo.

[0236] Target Nucleic Acids, Target Regions and Nucleotide Sequences Nucleotide sequences encoding DUX4 include, but are not limited to, the following sequences: The sequence set forth in GenBank Accession No. NM_001293798.2, incorporated herein as SEQ ID NO: 1 of the Sequence Listing. The splice variant of SEQ ID NO: 1 of the Sequence Listing is also referred to as DUX4-FL1 or the mature mRNA of DUX4. The sequence set forth in GenBank Accession No. NM_001306068.2 (herein incorporated as SEQ ID NO: 5 of the Sequence Listing). The splice variant of SEQ ID NO: 5 of the Sequence Listing is also referred to as DUX4-FL2. The sequence set forth in GenBank Accession No. NM_001363820.1 (herein incorporated as SEQ ID NO: 6 in the Sequence Listing). The splicing variant of SEQ ID NO: 6 in the Sequence Listing is also called DUX4-s. -SNPs of each of the above splicing variants. The sequences described in each SEQ ID NO of the sequence listing of the examples included herein are independent of any modifications to the sugar moiety, internucleoside bond or nucleobase.Therefore, the modified oligonucleotides defined by the SEQ ID NO of the sequence listing can independently contain one or more modifications to the sugar moiety, internucleoside bond or nucleobase.The modified oligonucleotides described by compound numbers represent combinations of nucleobase sequences and motifs.

[0237] In certain embodiments, the target region is a structurally defined region of the target nucleic acid.For example, the target region can include one or more of 3'UTR, 5'UTR, exon, intron, exon / intron junction, coding region, translation initiation region, translation termination region or other defined nucleic acid region.The structurally defined region for DUX4 can be obtained by accession number from sequence database such as NCBI, and such information is incorporated herein by reference.In certain embodiments, the target region can include the sequence from the 5' target site of one target segment within the target region to the 3' target site of another target segment within the target region.

[0238] Targeting involves determining at least one target segment to which the modified oligonucleotide hybridizes, resulting in a desired effect. In certain embodiments, the desired effect is a reduction in mRNA target nucleic acid levels. In certain embodiments, the desired effect is a reduction in the levels of a protein encoded by the target nucleic acid, or a change in a phenotype associated with the target nucleic acid.

[0239] A target region may include one or more target segments. Multiple target segments within a target region may overlap. Alternatively, they may not overlap. In certain embodiments, target segments within a target region are separated by about 300 or less nucleotides. In certain embodiments, target segments within a target region are separated by a number of nucleotides that are 250, 200, 150, 100, 90, 80, 70, 60, 50, 40, 30, 20, or 10 nucleotides of the target nucleic acid, or are about, or are less than, these number of nucleotides, or are a range defined by any two of the aforementioned values. In certain embodiments, target segments within a target region are separated by 5 or less, or about 5 or less nucleotides of the target nucleic acid. In certain embodiments, the target segments are contiguous. Target regions defined by a range are contemplated that have a starting nucleic acid that is any of the 5' target sites or 3' target sites listed herein.

[0240] Suitable target segments can be found in 5'UTR, coding region, 3'UTR, intron, exon or exon / intron junction. Suitable target segments also include start codons or stop codons. Suitable target segments can specifically exclude certain structurally defined regions, such as start codons or stop codons.

[0241] The determination of suitable target segments can include comparing the sequence of target nucleic acid with other sequences throughout the genome.For example, the BLAST algorithm can be used to identify similar regions between different nucleic acids.This comparison can prevent the selection of modified oligonucleotide sequences that can hybridize in a non-specific manner to sequences other than the selected target nucleic acid (i.e., non-target sequences or off-target sequences).

[0242] There may be variation in activity (e.g., as determined by percent reduction in target nucleic acid level) of modified oligonucleotides within the active target region. In certain embodiments, reduction in DUX4 mRNA levels is indicative of inhibition of DUX4 protein expression. Reduction in DUX4 protein levels is also indicative of inhibition of target mRNA expression. Furthermore, phenotypic changes, such as reducing myotonia and reducing myopathy, may be indicative of inhibition of DUX4 mRNA and / or protein expression.

[0243] Hybridization In some embodiments, hybridization occurs between the modified oligonucleotides disclosed herein and DUX4 nucleic acid. The most common mechanism of hybridization involves hydrogen bonding (e.g., Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding) between complementary nucleic acid bases of nucleic acid molecules. The strength of hybridization can be expressed as melting temperature Tm. Tm is the temperature at which 50% of hybridized double-stranded nucleic acid dissociates into single-stranded nucleic acid, and varies depending on the salt conditions of the solution, the length and base sequence of the nucleic acid, etc., but the higher the Tm value, the stronger the hybridization.

[0244] Hybridization occurs under a variety of conditions. Stringent conditions are sequence-dependent and are determined by the nature and composition of the nucleic acid molecules to be hybridized.

[0245] Methods for determining whether a sequence is specifically hybridizable to a target nucleic acid are well known in the art (Sambrooke and Russell, Molecular Cloning: A Laboratory Manual, 3rd Ed., 2001). In certain embodiments, the modified oligonucleotides provided herein are specifically hybridizable to DUX4 nucleic acids.

[0246] Complementarity A modified oligonucleotide and a target nucleic acid are complementary to one another when a sufficient number of nucleobases of the modified oligonucleotide are capable of hydrogen bonding with corresponding nucleobases of the target nucleic acid such that a desired effect occurs (e.g., antisense inhibition of a target nucleic acid, such as a DUX4 nucleic acid).

[0247] The modified oligonucleotides can hybridize across one or more segments of a DUX4 nucleic acid such that intervening or adjacent segments are not involved in the hybridization event (eg, loop structures, mismatches or hairpin structures).

[0248] In certain embodiments, the modified oligonucleotides provided herein, or specified portions thereof, are 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% complementary to a DUX4 nucleic acid, target region, target segment or specified portions thereof. In certain embodiments, the modified oligonucleotide is at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% complementary to a DUX4 nucleic acid, target region, target segment or a specified portion thereof, and comprises at least 8, at least 9, at least 10, at least 11, at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18 or at least 19 consecutive nucleobases of the nucleobase sequence of any of the exemplary modified oligonucleotides described herein (e.g., at least 8 consecutive nucleobases of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 7-64, 69-97 or 102-112 of the Sequence Listing). The percent complementarity of the modified oligonucleotide with the target nucleic acid can be determined using routine methods and is measured throughout the entire modified oligonucleotide.

[0249] For example, a modified oligonucleotide in which 18 of 20 nucleobases of the modified oligonucleotide are complementary to a target region and therefore will specifically hybridize corresponds to 90 percent complementarity. In this example, the remaining non-complementary nucleobases can be clustered or flanked by complementary nucleobases, and do not have to be contiguous with each other or with complementary nucleobases. The percent complementarity of a modified oligonucleotide with a target nucleic acid region can be routinely determined using BLAST (basic local alignment search tools) and PowerBLAST programs (Altschulet et al., J. Mol. Biol., 1990, 215, 403410; Zhang and Madden, Genome Res., 1997, 7, 649656) known in the art. Percent homology, sequence identity or complementarity can be determined, for example, by the GAP program (Wisconsin Sequence Analysis Package, Version 8 for Unix, Genetics Computer Group, University Research Park, Madison Wis.) using default settings using the algorithm of Smith and Waterman (Adv. Appl. Math., 1981, 2, 482 489).

[0250] The site of the non-complementary nucleobase may be at the 5'-end or 3'-end of the modified oligonucleotide. Alternatively, the non-complementary nucleobase(s) may be at an internal position of the modified oligonucleotide. When two or more non-complementary nucleobases are present, they may be contiguous (i.e. linked) or non-contiguous. In one embodiment, the non-complementary nucleobase is located in the wing segment of a gapmer modified oligonucleotide.

[0251] In certain embodiments, modified oligonucleotides that are, or are up to 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30 nucleobases in length contain no more than 3, no more than 2 or no more than 1 non-complementary nucleobase(s) to a target nucleic acid, e.g., a DUX4 nucleic acid or a specified portion thereof.

[0252] Modified oligonucleotides provided herein also include those that are complementary to a portion of a target nucleic acid. As used herein, a "portion" refers to a defined number of consecutive (i.e. linked) nucleobases within a region or segment of a target nucleic acid. A "portion" can also refer to a defined number of consecutive nucleobases of a modified oligonucleotide. In certain embodiments, the modified oligonucleotide is complementary to at least an 8 nucleobase portion of a target segment. In certain embodiments, the modified oligonucleotide is complementary to at least a 10 nucleobase portion of a target segment. In certain embodiments, the modified oligonucleotide is complementary to at least a 15 nucleobase portion of a target segment. Modified oligonucleotides that are complementary to at least an 8, at least an 9, at least an 10, at least an 11, at least an 12, at least an 13, at least an 14, at least an 15, at least an 16, at least an 17, at least an 18, at least an 19, at least an 20 or more nucleobase portion of a target segment, or a range defined by any two of these values, are also contemplated.

[0253] identity The modified oligonucleotides provided herein can also have a specified percent identity to a compound or part thereof represented by a specific nucleotide sequence, a sequence number in the sequence listing, or a specific compound number.As used herein, a modified oligonucleotide is identical to a sequence disclosed herein if it has the same nucleic acid base pairing ability.For example, an RNA containing uracil instead of thymidine in a disclosed DNA sequence is considered to be identical to the DNA sequence, since both uracil and thymidine pair with adenine.Shortened and extended versions of the modified oligonucleotides described herein and compounds with non-identical bases to the modified oligonucleotides provided herein are also contemplated.The non-identical bases may be adjacent to each other or distributed throughout the modified oligonucleotide.The percent identity of a modified oligonucleotide is calculated according to the number of bases that have the same base pairing to the sequence being compared.

[0254] In certain embodiments, the modified oligonucleotide or portion thereof is at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical to one or more of the exemplary modified oligonucleotides disclosed herein or the SEQ ID NOs in the Sequence Listing or portions thereof.

[0255] qualification A nucleoside is a base-sugar combination. The nucleobase (also known as base) portion of a nucleoside is usually a heterocyclic base moiety. A nucleotide is a nucleoside that further comprises a phosphate group covalently linked to the sugar portion of the nucleoside. For nucleosides that contain a pentofuranosyl sugar, the phosphate group can be linked to the 2', 3' or 5' hydroxyl portion of the sugar. Oligonucleotides are formed through the covalent linkage of adjacent nucleosides to each other to form a linear polymeric oligonucleotide. Within the oligonucleotide structure, the phosphate groups are commonly referred to as forming the internucleoside linkages of the oligonucleotide.

[0256] Modifications in modified oligonucleotides include substitutions or changes to internucleoside linkages, sugar moieties, or nucleobases. Modified oligonucleotides are often preferred over natural forms due to desirable properties such as, for example, enhanced cellular uptake, enhanced affinity for nucleic acid targets, increased stability in the presence of nucleases, or increased inhibitory activity.

[0257] Modified Internucleoside Linkages The naturally occurring internucleoside linkage of RNA and DNA is a 3'-5' phosphodiester linkage. Modified oligonucleotides having one or more modified, i.e., non-naturally occurring, internucleoside linkages are often selected over modified oligonucleotides having naturally occurring internucleoside linkages due to desirable properties such as, for example, enhanced cellular uptake, enhanced affinity for target nucleic acids, and increased stability in the presence of nucleases.

[0258] The oligonucleotide with modified internucleoside linkage includes the internucleoside linkage that holds phosphorus atom and the internucleoside linkage that does not have phosphorus atom.Exemplary phosphorus-containing internucleoside linkages include, but are not limited to, one or more of phosphodiester, phosphotriester, methylphosphonate, phosphoramidate and phosphorothioate.Methods for preparing phosphorus-containing and non-phosphorus-containing linkages are well known.

[0259] In certain embodiments, the modified oligonucleotide targeted to DUX4 nucleic acid comprises one or more modified internucleoside linkages. In certain embodiments, the modified internucleoside linkages are phosphorothioate linkages. In certain embodiments, each internucleoside linkage of the modified oligonucleotide is a phosphorothioate internucleoside linkage.

[0260] modified sugar moiety The modified oligonucleotide of the present invention preferably has at least one nucleoside that comprises a modified sugar. In the present invention, the modified sugar refers to a modified sugar moiety, and modified oligonucleotides that contain one or more modified sugars have advantageous characteristics such as enhanced nuclease stability and increased binding affinity. At least one of the modified sugars preferably has a bicyclic sugar or substituted sugar moiety.

[0261] Examples of nucleosides having modified sugars include, but are not limited to, nucleosides containing 5'-vinyl, 5'-methyl (R or S), 4'-S, 2'-F, 2'-OCH3, 2'-OCH2CH3, 2'-OCH2CH2F, and 2'-O(CH2)2OCH3 substituents. Substituents at the 2' position include allyl, amino, azido, thio, O-allyl, O-C1-C2 10 Alkyl, OCF3, OCH2F, O(CH2)2SCH3, O(CH2)2-ON(R m )(R n ), O-CH2-C(=O)-N(R m )(R n ) and O-CH2-C(=O)-N(R l )-(CH2)2-N(R m )(R n )(In the formula, each R l , R m and R n are independently H or substituted or unsubstituted C1-C 10 It may also be selected from the group consisting of alkyl.

[0262] Examples of nucleosides having a bicyclic sugar include, but are not limited to, nucleosides comprising a bridge between the 4' and 2' ribosyl ring atoms. In certain embodiments, the oligonucleotides provided herein comprise nucleosides having one or more bicyclic sugars, where the bridge comprises one of the following formulas: 4'-(CH2)-O-2' (LNA); 4'-(CH2)-S-2'; 4'-(CH2)2-O-2' (ENA); 4'-CH(CH3)-O-2' and 4'-CH(CHOCH3)-O-2' (and analogs thereof, see U.S. Patent No. 7,399,845); 4'-C(CH3)(CH3)-O-2' (and analogs thereof, see WO 2009 / 0 06478); 4'-CH2-N(OCH3)-2' (and analogs thereof, see WO 2008 / 150729); 4'-CH2-ON(CH3)-2' (and analogs thereof, see US 2004-0171570); 4'-CH2-N(R)-O-2' (wherein R is H, C1-C12 alkyl or a protecting group) (see U.S. Patent No. 7,427,672); 4'-CH2-C(H)(CH3)-2' (and analogs thereof, see Chattopadhyaya et al., J. Org. Chem., 2009, 74, 118-134); and 4'-CH2-C(═CH2)-2' (and analogs thereof, see WO 2008 / 154401).

[0263] Nucleosides with additional bicyclic sugars have been reported in the published literature (e.g.: Srivastava et al., J. Am. Chem. Soc., 2007, 129(26)8362-8379; Friedene et al., Nucleic Acids Research, 2003, 21, 6365-6372; Elayadie et al., Curr. Opinion Invens. Drugs, 2001, 2, 558-561; Braasch et al., Chem. Biol., 2001, 8, 1-7; Orum et al., Curr. Opinion Mol. Ther., 2001, 3, 239-243; Wahlestedt et al., Proc. Natl. Acad. Sci. USA, 2000, 97, 5633-5638; Singh et al., al., Chem. Commun., 1998, 4, 455-456; Koshkin et al., Tetrahedron, 1998, 54, 3607-3630; Kumaret al., Bioorg. Med. Chem. Lett., 1998, 8, 2219-2222; Singhet al.,; US Patents US7,399,845;6,770,748;6,525,191;6,268,490; US2008-0039618; US2007-0287831; US2004-0171570; US2009-0012281; WO2010 / 036698; WO (See WO 2009 / 067647; WO 2009 / 067647; WO 2007 / 134181; WO 2005 / 021570; WO 2004 / 106356; WO 94 / 14226; WO 2009 / 006478; WO 2008 / 154401; and WO 2008 / 150729.) Each of the foregoing bicyclic sugar-containing nucleosides can be prepared with one or more stereochemical sugar configurations, including, for example, α-L-ribofuranose and β-D-ribofuranose.

[0264] The nucleoside GuNA, which has a bicyclic sugar, has been reported as an artificial nucleoside with a guanidine bridge (see WO2014 / 046212, WO2017 / 047816). The bicyclic nucleosides ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Trz] and ALNA[Oxz] have been reported as bridged artificial nucleic acid amino LNA (ALNA) (see Japanese Patent Application No. 2018-212424).

[0265] In certain embodiments, nucleosides having a bicyclic sugar include a bridge between the 4' and 2' carbon atoms of the pentofuranosyl sugar moiety, including but not limited to, -[C(R a )(R b )] n -, -C(R a )=C(R b )-, -C(R a )=N-, -C(=NR a )-, -C(=O)-, -C(=S)-, -N(R a )-, -O-, -Si(R a )2- and -S(=O) x -, where X is 0, 1 or 2; n is 1, 2, 3 or 4; and each R a and R b are independently H, a protecting group, hydroxyl, C1-C 12 Alkyl, substituted C1-C 12 Alkyl, C2-C 12 Alkenyl, substituted C2-C 12 Alkenyl, C2-C 12 Alkynyl, substituted C2-C 12 alkynyl, aromatic ring group, substituted aromatic ring group, heterocyclic group, substituted heterocyclic group, C5-C7 alicyclic group, substituted C5-C7 alicyclic group, halogen, OJ1, NJ1J2, SJ1, N3, COOJ1, acyl (C(=O)-H), substituted acyl, CN, sulfonyl (S(=O)2-J1) or sulfoxyl (S(=O)-J1); Each J1 and J2 is independently H, C1 to C 12 Alkyl, substituted C1-C 12Alkyl, C2-C 12 Alkenyl, substituted C2-C 12 Alkenyl, C2-C 12 Alkynyl, substituted C2-C 12 Alkynyl, aromatic ring group, substituted aromatic ring group, acyl (C(=O)-H), substituted acyl, heterocyclic group, substituted heterocyclic group, C1-C 12 Aminoalkyl, substituted C1-C 12 It is an aminoalkyl or a protecting group.

[0266] In certain embodiments, the bridge of the bicyclic sugar moiety is -[C(R a )(R b )] n -,-[C(R a )(R b )] n -O-, -C(R a R b )-N(R)-O- or -C(R a R b In certain embodiments, the bridges are 4'-CH2-2', 4'-(CH2)2-2', 4'-(CH2)3-2', 4'-CH2-O-2' (nucleosides having bicyclic sugars in this case are also referred to as LNAs), 4'-(CH2)2-O-2', 4'-CH2-ON(R)-2', and 4'-CH2-N(R)-O-2'-, where each R is independently H, a protecting group, or a C1-C 12 It is an alkyl.

[0267] In certain embodiments, the bridge of the bicyclic sugar moiety is 4'-CH2-O-2'-(LNA) or -CH2-N(R)-, where each R is independently -SO2-CH3 (ALNA[Ms]), -CO-NH-CH3 (ALNA[mU]), 1,5-dimethyl-1,2,4-triazol-3-yl (ALNA[Trz]), -CO-NH-CH(CH3)2 (ALNA[ipU]), 5-methyl-1,2,4-oxadiazol-3-yl (ALNA[Oxz]) (Japanese Patent Application No. 2018-212424).

[0268] In certain embodiments, nucleosides having bicyclic sugars are further defined by their isomeric configuration. For example, nucleosides containing a 4'-(CH2)-O-2' bridge can exist in either the α-L- or β-D-configuration.

[0269] In certain embodiments, nucleosides having a bicyclic sugar include those having a 4'-2' bridge, including, but not limited to, α-L-4'-(CH)-O-2', β-D-4'-CH-O-2', 4'-(CH)-O-2', 4'-CH-ON(R)-2', 4'-CH-N(R)-O-2', 4'-CH(CH)-O-2', 4'-CH-S-2', 4'-CH-CH(CH)-2', and 4'-(CH)-2', where R is H, a protecting group, C1-C2 12 Alkyl, or C1-C 12 and optionally alkyl-substituted urea or guanidine.

[0270] In certain embodiments, a nucleoside having a bicyclic sugar has the formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T a and T b are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, or the like; Z a is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, substituted C1-C6 alkyl, substituted C2-C6 alkenyl, substituted C2-C6 alkynyl, acyl, substituted acyl, substituted amide, thiol or substituted thiol.

[0271] In certain embodiments, each of the substituents is independently selected from halogen, oxo, hydroxyl, OJ, c , N.J. c Jd , S.J. c , N3, OC(=X)J c and N.J. e C(=X)NJ c J d (In the formula, each J c , J d and J e are independently H, C1-C6 alkyl or substituted C1-C6 alkyl, and X is O or NJ c The group is mono- or polysubstituted with substituents independently selected from:

[0272] In certain embodiments, a nucleoside having a bicyclic sugar has the formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T a and T b are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, or the like; Z b is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, substituted C1-C6 alkyl, substituted C2-C6 alkenyl, substituted C2-C6 alkynyl or substituted acyl (C(=O)-).

[0273] In certain embodiments, a nucleoside having a bicyclic sugar has the formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T a and T b are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, or the like; R dis C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, C2-C6 alkynyl or substituted C2-C6 alkynyl; each q a , q b , q c and q d are independently H, halogen, C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, C2-C6 alkynyl or substituted C2-C6 alkynyl, C1-C6 alkoxyl, substituted C1-C6 alkoxyl, acyl, substituted acyl, C1-C6 aminoalkyl or substituted C1-C6 aminoalkyl.

[0274] In certain embodiments, a nucleoside having a bicyclic sugar has the formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T a and T b are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, or the like; q a , q b , q e and q f are each independently hydrogen, halogen, C1-C 12 Alkyl, substituted C1-C 12 Alkyl, C2-C 12 Alkenyl, substituted C2-C 12 Alkenyl, C2-C 12 Alkynyl, substituted C2-C 12 Alkynyl, C1-C 12 Alkoxy, substituted C1-C 12 Alkoxy, O.J. j , S.J. j , S.O.J. j , SO2J j , N.J. j J k , N3, CN, C(=O)OJj, C(=O)NJj J k , C(=O)J j ,OC(=O)NJ j J k , N(H)C(=NH)NJ j J k , N(H)C(=O)-NJ j J k Or N(H)C(=S)NJ j J k and; Or, q e and q f Both are =C(q g )(q h ) and; q g and q h are each independently H, halogen, or C1-C 12 Alkyl or substituted C1-C 12 It is an alkyl.

[0275] The synthesis and preparation of adenine, cytosine, guanine, 5-methyl-cytosine, thymine and uracil bicyclic nucleosides (also called LNAs) with 4'-CH2-O-2' bridges have been described along with their oligomerization and nucleic acid recognition properties (Koshkin et al., Tetrahedron, 1998, 54, 3607-3630). The synthesis of nucleosides with bicyclic sugars has also been described in WO98 / 39352 and WO99 / 14226.

[0276] Various bicyclic nucleoside analogues with 4'-2' bridging groups such as 4'-CH2-O-2' (bicyclic nucleosides in this case are also called LNA) and 4'-CH2-S-2' have also been prepared (Kumaret et al., Bioorg. Med. Chem. Lett., 1998, 8, 2219-2222). Preparation of oligodeoxyribonucleotide duplexes containing bicyclic nucleosides for use as substrates for nucleic acid polymerases has also been described (Wengelet et al., WO99 / 14226). Furthermore, synthesis of 2'-amino-BNA (bicyclic nucleosides in this case are also called ALNA), i.e., conformationally restricted high affinity oligonucleotide analogues, has been described in the art (Singhet al., J. Org. Chem., 1998, 63, 10035-10039). Additionally, 2'-amino- and 2'-methylamino-BNAs have been prepared and the thermal stability of duplexes with complementary RNA and DNA strands has been previously reported.

[0277] In certain embodiments, a nucleoside having a bicyclic sugar has the formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T a and T b are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, or the like; each q i , q j , q k and q l are independently H, halogen, C1-C 12 Alkyl, substituted C1-C 12 Alkyl, C2-C 12 Alkenyl, substituted C2-C 12 Alkenyl, C2-C 12 Alkynyl, substituted C2-C 12 Alkynyl, C1-C 12 Alkoxyl, substituted C1-C 12 Alkoxyl, OJj , S.J. j , S.O.J. j , SO2J j , N.J. j J k , N3, CN, C(=O)OJ j , C(=O)NJ j J k , C(=O)J j ,OC(=O)NJ j J k , N(H)C(=NH)NJ j J k , N(H)C(=O)NJ j J k or N(H)C(=S)NJ j J k and; q i and q j or q l and q k Both are =C(q g )(q h ) in which q g and q h are each independently H, halogen, or C1-C 12 Alkyl or substituted C1-C 12 It is an alkyl.

[0278] One carbocyclic bicyclic nucleoside with a 4'-(CH2)3-2' bridge and an alkenyl analog bridge 4'-CH=CH-CH2-2' has been described (Frier et al., Nucleic Acids Research, 1997, 25(22), 4429-4443 and Albaek et al., J. Org. Chem., 2006, 71, 7731-7740). The synthesis and preparation of carbocyclic bicyclic nucleosides have also been described along with their oligomerization and biochemical studies (Srivastava et al., J. Am. Chem. Soc. 2007, 129(26), 8362-8379).

[0279] In certain embodiments, nucleosides having a bicyclic sugar include, but are not limited to, those shown below: (A) α-L-methyleneoxy (4'-CH2-O-2') BNA, (B) β-D-methyleneoxy (4'-CH2-O-2') BNA, (C) Ethyleneoxy (4'-(CH2)2-O-2') BNA, (D) aminooxy (4'-CH2-ON(R)-2') BNA; (E) oxyamino (4'-CH2-N(R)-O-2') BNA, (F) Methyl(methyleneoxy) (4'-CH(CH3)-O-2') BNA (also known as constrained ethyl or cEt); (G) methylene-thio(4'-CH2-S-2') BNA, (H) methylene-amino (4'-CH2-N(R)-2') BNA; (I) Methyl carbocyclic (4'-CH2-CH(CH3)-2') BNA; (J) propylene carbocyclic (4'-(CH2)3-2') BNA, and (K) Vinyl BNA.

[0280] [ka] In the formula, Bx is a base moiety, and R is independently a protecting group, C1-C6 alkyl, or C1-C6 alkoxy.

[0281] In certain embodiments (LNA), the nucleoside having a bicyclic sugar has the following general formula: [ka] [In the formula, B is a nucleobase; X and Y are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a covalent bond to a phosphorus moiety or a support, etc. (see WO98 / 39352). A typical specific example is a nucleoside represented by the following formula: [ka] Examples of nucleotides include those represented by the following formula:

[0282] In certain embodiments (GuNA), the bicyclic nucleoside has the general formula: [ka] [In the formula, B is a nucleic acid base, and R3, R4, R5, and R6 are each independently a hydrogen atom or a C 1-6 R7 and R8 are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a covalent bond to a phosphorus moiety or a support, and R9 and R 10 , R 11 Each independently represents a hydrogen atom or C which may be substituted with one or more substituents. 1-6 It is a protecting group for an alkyl group or an amino group. (See, for example, International Publication No. WO 2014 / 046212 and International Publication No. WO 2017 / 047816).

[0283] In certain embodiments (ALNA[mU]), the nucleoside containing a bicyclic sugar has the following general formula (I): [ka] [In the formula, B is a nucleobase; R1, R2, R3 and R4 each independently represent a hydrogen atom or a C 1-6 is an alkyl group; R5 and R6 are each independently a hydrogen atom, a protecting group for a hydroxyl group, an optionally substituted phosphate group, a phosphorus moiety or a covalent bond to a support, or the like; m is 1 or 2; X is represented by the following formula (II-1): [ka] is a group represented by the formula: The symbols shown in formula (II-1): [ka] indicates the point of attachment to the 2'-amino group; One of R7 and R8 is a hydrogen atom, and the other is a methyl group which may be substituted with one or more substituents. (For example, see Japanese Patent Application No. 2018-212424.) A typical example is a nucleoside in which one of R7 and R8 is a hydrogen atom and the other is an unsubstituted methyl group.

[0284] In certain embodiments (ALNA[ipU]), the nucleoside containing a bicyclic sugar is a nucleoside having the general formula (I) as defined above in ALNA[mU], wherein: X is represented by the following formula (II-1): [ka] is a group represented by the formula: One of R7 and R8 is a hydrogen atom, and the other is an isopropyl group which may be substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example is a nucleoside in which one of R7 and R8 is a hydrogen atom, and the other is an unsubstituted isopropyl group.

[0285] In certain embodiments (ALNA[Trz]), the bicyclic nucleoside is a nucleoside having the general formula (I) above, wherein X is a nucleoside having the following formula (II-2): [ka] is a group represented by the formula: A is a triazolyl group which may be substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example of ALNA[Trz] is a nucleoside in which A is a triazolyl group which may have one or more methyl groups, more specifically, a 1,5-dimethyl-1,2,4-triazol-3-yl group.

[0286] In certain embodiments (ALNA[Oxz]), there is provided a nucleoside having the general formula (I) as defined above in ALNA[mU], wherein: X is represented by the following formula (II-2): [ka] is a group represented by the formula: A is an oxadiazolyl group optionally substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example is a nucleoside or nucleotide in which A is an oxadiazolyl group optionally having one or more methyl groups, more specifically, a 5-methyl-1,2,4-oxadiazol-3-yl group.

[0287] In certain embodiments (ALNA[Ms]), the bicyclic nucleoside is a nucleoside having the general formula (I) above, wherein X is a nucleoside having the following general formula (II-3): [ka] is a group represented by the formula: M is a sulfonyl group substituted with a methyl group which may be substituted with one or more substituents (see, for example, Japanese Patent Application No. 2018-212424). A typical example of ALNA[Ms] is a nucleoside in which M is a sulfonyl group substituted with an unsubstituted methyl group.

[0288] In certain embodiments, nucleosides are modified by replacement of the ribosyl ring with a sugar surrogate, including, but not limited to, replacement of the ribosyl ring with a surrogate ring system (sometimes referred to as a DNA analogue), such as a morpholino ring, a cyclohexenyl ring, a cyclohexyl ring, or a tetrahydropyranyl ring, such as having one of the following formulas: [ka]

[0289] In certain embodiments, a sugar substitute is selected having the following formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T3 and T4 are each independently an internucleoside linking group that links a tetrahydropyran nucleoside analog to an oligomeric compound, or one of T3 and T4 is an internucleoside linking group that links a tetrahydropyran nucleoside analog to an oligomeric compound or oligonucleotide, and the other of T3 and T4 is H, a hydroxyl protecting group, a linking conjugate group, or a 5'- or 3'-terminal group; q1, q2, q3, q4, q5, q6 and q7 are each independently H, C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, C2-C6 alkynyl or substituted C2-C6 alkynyl; One of R1 and R2 is hydrogen, and the other is selected from halogen, substituted or unsubstituted alkoxy, NJ1J2, SJ1, N3, OC(=X)J1, OC(=X)NJ1J2, NJ3C(=X)NJ1J2, and CN (wherein X is O, S, or NJ1, and each J1, J2, and J3 is independently H or C1-C6 alkyl).

[0290] In certain embodiments, q1, q2, q3, q4, q5, q6, and q7 are each H. In certain embodiments, at least one of q1, q2, q3, q4, q5, q6, and q7 is other than H. In certain embodiments, at least one of q1, q2, q3, q4, q5, q6, and q7 is methyl. In certain embodiments, THP nucleosides are provided in which one of R1 and R2 is F. In certain embodiments, R1 is fluoro and R2 is H; R1 is methoxy and R2 is H, and R1 is methoxyethoxy and R2 is H.

[0291] Such sugar substitutes include, but are not limited to, those referred to in the art as hexitol nucleic acid (HNA), altritol nucleic acid (ANA), and mannitol nucleic acid (MNA) (Leumann, CJ, Bioorg. & Med. Chem. 2003, 143:1311-1323). .,2002,10,841-854).

[0292] In certain embodiments, the sugar surrogate contains a ring having more than five atoms and more than one heteroatom. For example, its use in nucleosides and oligomeric compounds containing morpholino sugar moieties has been reported (see, e.g., Braaschet et al., Biochemistry, 2002, 41, 4503-4510; and U.S. Patents 5,698,685; 5,166,315; 5,185,444; and 5,034,506).

[0293] As used herein, the term "morpholino" refers to a sugar surrogate having the following structure: [ka]

[0294] In certain embodiments, morpholinos can be modified, for example, by adding or altering various substituents from the morpholino structures shown above. Such sugar surrogates are referred to herein as "modified morpholinos."

[0295] In certain embodiments, the oligonucleotides comprise one or more modified cyclohexenyl nucleosides, which are nucleosides having a six-membered cyclohexenyl in place of the pentofuranosyl residue of naturally occurring nucleosides.Modified cyclohexenyl nucleosides include, but are not limited to, those described in the art (e.g., co-owned WO 2010 / 036696 published April 10, 2010; Robeynset al., J. Am. Chem. Soc., 2008, 130(6), 1979-1984; Horvathet al., Tetrahedron Letters, 2007, 48, 3621-3623; Nauwelaerts et al., J. Am. Chem. Soc., 2007, 129(30), 9340-9348; Guet al., Nucleosides, Nucleotides & Nucleic Acids, 2005, 24(5-7), 993-998; Nauwelaerts et al., Nucleic Acids, 2005, 24(5-7), 993-998; AcidsResearch,2005,33(8),2452-2463;Robeyns et al.,Acta Crystallographica,Section F:StructuralBiology and Crystallization Communications,2005,F61(6),585-586;Guet al.,Tetrahedron,2004,60(9),2111-2123;Guet al.,Oligonucleotides,2003,13(6),479-489;Wanget al.,J.Org.Chem.,2003,68,4499-4505;Verbeureet al.,NucleicAcids Research,2001,29(24),4941-4947;Wangetal.,J.Org.Chem.,2001,66,8478-82;Wang et al. al., Nucleosides, Nucleotides & Nucleic Acids, 2001, 20(4-7), 785-788; Wang et al., J. Am. Chem., 2000, 122, 8595-8602; WO06 / 047842; and WO01 / 049687; the texts of each of which are incorporated herein by reference in their entireties.

[0296] Certain modified cyclohexenyl nucleosides have the formula: [ka] During the ceremony, Bx is a heterocyclic base moiety; T3 and T4 are each independently an internucleoside linking group that links a cyclohexenyl nucleoside analog to an oligonucleotide compound, or one of T3 and T4 is an internucleoside linking group that links a tetrahydropyran nucleoside analog to an oligonucleotide compound and the other of T3 and T4 is H, a hydroxyl protecting group, a linking conjugate group, or a 5'- or 3'-terminal group; q1, q2, q3, q4, q5, q6, q7, q8, and q9 are each independently H, C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, C2-C6 alkynyl, substituted C2-C6 alkynyl, or other sugar substituents.

[0297] Many other bicyclic and tricyclic sugar surrogate ring systems are known in the art that can be used to modify nucleosides for incorporation into oligonucleotides (see, for example, review: Leumann, Christian J., Bioorg. & Med. Chem., 2002, 10, 841-854). Such ring systems can undergo various further substitutions to enhance activity.

[0298] Methods for the preparation of modified sugars are well known to those of skill in the art. Some representative US patents that teach the preparation of such modified sugars include, but are not limited to, US: 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; Nos. 5,591,722; 5,597,909; 5,610,300; 5,627,053; 5,639,873; 5,646,265; 5,670,633; 5,700,920; 5,792,847 and 6,600,032, and WO 2005 / 121371, each of which is incorporated by reference in its entirety.

[0299] In nucleotides having modified sugar moieties, the nucleobase moieties (natural, modified or a combination thereof) are maintained upon hybridization with an appropriate nucleic acid target.

[0300] Modified Nucleobases Nucleobase (or base) modifications or substitutions are structurally distinguishable from naturally occurring or synthetic unmodified nucleobases, and are functionally compatible with such unmodified nucleobases. Both natural and modified nucleobases can participate in hydrogen bonding. Such nucleobase modifications can impart nuclease stability, binding affinity, or some other beneficial biological property to the modified oligonucleotide. Modified nucleobases include synthetic and natural nucleobases, such as 5-methylcytosine (5-me-C). Certain nucleobase substitutions, including 5-methylcytosine substitutions, are particularly useful for increasing the binding affinity of modified oligonucleotides to target nucleic acids. For example, 5-methylcytosine substitutions have been shown to increase nucleic acid duplex stability by 0.6-1.2°C (Sanghvi, YS, Crooke, ST and Lebleu, B., eds., Antisense Research and Applications, CRC Press, Boca Raton, 1993, pp. 276-278).

[0301] Further modified nucleobases include 5-hydroxymethylcytosine, 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 (-C≡C-CH3) uracil and cytosine and other alkynyl derivatives of pyrimidine bases, 6-azouracil, cytosine and thymine, 5-uracil, cytosine and thymine, cytosine ... Examples of suitable uracils include pseudouracil, 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl and other 8-substituted adenines and guanines, 5-halo, especially 5-bromo, 5-trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 2-F-adenine, 2-amino-adenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-deazaadenine, 3-deazaguanine and 3-deazaadenine.

[0302] Heterocyclic base moieties can also include those in which the purine or pyrimidine base is replaced with other heterocycles, such as 7-deaza-adenine, 7-deazaguanosine, 2-aminopyridine, and 2-pyridone.Nucleobases that are particularly useful for increasing the binding affinity of modified oligonucleotides include 5-substituted pyrimidines, 6-azapyrimidines, and N-2, N-6, and O-6 substituted purines, including 2-aminopropyladenine, 5-propynyluracil, and 5-propynylcytosine.

[0303] In certain embodiments, the modified oligonucleotide targeted to DUX4 nucleic acid comprises one or more modified nucleobases.In certain embodiments, the modified oligonucleotide targeted to DUX4 nucleic acid comprises one or more modified nucleobases.In certain embodiments, the modified nucleobase is 5-methylcytosine.In certain embodiments, each cytosine is 5-methylcytosine.

[0304] Certain modified oligonucleotide motifs In certain embodiments, modified oligonucleotides targeted to DUX4 nucleic acids have chemically modified subunits arranged in a pattern or motif to confer properties on the modified oligonucleotide, such as enhanced inhibitory activity, increased binding affinity for the target nucleic acid, or resistance to degradation by in vivo nucleases.

[0305] Chimeric modified oligonucleotides typically contain at least one modified region to confer increased resistance to degradation by nucleases, increased cellular uptake, increased binding affinity for the target nucleic acid, and / or increased inhibitory activity. A second region of the chimeric modified oligonucleotide can optionally serve as a substrate for the intracellular endonuclease RNase H, which cleaves the RNA strand of an RNA:DNA duplex.

[0306] Modified oligonucleotides having a gapmer motif are chimeric modified oligonucleotides. In a gapmer, an internal region having a number of nucleotides that support RNase H cleavage is located between an external region having a number of nucleotides that are chemically different from the nucleosides of the internal region. In the case of modified oligonucleotides having a gapmer motif, the gap segment generally serves as a substrate for cleavage by an endonuclease, while the wing segments contain modified nucleosides. In certain embodiments, the gapmer regions are distinguished by the type of sugar moiety that each distinct region comprises. In some embodiments, the types of sugar moieties used to distinguish the gapmer region can include β-D-ribonucleosides, β-D-deoxyribonucleosides, 2'-modified nucleosides (such 2'-modified nucleosides can include 2'-MOE and 2'-O-CH3, among others), and bicyclic sugar modified nucleosides (such bicyclic sugar modified nucleosides can include those having LNA, GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Trz], and / or ALNA[Oxz]). The wing-gap-wing motif is often described as "XYZ," where "X" represents the length of the 5' wing region, "Y" represents the length of the gap region, and "Z" represents the length of the 3' wing region. As used herein, a gapmer described as "XYZ" has a configuration in which the gap segment is located immediately adjacent to each of the 5' wing segment and the 3' wing segment. Thus, there are no intervening nucleotides between the 5' wing segment and the gap segment or between the gap segment and the 3' wing segment. Any of the modified oligonucleotides described herein can have a gapmer motif. In some embodiments, X and Z are the same, while in other embodiments they are different. In preferred embodiments, Y is 8 to 16 nucleotides. X, Y, or Z can be any of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30 or more nucleotides.Thus, gapmers include, but are not limited to, for example, 2-10-3, 2-14-2, 2-15-2, 2-16-2, 3-6-7, 3-7-5, 3-8-3, 3-8-4, 3-8-5, 3-9-2, 3-9-3, 3-9-4, 3-9-5, 3-9-8, 3-10-2, 3-10-3, 3-10-4, 3-11-3, 3-12-3, 3-14-3, 4-7-4, 4-7-5, 4-8-3, 4-8-4, 4-9-3, 4-10-3, 5-6-4, 5-6-5, 5-7-3, 5-7-4, 5-8-3, 5-8-4, or 7-6-3.

[0307] In certain embodiments, modified oligonucleotides targeted to DUX4 nucleic acids have a 3-10-3 gapmer motif. In certain embodiments, modified oligonucleotides targeted to DUX4 nucleic acids have a 3-9-3 gapmer motif. In certain embodiments, modified oligonucleotides targeted to DUX4 nucleic acids have a 3-9-4 gapmer motif. In certain embodiments, modified oligonucleotides targeted to DUX4 nucleic acids have a 3-8-5 gapmer motif.

[0308] In certain embodiments, these gapmer modified oligonucleotides comprise at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18, at least 19, at least 20, at least 21, at least 22, at least 23, at least 24, at least 25, at least 26, at least 27, at least 28, at least 29, or at least 30 consecutive nucleobases of the nucleobase sequence set forth in any one of SEQ ID NOs: 2, 3, 4, 7-64, 69-97, or 102-112 of the Sequence Listing) of any of the exemplary modified oligonucleotides described herein.

[0309] In certain embodiments, the present invention provides oligomeric compounds comprising oligonucleotides. In certain embodiments, such oligonucleotides comprise one or more chemical modifications. In certain embodiments, chemically modified oligonucleotides comprise one or more modified sugars. In certain embodiments, chemically modified oligonucleotides comprise one or more modified nucleobases. In certain embodiments, chemically modified oligonucleotides comprise one or more modified internucleoside linkages. In certain embodiments, the chemical modifications (sugar modifications, nucleobase modifications and / or linkage modifications) define a pattern or motif. In certain embodiments, the patterns of chemical modifications of sugar moieties, internucleoside linkages and nucleobases are each independent of each other. Thus, an oligonucleotide can be described by its sugar modification motif, internucleoside linkage motif and / or nucleobase modification motif (as used herein, nucleobase modification motif describes chemical modifications to nucleobases independent of the sequence of nucleobases).

[0310] Certain glycomotifs In certain embodiments, oligonucleotides contain one or more types of modified sugar moieties and / or naturally occurring sugar moieties arranged along the oligonucleotide or regions thereof in defined patterns or sugar modification motifs, which can include any of the sugar modifications discussed herein and / or other known sugar modifications.

[0311] In certain embodiments, an oligonucleotide comprises or consists of a region having a gapmer sugar modification motif, which comprises two exterior regions, or "wing segments," and one interior region, or "gap segment." The three regions of a gapmer motif (the 5' wing segment, the gap segment, and the 3' wing segment) form a contiguous sequence of nucleosides in which at least some of the sugar moieties of the nucleosides of each wing segment differ from at least some of the sugar moieties of the nucleosides of the gap segment. In particular, at least the sugar moiety of the nucleoside of each wing segment closest to the gap segment (the 3'-most nucleoside of the 5' wing segment and the 5'-most nucleoside of the 3' wing segment) differs from the sugar moiety of the nucleoside of the adjacent gap segment, thus defining a boundary site between the wing segment and the gap segment. In certain embodiments, the sugar moieties within the gap segment are the same as each other. In certain embodiments, the gap segment comprises one or more nucleosides having a sugar moiety that is different from the sugar moiety of one or more other nucleosides in the gap segment. In certain embodiments, the sugar modification motifs of the two wing segments are identical to each other (symmetric gapmer). In certain embodiments, the sugar modification motif of the 5' wing segment is different from the sugar modification motif of the 3' wing segment (asymmetric gapmer).

[0312] Certain 5' wing segments In certain embodiments, the 5' wing segment of a gapmer consists of one to five linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of two to five linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of three to five linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of four or five linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of one to four linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of one to three linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of one or two linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of two to four linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of two or three linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of three or four linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of one nucleoside. In certain embodiments, the 5' wing segment of a gapmer consists of two linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of three linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of four linked nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of five linked nucleosides.

[0313] In certain embodiments, the 5' wing segment of the gapmer comprises at least one bicyclic nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least two bicyclic nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises at least three bicyclic nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises at least four bicyclic nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises at least one constrained ethyl nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one LNA-containing nucleoside, GuNA-containing nucleoside, ALNA[Ms]-containing nucleoside, ALNA[mU]-containing nucleoside, ALNA[ipU]-containing nucleoside, ALNA[Trz]-containing nucleoside and / or ALNA[Oxz]-containing nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of a gapmer is a bicyclic nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of a gapmer is a constrained ethyl nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of a gapmer is an LNA-containing nucleoside, a GuNA-containing nucleoside, an ALNA[Ms]-containing nucleoside, an ALNA[mU]-containing nucleoside, an ALNA[ipU]-containing nucleoside, an ALNA[Trz]-containing nucleoside and / or an ALNA[Oxz]-containing nucleoside.

[0314] In certain embodiments, the 5' wing segment of the gapmer comprises at least one non-bicyclic modified nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one 2'-substituted nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one, e.g., three, four, or five, 2'-MOE nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises at least one 2'-OMe nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of the gapmer is a non-bicyclic modified nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of the gapmer is a 2'-substituted nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of the gapmer is a 2'-MOE nucleoside. In certain embodiments, each nucleoside in the 5' wing segment of a gapmer is a 2'-OMe nucleoside.

[0315] In certain embodiments, the 5' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one non-bicyclic modified nucleoside. In certain embodiments, the 5' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-substituted nucleoside. In certain embodiments, the 5' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-MOE nucleoside. In certain embodiments, the 5' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-OMe nucleoside. In certain embodiments, the 5' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-deoxynucleoside.

[0316] In certain embodiments, the 5' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one non-bicyclic modified nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-substituted nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-MOE nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-OMe nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-deoxynucleoside.

[0317] In certain embodiments, the 5' wing segment of a gapmer comprises at least one modified nucleoside selected from a 2'-MOE nucleoside, a 2'-OMe nucleoside, an LNA-containing nucleoside, a GuNA-containing nucleoside, an ALNA[Ms]-containing nucleoside, an ALNA[mU-containing nucleoside], an ALNA[ipU]-containing nucleoside, an ALNA[Trz]-containing nucleoside and / or an ALNA[Oxz]-containing nucleoside. In certain embodiments, the 5' wing segment of a gapmer comprises at least two modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 5' wing segment of a gapmer comprises at least three modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 5' wing segment of a gapmer comprises at least four modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides.In certain embodiments, the 5' wing segment of a gapmer comprises at least five modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU-containing nucleosides], ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides.

[0318] In certain embodiments, the 5' wing segment of the gapmer comprises two LNA-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises three LNA-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises four LNA-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two GuNA-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises three GuNA-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises three ALNA[mU]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises three ALNA[ipU]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two LNA-containing nucleosides and one GuNA-containing nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises three ALNA[Trz]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides and one 2'-OMe nucleoside. In certain embodiments, the 5' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides and two 2'-OMe nucleosides.

[0319] In certain embodiments, the 5' wing segment of the gapmer comprises three constrained ethyl nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two bicyclic nucleosides and two non-bicyclic modified nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two constrained ethyl nucleosides and two 2'-OMe nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two bicyclic nucleosides and two non-bicyclic modified nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two constrained ethyl nucleosides and two 2'-OMe nucleosides. In certain embodiments, the 5' wing segment of the gapmer comprises two constrained ethyl nucleosides and three 2'-OMe nucleosides.

[0320] In certain embodiments, the 5' wing segment of the gapmer consists of one ALNA[Ms]-containing nucleoside. In certain embodiments, the 5' wing segment of the gapmer consists of two linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of three linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of four linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of five linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of linked 1, 2 or 3 ALNA[Ms]-containing nucleosides and one 2'-OMe nucleoside. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms] containing nucleosides and two 2'-OMe nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms] containing nucleosides and three 2'-OMe nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of three ALNA[Ms] containing nucleosides and one 2'-MOE nucleoside linked together. In certain embodiments, the 5' wing segment of the gapmer consists of two ALNA[Ms] containing nucleosides and two 2'-MOE nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of three LNA containing nucleosides and two 2'-MOE nucleosides linked together. In certain embodiments, the 5' wing segment of a gapmer consists of two LNA-containing nucleosides and two 2'-MOE nucleosides linked together. In certain embodiments, the 5' wing segment of a gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises one 5-methylcytosine. In certain embodiments, the 5' wing segment of a gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises two 5-methylcytosines. In certain embodiments, the 5' wing segment of a gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises three 5-methylcytosines.

[0321] Certain 3' wing segments In certain embodiments, the 3' wing segment of a gapmer consists of one to eight linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of two to five linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of three to five linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of four or five linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of one to four linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of one to three linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of one or two linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of two to four linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of two or three linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of three or four linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of one nucleoside. In certain embodiments, the 3' wing segment of a gapmer consists of two linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of three linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of four linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of five linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of six linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of seven linked nucleosides. In certain embodiments, the 3' wing segment of a gapmer consists of eight linked nucleosides.

[0322] In certain embodiments, the 3' wing segment of the gapmer comprises at least one bicyclic nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least two bicyclic nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises at least three bicyclic nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises at least four bicyclic nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises at least one constrained ethyl nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one LNA-containing nucleoside, GuNA-containing nucleoside, ALNA[Ms]-containing nucleoside, ALNA[mU]-containing nucleoside, ALNA[ipU]-containing nucleoside, ALNA[Trz]-containing nucleoside and / or ALNA[Oxz]-containing nucleoside. In certain embodiments, each nucleoside in the 3' wing segment of a gapmer is a bicyclic nucleoside. In certain embodiments, each nucleoside in the 3' wing segment of a gapmer is a constrained ethyl nucleoside. In certain embodiments, each nucleoside in the 3' wing segment of a gapmer is an LNA-containing nucleoside, a GuNA-containing nucleoside, an ALNA[Ms]-containing nucleoside, an ALNA[mU]-containing nucleoside, an ALNA[ipU]-containing nucleoside, an ALNA[Trz]-containing nucleoside and / or an ALNA[Oxz]-containing nucleoside.

[0323] In certain embodiments, the 3' wing segment of the gapmer comprises at least one non-bicyclic modified nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one 2'-substituted nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one 2'-MOE nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one 2'-OMe nucleoside. In certain embodiments, each nucleoside of the 3' wing segment of the gapmer is a non-bicyclic modified nucleoside. In certain embodiments, each nucleoside of the 3' wing segment of the gapmer is a 2'-substituted nucleoside. In certain embodiments, each nucleoside of the 3' wing segment of the gapmer is a 2'-MOE nucleoside. In certain embodiments, each nucleoside in the 3' wing segment of a gapmer is a 2'-OMe nucleoside.

[0324] In certain embodiments, the 3' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one non-bicyclic modified nucleoside. In certain embodiments, the 3' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-substituted nucleoside. In certain embodiments, the 3' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-MOE nucleoside. In certain embodiments, the 3' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-OMe nucleoside. In certain embodiments, the 3' wing segment of a gapmer comprises at least one bicyclic nucleoside and at least one 2'-deoxynucleoside.

[0325] In certain embodiments, the 3' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one non-bicyclic modified nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-substituted nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-MOE nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-OMe nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises at least one constrained ethyl nucleoside and at least one 2'-deoxynucleoside.

[0326] In certain embodiments, the 3' wing segment of a gapmer comprises at least one modified nucleoside selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises at least two modified nucleosides selected from a 2'-MOE nucleoside, a 2'-OMe nucleoside, an LNA-containing nucleoside, a GuNA-containing nucleoside, an ALNA[Ms]-containing nucleoside, an ALNA[mU]-containing nucleoside, an ALNA[ipU]-containing nucleoside, an ALNA[Trz]-containing nucleoside and / or an ALNA[Oxz]-containing nucleoside. In certain embodiments, the 3' wing segment of a gapmer comprises at least three modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises at least four modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides.In certain embodiments, the 3' wing segment of a gapmer comprises at least five modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises at least six modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises at least seven modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises at least eight modified nucleosides selected from 2'-MOE nucleosides, 2'-OMe nucleosides, LNA-containing nucleosides, GuNA-containing nucleosides, ALNA[Ms]-containing nucleosides, ALNA[mU]-containing nucleosides, ALNA[ipU]-containing nucleosides, ALNA[Trz]-containing nucleosides and / or ALNA[Oxz]-containing nucleosides.

[0327] In certain embodiments, the 3' wing segment of the gapmer comprises two LNA-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three LNA-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises four LNA-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises two GuNA-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three GuNA-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[mU]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[ipU]-containing nucleosides. In certain embodiments, the 3' wing of the gapmer comprises two LNA-containing nucleosides and one GuNA-containing nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[Trz]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides and one 2'-OMe nucleoside. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides and two 2'-OMe-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises four 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises five 2'-MOE. In certain embodiments, the 3' wing segment of a gapmer comprises three ALNA[Ms]-containing nucleosides and one 2'-MOE-containing nucleoside. In certain embodiments, the 3' wing segment of a gapmer comprises three ALNA[Ms]-containing nucleosides and two 2'-MOE nucleosides.In certain embodiments, the 3' wing segment of the gapmer comprises two ALNA[Ms]-containing nucleosides and two 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises two ALNA[Ms]-containing nucleosides and three 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises three ALNA[Ms]-containing nucleosides and five 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises one ALNA[Ms]-containing nucleoside and three 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer comprises two LNA-containing nucleosides and two 2'-MOE nucleosides.

[0328] In certain embodiments, the 3' wing segment of a gapmer comprises three constrained ethyl nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises two bicyclic nucleosides and two non-bicyclic modified nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises two constrained ethyl nucleosides and two 2'-OMe nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises two bicyclic nucleosides and two non-bicyclic modified nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises two constrained ethyl nucleosides and two 2'-OMe nucleosides. In certain embodiments, the 3' wing segment of a gapmer comprises two constrained ethyl nucleosides and three 2'-OMe nucleosides.

[0329] In certain embodiments, the 3' wing segment of the gapmer consists of one ALNA[Ms]-containing nucleoside. In certain embodiments, the 3' wing segment of the gapmer consists of two linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer consists of three linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer consists of four linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer consists of five linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 3' wing segment of the gapmer consists of three, four or five linked 2'-MOE nucleosides. In certain embodiments, the 3' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and one 2'-OMe nucleoside. In certain embodiments, the 3' wing segment of a gapmer consists of one, two or three ALNA[Ms] containing nucleosides and two 2'-OMe nucleosides linked together. In certain embodiments, the 3' wing segment of a gapmer consists of one, two or three ALNA[Ms] containing nucleosides and three 2'-OMe nucleosides linked together. In certain embodiments, the 3' wing segment of a gapmer consists of one, two or three ALNA[Ms] containing nucleosides and one 2'-MOE nucleoside linked together. In certain embodiments, the 3' wing segment of a gapmer consists of one, two or three ALNA[Ms] containing nucleosides and two 2'-MOE nucleosides linked together. In certain embodiments, the 3' wing segment of a gapmer consists of one, two or three ALNA[Ms]-containing nucleosides and three 2'-MOE nucleosides linked together. In certain embodiments, the 3' wing segment of a gapmer consists of one, two or three ALNA[Ms]-containing nucleosides and five 2'-MOE nucleosides linked together. In certain embodiments, the 3' wing segment of a gapmer consists of two LNA-containing nucleosides and two 2'-MOE nucleosides linked together. In certain embodiments, the 3' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and includes one 5-methylcytosine. In certain embodiments, the 3' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and includes two 5-methylcytosines. In certain embodiments, the 3' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and includes three 5-methylcytosines. In certain embodiments, the 3' wing segment of the gapmer consists of one, two, three, four or five linked 2'-MOE nucleosides and includes one 5-methylcytosine.

[0330] In certain embodiments, the 5' wing segment of the gapmer consists of one ALNA[Ms]-containing nucleoside and the 3' wing segment consists of one ALNA[Ms]-containing nucleoside. In certain embodiments, the 5' wing segment of the gapmer consists of two linked ALNA[Ms]-containing nucleosides and the 3' wing segment consists of two linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of three linked ALNA[Ms]-containing nucleosides and the 3' wing segment consists of three linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of four linked ALNA[Ms]-containing nucleosides and the 3' wing segment consists of four linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of a gapmer consists of five linked ALNA[Ms]-containing nucleosides and the 3' wing segment consists of five linked ALNA[Ms]-containing nucleosides. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms]-containing nucleosides and one 2'-OMe nucleoside linked together, and the 3' wing segment consists of one, two or three ALNA[Ms]-containing nucleosides and one 2'-OMe nucleoside linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms]-containing nucleosides and two 2'-OMe nucleosides linked together, and the 3' wing segment consists of one, two or three ALNA[Ms]-containing nucleosides and two 2'-OMe nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms]-containing nucleosides and three 2'-OMe nucleosides linked together, and the 3' wing segment consists of one, two or three ALNA[Ms]-containing nucleosides and three 2'-OMe nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms]-containing nucleosides and one or two 2'-MOE nucleosides linked together, and the 3' wing segment consists of one, two or three ALNA[Ms]-containing nucleosides and one or two 2'MOE nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three ALNA[Ms]-containing nucleosides linked together, and the 3' wing segment consists of one, two or three ALNA[Ms]-containing nucleosides and one, two or three 2'-MOE nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two, or three ALNA[Ms]-containing nucleosides linked together and the 3' wing segment consists of one, two, three, four, or five 2'-MOE nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer consists of one, two, three, four, or five 2'-MOE nucleosides linked together and the 3' wing segment consists of one, two, or three ALNA[Ms]-containing nucleosides linked together. In certain embodiments, the 5' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises one 5-methylcytosine, and the 3' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises one 5-methylcytosine. In certain embodiments, the 5' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises two 5-methylcytosines, and the 3' wing of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises one 5-methylcytosine. In certain embodiments, the 5' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises two 5-methylcytosines, and the 3' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises two 5-methylcytosines. In certain embodiments, the 5' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises three 5-methylcytosines, and the 3' wing segment of the gapmer is comprised of one, two or three linked ALNA[Ms]-containing nucleosides and comprises three 5-methylcytosines. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and comprises a 5-methylcytosine, and the 3' wing segment of the gapmer consists of one, two, three, four or five linked 2'-MOE nucleosides and comprises a 5-methylcytosine. In certain embodiments, the 5' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and the 3' wing segment of the gapmer consists of one, two or three linked ALNA[Ms]-containing nucleosides and one, two or three 2'-MOE nucleosides and comprises a 5-methylcytosine.

[0331] In certain embodiments, the gap segment of a gapmer comprises 10 contiguous nucleosides, with at any of the 1st, 2nd, 3rd, 4th, 5th, 6th, 7th, 8th, 9th or 10th nucleosides being a 2'-OMe nucleoside, and the remaining nucleosides being deoxynucleosides.

[0332] Compositions and methods for formulating pharmaceutical compositions For the preparation of pharmaceutical compositions or formulations, modified oligonucleotides can be mixed with one or more pharma- ceutically acceptable active or inactive substances.The composition and method for the formulation of pharmaceutical compositions depend on several criteria, including but not limited to, the route of administration, the extent of disease, or the dose to be administered.

[0333] Modified oligonucleotides targeting DUX4 nucleic acid can be used in pharmaceutical compositions by combining modified oligonucleotides with suitable pharma- ceutical acceptable diluents or carriers. Pharmaceutically acceptable diluents include phosphate buffered saline (PBS). PBS is a suitable diluent for use in parenterally delivered compositions. Thus, in one embodiment, pharmaceutical compositions comprising modified oligonucleotides targeting DUX4 nucleic acid and pharma-ceutical acceptable diluents are used in the methods described herein. In certain embodiments, the pharma-ceutical acceptable diluent is PBS.

[0334] Pharmaceutical compositions comprising modified oligonucleotides include any pharma- ceutical acceptable salts, esters or salts of such esters or any other oligonucleotides that can provide (directly or indirectly) biologically active metabolites or residues thereof when administered to animals, including humans. Thus, for example, the present disclosure also relates to pharma-ceutical acceptable salts, prodrugs, pharma-ceutical acceptable salts of such prodrugs, and other bioequivalents of modified oligonucleotides. Suitable pharma-ceutical acceptable salts include, but are not limited to, sodium salts and potassium salts.

[0335] Prodrugs can involve the incorporation of additional nucleosides at one or both ends of a modified oligonucleotide that are cleaved by endogenous nucleases in the body to form the active modified oligonucleotide.

[0336] Conjugate Modified Oligonucleotides Modified oligonucleotides can be covalently linked to one or more moieties or conjugates that enhance the activity, cellular distribution or cellular uptake of the resulting modified oligonucleotide.Typical conjugation groups include cholesterol moieties and lipid moieties.Additional conjugation groups include carbohydrates, phospholipids, biotin, phenazine, folic acid, phenanthridine, anthraquinone, acridine, fluorescein, rhodamine, coumarin and dyes.

[0337] Modified oligonucleotides can also be modified to have one or more stabilizing groups, which are generally attached to one or both ends of the modified oligonucleotide, to enhance properties such as, for example, nuclease stability. Cap structures are included in the stabilizing groups. These end modifications can protect modified oligonucleotides with terminal nucleic acids from exonuclease degradation and aid in intracellular delivery and / or localization. The caps can be present at the 5' end (5' cap) or 3' end (3' cap), or can be present at both ends. Cap structures are well known in the art and include, for example, inverted deoxy abasic caps. Additional 3' and 5' stabilizing groups that can be used to cap one or both ends of modified oligonucleotides to provide nuclease stability include those disclosed in WO03 / 004602.

[0338] Cell culture and modified oligonucleotide treatment The effect of modified oligonucleotides on the level, activity or expression of DUX4 nucleic acid can be tested in vitro in various cell types. The cell types used for such analysis are available from commercial suppliers (e.g., American Type Culture Collection, Manassus, VA; Zen-Bio, Inc., Research Triangle Park, NC; Clonetics Corporation, Walkersville, MD), and the cells are cultured according to the supplier's instructions using commercially available reagents (e.g., Invitrogen Life Technologies, Carlsbad, CA). Exemplary cell types include, but are not limited to, C2C12 cells, HepG2 cells, Hep3B cells, primary hepatocytes, A549 cells, GM04281 fibroblasts, and LLC-MK2 cells. These cells can be used by transfecting with a vector expressing human DUX4 mRNA. The vector is preferably expressed as a fusion protein with a reporter gene such as luciferase or GFP, for example, psiCHECK-2 vector (Promega).

[0339] In vitro testing of modified oligonucleotides Methods for treating cells with modified oligonucleotides are described herein, which can be appropriately modified depending on the type of modified oligonucleotide.

[0340] Generally, cells are treated with modified oligonucleotides when they reach approximately 60-80% confluence in culture.

[0341] The modified oligonucleotides are introduced into cells, for example, by lipofection. One commonly used reagent for introducing modified oligonucleotides into cultured cells is the cationic lipid transfection reagent LIPOFECTIN® (Invitrogen, Carlsbad, Calif.). The modified oligonucleotides are mixed with LIPOFECTIN® in OPTI-MEM® 1 (Invitrogen, Carlsbad, Calif.) to obtain the desired final concentration of modified oligonucleotide and a LIPOFECTIN® concentration that typically ranges from 2-12 μg / mL per 100 nM modified oligonucleotide.

[0342] Another reagent used to introduce modified oligonucleotides into cultured cells includes LIPOFECTAMINE2000® (Invitrogen, Carlsbad, Calif.). The modified oligonucleotides are mixed with LIPOFECTAMINE2000® in OPTI-MEM® 1 serum-reduced medium (Invitrogen, Carlsbad, Calif.) to obtain the desired concentration of modified oligonucleotide and a LIPOFECTAMINE® concentration that typically ranges from 2-12 μg / mL per 100 nM modified oligonucleotide.

[0343] Another reagent used to introduce modified oligonucleotides into cultured cells includes Cytofectin® (Invitrogen, Carlsbad, Calif.). The modified oligonucleotides are mixed with Cytofectin® in OPTI-MEM® 1 serum-reduced medium (Invitrogen, Carlsbad, Calif.) to obtain the desired concentration of modified oligonucleotide and a Cytofectin® concentration that typically ranges from 2-12 μg / mL per 100 nM modified oligonucleotide.

[0344] Another technique used to introduce modified oligonucleotides into cultured cells includes electroporation.

[0345] Modified oligonucleotides can be introduced into cells without using Lipofectin, etc. In this case, the method of suppressing the expression of the target gene by modified oligonucleotides is called the Gymnosis method.

[0346] Cells are treated with modified oligonucleotides by conventional methods. Typically, cells are harvested 16-48 hours after modified oligonucleotide treatment, at which time RNA or protein levels of the target nucleic acid are measured by methods known in the art and described herein. Generally, when treatments are performed in multiple replicates, data are presented as an average of the replicate treatments.

[0347] The concentration of modified oligonucleotides used varies depending on the cell line. Methods for determining the optimal modified oligonucleotide concentration for a particular cell line are well known in the art. When transfecting with LIPOFECTAMINE2000®, LIPOFECTIN or Cytofectin, modified oligonucleotides are typically used at concentrations ranging from 1 nM to 300 nM. When transfecting with electroporation, modified oligonucleotides are used at higher concentrations ranging from 625 to 20,000 nM. From the inhibition rate of gene expression at each concentration, the concentration of modified oligonucleotide that suppresses 50% of gene expression, IC 50 can be calculated.

[0348] RNA isolation RNA analysis can be performed on total cellular RNA or poly(A)+mRNA. Methods of RNA isolation are well known in the art. RNA is prepared using methods well known in the art, for example, using TRIZOL® Reagent (Invitrogen, Carlsbad, CA) according to the manufacturer's recommended protocol.

[0349] Analysis of inhibition of target levels or expression The inhibition of DUX4 nucleic acid level or expression can be assayed by various methods known in the art.For example, the target nucleic acid level can be quantified, for example, by Northern blot analysis, competitive polymerase chain reaction (PCR) or quantitative real-time PCR.RNA analysis can be performed on total cellular RNA or poly(A)+mRNA.The method of RNA isolation is well known in the art.Northern blot analysis is also routine in the art.Quantitative real-time PCR can be conveniently achieved using the commercially available ABI PRISM® 7600, 7700 or 7900 sequence detection system, available from PE-Applied Biosystems, Foster City, CA, and used according to the manufacturer's instructions.

[0350] Quantitative real-time PCR analysis of target RNA levels Quantification of target RNA levels can be achieved by quantitative real-time PCR using the ABI PRISM® 7600, 7700 or 7900 sequence detection system (PE-Applied Biosystems, Foster City, Calif.) according to the manufacturer's instructions. Methods of quantitative real-time PCR are well known in the art.

[0351] Prior to real-time PCR, the isolated RNA is subjected to a reverse transcriptase (RT) reaction, which generates complementary DNA (cDNA) that is then used as a substrate for real-time PCR amplification. The RT and real-time PCR reactions are carried out sequentially in the same sample well. The RT and real-time PCR reagents are obtained from Invitrogen (Carlsbad, CA). The RT and real-time PCR reactions are carried out by methods well known to those skilled in the art.

[0352] The amount of gene (or RNA) target obtained by real-time PCR is normalized using the expression level of a gene with constant expression, such as Cyclophilin A, or by quantifying total RNA using RIBOGREEN® (Invitrogen, Inc. Carlsbad, CA). Cyclophilin A expression is quantified by real-time PCR, either simultaneously with the target, multiplexed or separately. Total RNA is quantified using RIBOGREEN® RNA quantification reagent (Invitrogen, Inc. Eugene, OR). The method of RNA quantification by RIBOGREEN® is taught in Jones, LJ, et al, (Analytical Biochemistry, 1998, 265, 368-374). RIBOGREEN® fluorescence is measured using a CYTOFLUOR® 4000 instrument (PE Applied Biosystems).

[0353] Probes and primers are designed to hybridize to DUX4 nucleic acids. Methods for designing probes and primers for real-time PCR are well known in the art and can include the use of software such as PRIMER EXPRESS® software (Applied Biosystems, Foster City, Calif.).

[0354] Protein level analysis Antisense inhibition of DUX4 nucleic acid can be evaluated by measuring the level of DUX4 protein.The level of DUX4 protein can be examined or quantified by various methods known in the art, such as immunoprecipitation, Western blot analysis (immunoblotting), enzyme-linked immunosorbent assay (ELISA), quantitative protein assay, protein activity assay (e.g., caspase activity assay), immunohistochemistry, immunocytochemistry, or fluorescence-activated cell sorting (FACS).Antibodies against targets can be identified and obtained from various sources, such as the MSRS catalog of antibodies (AerieCorporation, Birmingham, MI), or can be prepared by conventional monoclonal or polyclonal antibody production methods known in the art.

[0355] Gene expression analysis The level of DUX4 gene expression can also be measured using a reporter gene such as luciferase. For example, by using the psiCHECK-2 vector (Promega), the expression of the DUX4 gene can be measured by the amount of luminescence from Renilla luciferase, a fusion protein with DUX4, and the effects of nonspecific cell death can be excluded by correcting for the amount of luminescence from Firefly luciferase present on the same vector.

[0356] In vivo testing of modified oligonucleotides Modified oligonucleotides are tested in animals to assess their ability to inhibit DUX4 expression and alter phenotype. Testing can be performed in normal animals or in experimental disease models, such as transgenic mouse models of DUX4 (Jones,T.et al. PLoS One. 2018;13(2), Article number e0192657) or mice expressing the DUX4 gene using recombinant AAV viruses (Wallace,LM et al. Mol Ther. 2012;20(7):1417, Wallace,LM et al. Ann Neurol. 2011;69(3):540).

[0357] For administration to animals, modified oligonucleotides are formulated in a pharma- ceutically acceptable diluent, such as phosphate buffered saline. Administration includes parenteral administration. Following a period of treatment with modified oligonucleotides, RNA is isolated from tissues to measure changes in DUX4 nucleic acid expression. Changes in DUX4 protein levels are also measured.

[0358] A type of antisense mechanism FSHD is caused by abnormal expression of the DUX4 gene (especially splicing variants of DUX4-FL) in muscle. Meanwhile, DUX4 is also expressed in healthy individuals, for example, in the testes. In addition to DUX4-FL, splicing variants of exon 1, exon 2, exon 6, and exon 7, and splicing variants of exon 1, exon 2, exon 4, exon 5, exon 6, and exon 7 are expressed in certain DUX4 splicing variants expressed in the testes (Non-Patent Document 1).

[0359] Certain biomarkers At least in part, the expression of genes such as MBD3L2, ZSCAN4, TRIM43, DEFB103, and ZNF217 is regulated by the accumulation level of DUX4 protein (Non-Patent Document 2). Creatine kinase in the blood can be measured as a marker for muscle damage.

[0360] Certain indications In certain embodiments, provided herein are methods of treating an individual comprising administering one or more pharmaceutical compositions described herein. In certain embodiments, the individual has FSHD.

[0361] Thus, provided herein is a method for improving symptoms associated with FSHD in a subject in need thereof. In certain embodiments, a method for reducing the incidence of one or more symptoms associated with FSHD is provided. In certain embodiments, a method for reducing the severity of symptoms associated with FSHD is provided. In certain embodiments, symptoms associated with FSHD include muscle stiffness, myotonia, facial muscle weakness, ptosis, inability to whistle, reduced facial expression changes, depressed or angry facial expression, difficulty in pronouncing words, scapular muscle weakness (deformations such as winged scapula, round shoulder, etc.), lower limb weakness, hearing loss, and heart disease.

[0362] In certain embodiments, the methods of the invention comprise administering to an individual in need thereof a therapeutically effective amount of a compound that targets a DUX4 nucleic acid.

[0363] In certain embodiments, administration of a modified oligonucleotide targeted to a DUX4 nucleic acid results in a reduction in expression of DUX4 by at least about 15%, at least about 20%, 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 95% or at least about 99%, or a range defined by any two of these values.

[0364] In certain embodiments, pharmaceutical compositions comprising modified oligonucleotides targeted to DUX4 are used to prepare a medicament for treating a patient suffering from or susceptible to a DUX4-related disease, such as FSHD.

[0365] In certain embodiments, the methods described herein comprise administering a compound comprising a modified oligonucleotide having a consecutive nucleobase portion as described herein, of a sequence set forth in SEQ ID NOs: 2, 3, 4, 7-64, 69-97 or 102-112 of the Sequence Listing.

[0366] Administration In certain embodiments, the compounds and pharmaceutical compositions described herein are administered parenterally.

[0367] In certain embodiments, parenteral administration is by infusion. Infusion may be chronic or continuous, short term or intermittent. In certain embodiments, the infused pharmaceutical agent is delivered by a pump. In certain embodiments, parenteral administration is by injection (e.g., bolus injection). Injectables may be delivered by a syringe.

[0368] Parenteral administration includes, for example, subcutaneous, intravenous, intramuscular, intraarterial, intraperitoneal or intracranial, e.g., intrathecal or intraventricular, administration. Administration may be continuous or long-term, short-term or intermittent.

[0369] In certain embodiments, delivery of a compound of the pharmaceutical compositions described herein results in at least 70% downregulation of target mRNA and / or target protein levels. In certain embodiments, delivery of a compound or composition described herein results in at least 1 day, at least 3 days, at least 5 days, at least 7 days, at least 10 days, at least 14 days, at least 20 days, at least 21 days, at least 28 days, at least 30 days, at least 35 days, at least 40 days, at least 45 days, at least 50 days, at least 55 days, at least 60 days, at least 65 days, at least 70 days, at least 75 days, at least 76 days, at least 77 days, , resulting in a 10%, 20%, 30%, 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% downregulation of target mRNA and / or target protein levels for at least 78 days, at least 79 days, at least 80 days, at least 85 days, at least 90 days, at least 95 days, at least 100 days, at least 105 days, at least 110 days, at least 115 days, at least 120 days, or at least 1 year.

[0370] In certain embodiments, the modified oligonucleotide is delivered by injection or infusion once daily, once every three days, once weekly, once every other week, once every three weeks, once every month, once every two months, once every three months, once every six months, twice a year, or once a year.

[0371] Certain combination therapies In certain embodiments, the first agent comprising the modified oligonucleotide of the present invention is co-administered with one or more second agents. In certain embodiments, such second agents are designed to treat the same FSHD as the first agent described herein. In certain embodiments, such second agents are designed to treat a different disease, disorder or condition than the first agent described herein. In certain embodiments, such second agents are designed to treat the undesirable side effects of one or more pharmaceutical compositions described herein. In certain embodiments, the second agent is co-administered with the first agent to treat the undesirable effects of the first agent. In certain embodiments, the second agent is co-administered with the first agent to produce a combined effect. In certain embodiments, the second agent is co-administered with the first agent to produce a synergistic effect.

[0372] In certain embodiments, the first agent and the one or more second agents are administered simultaneously. In certain embodiments, the first agent and the one or more second agents are administered at different times. In certain embodiments, the first agent and the one or more second agents are prepared together in a single pharmaceutical formulation. In certain embodiments, the first agent and the one or more second agents are prepared separately.

[0373] Certain compounds In certain embodiments, the compounds disclosed herein can be synthesized into oligomers by the phosphoramidite method using commercially available amidites (including LNA) for DNA and RNA synthesis. The artificial nucleic acid GuNA can be synthesized into oligomers by the methods described in WO2014 / 046212 and WO2017 / 047816. The artificial nucleic acids ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Trz], and ALNA[Oxz] can be synthesized into oligomers by the methods described in Japanese Patent Application No. 2018-212424.

[0374] In certain embodiments, the compounds disclosed herein benefit from one or more improved in vitro and / or in vivo properties as compared to a suitable comparator compound.

[0375] In certain embodiments, the compound is Compound No. 1 having the sequence (5' to 3') ngagattcccgccggt (where n is 5-methylcytosine, incorporated herein as SEQ ID NO:2), i.e., a gapmer in which the 5' wing and the 3' wing are composed of three LNA-containing nucleosides, and each internucleoside linkage is a phosphorothioate linkage.

[0376] In certain embodiments, the compound is Compound No. 2 having the sequence (5' to 3') gnagttctccgcggt (where n is 5-methylcytosine, incorporated herein as SEQ ID NO: 3 in the Sequence Listing), i.e., a gapmer in which the 5' wing and the 3' wing are each composed of three ALNA[Ms]-containing nucleosides, and each internucleoside linkage is a phosphorothioate linkage.

[0377] In certain embodiments, the compound is Compound No. 3 having the sequence (5' to 3') gnntagacagcgtngg (where n is 5-methylcytosine, incorporated herein as SEQ ID NO: 4 in the Sequence Listing), i.e., a gapmer in which the 5' wing and the 3' wing are each composed of three LNA-containing nucleosides, and each internucleoside linkage is a phosphorothioate linkage.

[0378] In certain embodiments, the compound is Compound No. 123 having the sequence (5' to 3') gnntagacagcgtngg (where n is 5-methylcytosine, incorporated herein as SEQ ID NO: 4 in the Sequence Listing), i.e., a gapmer in which the 5' wing and the 3' wing are composed of three ALNA[Ms]-containing nucleosides, and each internucleoside linkage is a phosphorothioate linkage.

[0379] Non-Limiting Disclosure and Incorporation by Reference While certain compounds, compositions and methods described herein are specifically described in accordance with certain embodiments, the following examples serve merely to illustrate the compounds described herein and are not intended to be limiting thereof. Each of the references, GENBANK Accession Numbers, etc. described in this application are incorporated herein by reference in their entirety.

[0380] Although the sequence listing accompanying this application identifies each sequence as either "RNA" or "DNA" as appropriate, in practice the sequences may be modified with any combination of chemical modifications. Those of skill in the art will readily appreciate that designations such as "RNA" or "DNA" to describe modified oligonucleotides are, in some cases, arbitrary. For example, an oligonucleotide comprising a nucleoside containing a 2'-OH sugar moiety and a thymine base may be described as a DNA with a modified sugar (2'-OH as opposed to the natural 2'-H of DNA) or an RNA with a modified base (thymine (methylated uracil) as opposed to the natural uracil of RNA).

[0381] Thus, the nucleic acid sequences provided herein, including but not limited to those in the sequence listing, are intended to encompass nucleic acids comprising any combination of natural or modified RNA and / or DNA, including but not limited to those nucleic acids having modified nucleobases. As a further non-limiting example, an oligomeric compound having the nucleobase sequence "ATCGATCG" encompasses any oligomeric compound having such a nucleobase sequence, whether modified or unmodified, including but not limited to those compounds containing RNA bases, such as those having the sequence "AUCGAUCG", as well as those having some DNA bases and some RNA bases, such as "AUCGATCG", and oligomeric compounds having other modified or naturally occurring bases, such as "ATmeCGAUCG" (where meC represents a cytosine base containing a methyl group at the 5-position). EXAMPLES

[0382] NON-LIMITING DISCLOSURE AND INCORPORATION BY REFERENCE While certain compounds, compositions and methods described herein are specifically described in accordance with certain embodiments, the following examples serve only to illustrate the compounds described herein and are not intended to be limiting thereof. Each of the references described in this application is incorporated herein by reference in its entirety.

[0383] The structure of each artificial nucleic acid used in the present specification is shown in the following structural formula together with its abbreviation. Structure and abbreviation of each artificial nucleic acid [ka]

[0384] Example 1 Synthesis and purification of modified oligonucleotide compounds for in vitro evaluation Modified oligonucleotide compounds were synthesized using various amidites (LNA amidites were purchased from Chem Genes and Hongene Biotechnology Limited, 2'-OMe amidites were purchased from Sigma-Aldrich, GuNA was synthesized by the methods described in WO2014 / 046212 and WO2017 / 047816, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Trz] and ALNA[Oxz] were synthesized by the methods described in Japanese Patent Application No. 2018-212424) on a 0.2 or 1.0 μmol scale using a DNA / RNA oligonucleotide automatic synthesizer nS-8II (Gene Design Co., Ltd.) on a CPG or polystyrene support. All amidites were adjusted to 0.1 M acetonitrile solution, and the coupling time for unnatural nucleosides was 10 minutes, with the other steps being carried out under standard conditions for nS-8II. Activator 42 (Sigma-Aldrich) was used as the activator, and Sulfurizing Reagent II (Gren Research Corporation) was used for thiolation. The synthesized oligonucleotides were cleaved from the support and deprotected by adding 28% aqueous ammonia and reacting at 60-65°C for 8 hours. After concentrating and distilling off the ammonia, the oligonucleotides were purified by reversed-phase HPLC.

[0385] Example 2 Synthesis and purification of modified oligonucleotide compounds for in vivo evaluation Modified oligonucleotide compounds were synthesized using various amidites on a polystyrene support at a 20-50 μmol scale using a DNA / RNA oligonucleotide automatic synthesizer AKTA oligopilot plus 10 (GE Healthcare Japan Co., Ltd.). DNA amidites were adjusted to 0.1 M, and non-natural amidites were adjusted to 0.05-0.1 M acetonitrile solutions. The coupling recycle time for non-natural nucleosides was 20 minutes, and when introducing the first base into the universal support, the coupling, thiolation, and capping steps were each performed twice in succession. Other steps were performed under the standard conditions of AKTA oligopilot plus10. Activator42 (Sigma-Aldrich) was used as the activator, and Sulfurizing Reagent II (Gren Research Corporation) was used for thiolation. The synthesized oligonucleotides were decyanoethylated on the solid phase using 20% ​​diethylamine / acetonitrile or 50% triethylamine / acetonitrile, and then cleaved from the support and deprotected at the base moiety by adding 28% aqueous ammonia and reacting at 60-65°C for 8-24 hours. After concentrating and distilling off the ammonia, the oligonucleotides were purified using an anion exchange column. Excess salts contained after anion exchange were removed using a desalting column.

[0386] Example 3 Purity check of modified oligonucleotide compounds The purified and purified oligonucleotides were determined by reverse phase HPLC under the following conditions. The purity of each compound was 85% or higher. Reverse phase HPLC (purification) Mobile phase: Solution A: 400 mM hexafluoroisopropanol, 15 mM triethylamine Liquid B: Methanol Gradient: A:B =85:15→70:30(10min) Columns used: Preparative Waters XBridge@ Oligonucleotide BEH C18 OBDTM Prep Column,130Å,2.5μm,10mm*50mm Flow rate: Preparative 5mL / min Column temperature: 60℃ Detection: UV (260 nm) Reverse phase HPLC (purity confirmation) Mobile phase: Solution A: 400 mM hexafluoroisopropanol, 15 mM triethylamine aqueous solution Liquid B: Methanol Gradient: A:B = 80:20 → 70:30 (6.5 min) Columns used: Analysis Waters ACQUITY UPLC@ Oligonucleotide BEH C18 Column, 130Åm 1.7μm, 2.1mm*50mm Flow rate: 0.2mL / min Column temperature: 60℃ Detection: UV (260 nm) Anion exchange purification Mobile phase: Solution A: 1 mM NaOH 20% acetonitrile solution Solution B: 1mM NaOH, 1.5M NaCl / 20% acetonitrile aqueous solution Column used: TSKgel SuperQ-5PW(13) φ21.1*15mm Flow rate: 7mL / min Column temperature: room temperature Detection: UV (260 nm) Desalting Column Mobile phase: Solution A: 20% acetonitrile solution Solution B: 20% acetonitrile aqueous solution Columns used: GE HiPrep 26 / 10 Desalting*4 in series Flow rate: 12mL / min Column temperature: room temperature

[0387] Example 4 Molecular weight measurement of modified oligonucleotide compounds The molecular weight of the synthesized modified oligonucleotide compound was measured using Waters ZQ under the following conditions. Mobile phase: Solution A: 400 mM hexafluoroisopropanol, 15 mM triethylamine aqueous solution Liquid B: Methanol Gradient: A:B = 80:20 → 70:30 (6.5 min) Columns used: Waters ACQUITY UPLC@ Oligonucleotide BEH C18 Column, 130Åm 1.7μm, 2.1mm*50mm Flow rate: 0.2mL / min Column temperature: 60℃ Detection: UV (260 nm)

[0388] Example 5 Molecular weight of the synthesized modified oligonucleotide compounds The synthesized modified oligonucleotide compounds are shown in Table 1. Each nucleotide in the compound is represented by three letters, except for the 3'-terminal nucleotide, which is represented by two letters since it has no internucleoside bond. 1) The first letter is capitalized and represents the following nucleobase: A=adenine, T=thymine, G=guanine, C=cytosine, U=uracil, M=5-methylcytosine, 2) The second letter represents the sugar moiety: l = LNA, g = GuNA, m = ALNA [Ms], u = ALNA [mU], p = ALNA [ipU], t = ALNA [Trz], e = 2'-MOE, o = 2'-OMe, d = 2'-deoxyribose, 3) The third letter represents the internucleoside bond: s=phosphorothioate, p=phosphodiester. The target position is shown as the 5' target site of the modified oligonucleotide in DUX4 mature mRNA (the position of SEQ ID NO: 1 in the sequence listing corresponding to the 3' end of the modified oligonucleotide). [Table 1-1] [Table 1-2] [Table 1-3] [Table 1-4] [Table 1-5] [Table 1-6]

[0389] Example 6 In vitro DUX4 knockdown activity test (Lipofection method) C2C12 cells were transfected onto a mixture of DUX4-modified oligonucleotides and Lipofectamine RNAi Reagent at 1.25 × 10 4 cells / cm 2The cells were seeded so that the total number of cells was 100, and cultured overnight in a CO2 incubator. The next day, the cells were transfected with a reporter plasmid in which the DUX4 sequence was cloned into the multicloning site of the psiCHECK-2 vector (Promega) using Lipofectamine 2000 Reagent, and cultured in a CO2 incubator for about 24 hours. After that, the luminescence values ​​of Firefly luciferase and Renilla luciferase in the cells were detected with a plate reader using the Dual-Glo Luciferase Assay System. To correct the effects of transfection efficiency and cell number from the luminescence value due to Renilla luciferase activity, the ratio to the luminescence value due to Firefly luciferase activity was calculated. The inhibition rate was calculated as a percentage from the reduction rate of Renilla / Firefly when the modified oligonucleotide was added, and the IC was calculated from the two concentrations that sandwiched 50% and the inhibition rate at that time. 50 The values ​​were calculated (Table 2). Compared with the compounds (compound numbers 1 to 132) that are complementary to positions 232 to 248, 1306 to 1325, or 1472 to 1495 of DUX4 mature mRNA, compound numbers 133 (complementary to positions 214 to 227 of SEQ ID NO: 1 in the sequence listing), 134 (complementary to positions 1323 to 1336 of SEQ ID NO: 1 in the sequence listing), 135 (complementary to positions 1458 to 1471 of SEQ ID NO: 1 in the sequence listing), and 136 (complementary to positions 1495 to 1508 of SEQ ID NO: 1 in the sequence listing) were found to have significantly weaker inhibition rates.

[0390] Example 7 In vitro DUX4 knockdown activity test (Gymnosis method) DUX4-modified oligonucleotide solution was added to 6 x 10 C2C12 cells. 3 cells / cm 2The cells were seeded so that the total volume was 100 μg / ml and cultured in a CO2 incubator for 2 nights. After 2 days, the medium containing the DUX4 modified oligonucleotide solution was removed from the cells, and the cells were washed with new medium. Then, using Lipofectamine 2000 Reagent, a reporter plasmid in which the DUX4 sequence was cloned into the multicloning site of the psiCHECK-2 vector (Promega) was transfected into the cells, and the cells were cultured in a CO2 incubator for about 24 hours. Then, using the Dual-Glo Luciferase Assay System, the luminescence values ​​of Firefly luciferase and Renilla luciferase in the cells were detected with a plate reader. In order to correct the effects of transfection efficiency and cell number from the luminescence value due to Renilla luciferase activity, the ratio to the luminescence value due to Firefly luciferase activity was calculated. The inhibition rate was calculated as a percentage from the reduction rate of Renilla / Firefly when the modified oligonucleotide was added, and the IC was calculated from the two concentrations that sandwiched 50% and the inhibition rate at that time. 50 The values ​​were calculated. The results are shown in Table 2 below. Compared with the compounds (compound numbers 1 to 132) containing nucleic acid base sequences complementary to the isometric portion in the region of positions 232 to 248, 1306 to 1325, or 1472 to 1495 of DUX4 mature mRNA, compound numbers 133 (complementary to positions 214 to 227 of SEQ ID NO: 1 in the sequence listing), 134 (complementary to positions 1323 to 1336 of SEQ ID NO: 1 in the sequence listing), 135 (complementary to positions 1458 to 1471 of SEQ ID NO: 1 in the sequence listing), and 136 (complementary to positions 1495 to 1508 of SEQ ID NO: 1 in the sequence listing) were found to have significantly weaker inhibition rates. [Table 2-1] [Table 2-2] [Table 2-3] [Table 2-4]

[0391] Example 8 Synthesis of modified oligonucleotide compounds and in vitro DUX4 knockdown activity test (Gymnosis method) Table 3 shows newly synthesized modified oligonucleotide compounds and the results of an in vitro DUX4 knockdown activity test performed in the same manner as in Example 7 for the compounds.

[0392] In Table 3, each nucleotide is represented by three letters, except for the 3'-terminal nucleotide, which is represented by two letters since it has no internucleoside bond. 1) The first letter is capitalized and represents the following nucleobase: A=adenine, T=thymine, G=guanine, C=cytosine, U=uracil, M=5-methylcytosine, 2) The second letter represents the sugar moiety: l = LNA, m = ALNA [Ms], e = 2'-MOE, o = 2'-OMe, d = 2'-deoxyribose, 3) The third letter represents the internucleoside bond: s=phosphorothioate, p=phosphodiester. The target position is shown as the 5' target site of the modified oligonucleotide in DUX4 mature mRNA (the position of SEQ ID NO: 1 in the sequence listing corresponding to the 3' end of the modified oligonucleotide).

[0393] Compared with the compounds (compound numbers 137 to 247) containing nucleic acid base sequences complementary to equal-length portions within the regions of positions 126 to 147, 232 to 248, 1306 to 1325, or 1472 to 1495 of DUX4 mature mRNA, compound numbers 248 (complementary to positions 112 to 127 of SEQ ID NO: 1 in the Sequence Listing), 249 (complementary to positions 162 to 177 of SEQ ID NO: 1 in the Sequence Listing), 250 (complementary to positions 264 to 279 of SEQ ID NO: 1 in the Sequence Listing), and 251 (complementary to positions 1273 to 1288 of SEQ ID NO: 1 in the Sequence Listing) were found to have significantly weaker inhibition rates.

[0394] Table 3 [Table 3-1]

[0395] Table 3. Continued [Table 3-2]

[0396] Example 9 In vivo DUX4 knockdown activity assay An adeno-associated virus vector AAV-DUX4 (SignaGen Laboratories, Cat.#SL100862) incorporating DUX4 mature mRNA of sequence number 1 in the sequence table was produced. AAV-DUX4 was intramuscularly administered at 1E+10VG / 50 μL to the tibialis anterior muscle of an 8-week-old C57BL / 6J mouse (male, Charles River, Japan) under isoflurane (Pfizer Inc.) anesthesia. Three days later, modified oligonucleotides targeting DUX4 were prepared in saline at 1, 3, 10 and 50 mg / 5 mL / kg and administered into the tail vein of an 8-week-old C57BL / 6J mouse (male, Charles River, Japan). After 72 hours, whole blood was collected from the abdominal vena cava under cervical dislocation or isoflurane (Pfizer Inc.) anesthesia, and the mouse was killed. After sacrifice, the tibialis anterior muscle was collected, immersed in RNAlater Soln. (Invitrogen), and then frozen at -80°C. The tissue was added with homogenization buffer from Maxwell RSC simplyRNA Tissue Kit (Promega), disrupted using a multi-beads shocker, and RNA was purified according to the protocol described in the kit. 400 ng of RNA was reverse transcribed, and quantitative PCR was performed using the obtained cDNA. The knockdown activity of the modified oligonucleotide was shown as the quantitative ratio of DUX4 to 18S rRNA relative to the vehicle group. The results for 1, 3, 10, and 50 mg / 5 mL / kg are shown in Figures 1 to 4.Compound No. 1 (complementary sequence to positions 233 to 248 of DUX4 mature mRNA), Compound No. 2 (complementary sequence to positions 1309 to 1323 of DUX4 mature mRNA), Compound No. 3 (complementary sequence to positions 1480 to 1495 of DUX4 mature mRNA), Compound No. 13 (complementary sequence to positions 234 to 247 of DUX4 mature mRNA), Compound No. 41 (complementary sequence to positions 1308 to 1323 of DUX4 mature mRNA), Compound No. 54 (complementary sequence to positions 1309 to 1323 of DUX4 mature mRNA), Compound No. 57 (complementary sequence to positions 130 of DUX4 mature mRNA), Compound No. 68 (complementary sequence to positions 1309 to 1323 of DUX4 mature mRNA), compound No. 78 (complementary sequence to positions 1309 to 1324 of DUX4 mature mRNA), compound No. 88 (complementary sequence to positions 1310 to 1323 of DUX4 mature mRNA), compound No. 104 (complementary sequence to positions 1473 to 1488 of DUX4 mature mRNA), and compound No. 122 (complementary sequence to positions 1480 to 1495 of DUX4 mature mRNA) were able to suppress DUX4 gene expression in muscle when administered to the body.

[0397] Example 10 Safety of modified oligonucleotides When compounds Nos. 3, 42, and 123 were intravenously administered to 6-week-old ICR mice (male, Charles River, Japan) at a maximum dose of 100 mg / kg, no findings such as hepatotoxicity (increase in ALT and AST in the blood, and abnormal histopathological findings), nephrotoxicity (increase in UN and creatinine in the blood, and abnormal histopathological findings), changes in general symptoms, or death were observed.

[0398] Example 11 In vivo Tg mouse DUX4 knockdown activity test Nine-week-old male FLExDUX4-heteto / HSA-MCM-hetero:TG (DUX4-Tg) and FLExDUX4-wild / HSA-MCM-hetero:TG (MCM, control) mice were used (male, introduced from The Jackson Laboratory to Charles River Japan, Inc.). Modified oligonucleotides targeting DUX4 were prepared with saline at 5 mL / kg for each dose and administered into the tail vein once a week. One week after the end of the four-week administration, whole blood was collected from the abdominal vena cava under deep isoflurane anesthesia, and the mice were euthanized. EDTA plasma was separated and used for creatine kinase (CK) measurement. Lower limb muscles were collected, wet weights were measured, and gene expression analysis was performed. As shown in Figures 5 and 6, Compound No. 3 and Compound No. 123 suppressed DUX4 mRNA expression. They also reduced the blood level of CK, a muscle disorder marker. On the other hand, Compound No. 113 and Compound No. 247 did not show any clear effect on DUX4 mRNA expression or blood CK level.

[0399] Example 12 Repeated administration toxicity test in mice Modified oligonucleotides targeting DUX4 were prepared in saline at 100 mg / 5 mL / kg and administered to 6-week-old ICR mice (male, Charles River, Japan) via the tail vein for 4 consecutive days. 72 hours after the final administration, blood was collected from the posterior vena cava under isoflurane anesthesia, and clinical biochemistry tests were performed. After exsanguination, autopsy was performed, and histopathological examination of the liver and kidney was performed. Compound No. 123 did not cause death or change in general condition, food intake, or body weight after administration, and no hepatotoxicity (increase in serum ALT and AST, and abnormal histopathological findings) or nephrotoxicity (increase in serum UN and creatinine, and abnormal histopathological findings) was observed. On the other hand, for compound No. 113 and compound No. 247, although no deaths or changes in general condition, food intake or body weight were observed after administration, clear hepatotoxicity (increases in serum ALT, AST, GLDH, ALP, bilirubin, bile acid, histopathological abnormal findings: hepatocellular degeneration and necrosis, hepatocellular hypertrophy) and nephrotoxicity (increases in serum creatinine) were observed in both. In addition, the liver and kidney concentrations of compound No. 123 under the test conditions were 323 and 251 μg / g, respectively, which were equivalent or higher than the liver and kidney concentrations of compound No. 247 (111 and 185 μg / g) and compound No. 113 (39.3 and 235 μg / g), but no liver or kidney toxicity was observed.

[0400] [Table 4]

[0401] [Table 5]

[0402] Reference example The synthesis schemes of ALNA[Ms]-containing nucleotides, ALNA[mU]-containing nucleotides, ALNA[ipU]-containing nucleotides, ALNA[Trz]-containing nucleotides, and ALNA[Oxz]-containing nucleotides are shown below. Starting compounds 1a, 1d, and 1g can be synthesized by the method described in International Publication No. 2017 / 047816.

[0403] Synthesis of ALNA[Ms]-T [ka]

[0404] Synthesis of ALNA[Ms]-mC [ka]

[0405] Synthesis of ALNA[Ms]-G [ka]

[0406] Synthesis of ALNA[Ms]-A [ka]

[0407] Synthesis of ALNA[mU]-T [ka]

[0408] Synthesis of ALNA[mU]-mC [ka]

[0409] Synthesis of ALNA[mU]-G [ka]

[0410] Synthesis of ALNA[mU]-A [ka]

[0411] Synthesis of ALNA[ipU]-T [ka]

[0412] Synthesis of ALNA[ipU]-mC [ka]

[0413] Synthesis of ALNA[ipU]-G [ka]

[0414] Synthesis of ALNA[ipU]-A [ka]

[0415] Synthesis of ALNA[Trz]-T [ka]

[0416] Synthesis of ALNA[Trz]-mC [ka]

[0417] Synthesis of ALNA[Trz]-G [ka]

[0418] Synthesis of ALNA[Trz]-A [ka]

[0419] Synthesis of ALNA[Oxz]-T [ka]

[0420] Synthesis of ALNA[Oxz]-mC [ka] [Industrial Applicability]

[0421] The modified oligonucleotides of the present invention can be used as compounds useful for treating, preventing, or slowing the progression of DUX4-related diseases.

[0422] [Sequence table free text] SEQ ID NO:1 in the sequence listing shows the nucleotide sequence of DUX4 mature mRNA. SEQ ID NOs: 2 to 4 and 7 to 112 in the sequence listing show the base sequences of modified oligonucleotides. SEQ ID NOs: 5 and 6 in the sequence listing show the base sequences of DUX4-FL2 and DUX4-s, which are splicing variants of SEQ ID NO:1.

Claims

1. A modified oligonucleotide consisting of 15 to 30 residues, a sequence of at least 15 consecutive nucleobases that is complementary to an equal length portion of positions 126-147, 1306-1325, or 1480-1495 from the 5' end of the nucleobase sequence of the mature mRNA of DUX4 of SEQ ID NO:1; the nucleobase sequence of said modified oligonucleotide has at least 90% complementarity to an equal length portion of the nucleobase sequence of the mature mRNA of DUX4 of SEQ ID NO:1; When the at least 15 contiguous nucleobase sequence comprises a nucleobase sequence that is complementary to an equal length portion of the nucleobase sequence of SEQ ID NO: 1 at positions 1480 to 1495 from the 5' end, the modified oligonucleotide consists of a nucleobase sequence having at its 3' end the complementary base of the nucleobase sequence of SEQ ID NO: 1 at position 1480 from the 5' end. Modified oligonucleotides.

2. The modified oligonucleotide of claim 1 , wherein one or more modified nucleotides of the modified oligonucleotide comprises a modified sugar.

3. 3. The modified oligonucleotide of claim 2, wherein the modified sugar is selected from the group consisting of a bicyclic sugar, a 2'-O-methoxyethyl modified sugar, and a 2'-O-methyl modified sugar.

4. 4. The modified oligonucleotide of claim 3, wherein the bicyclic sugar is selected from the group consisting of LNA, GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz], and ALNA[Trz].

5. A modified oligonucleotide consisting of 15 to 30 residues, a sequence of at least 15 consecutive nucleobases that is complementary to an equal length portion of the nucleobase sequence of DUX4 mature mRNA from positions 1472 to 1495 from the 5' end of SEQ ID NO:1; the nucleobase sequence of said modified oligonucleotide has at least 90% complementarity to an equal length portion of the nucleobase sequence of the mature mRNA of DUX4 of SEQ ID NO:1; the modified oligonucleotide is selected from GuNA, ALNA[Ms], ALNA[mU], ALNA[ipU], ALNA[Oxz], and ALNA[Trz]; At least one nucleoside comprising Modified oligonucleotides.

6. 6. The modified oligonucleotide of claim 5, wherein the modified oligonucleotide further comprises a 2'-O-methoxyethyl modified sugar and / or a 2'-O-methyl modified sugar.

7. The modified oligonucleotide of any one of claims 1 to 6, wherein at least one modified nucleotide of the modified oligonucleotide comprises a modified nucleobase.

8. The modified oligonucleotide of claim 7, wherein the modified nucleobase is 5-methylcytosine.

9. The modified oligonucleotide of any one of claims 1 to 8, wherein at least one internucleoside linkage is a modified internucleoside linkage.

10. 10. The modified oligonucleotide of claim 9, wherein the modified internucleoside linkage is a phosphorothioate internucleoside linkage.

11. the modified oligonucleotide comprising: 1) a gap segment; 2) a 5' wing segment; and 3) a 3' wing segment; the gap segment is positioned between the 5' wing segment and the 3' wing segment; each of the 5' wing segments and the 3' wing segments comprises at least one modified sugar; the nucleosides of the gap segment are either all nucleosides that do not contain a modified sugar or they are all nucleosides that contain one or two nucleosides that contain a modified sugar and the rest that do not contain a modified sugar; The modified oligonucleotide according to any one of claims 1 to 10.

12. Below formula: GlsMlsMlsTdsAdsGdsAdsCdsAdsGdsCdsGdsTdsMlsGlsGl; A modified oligonucleotide, represented by: During the ceremony, Each nucleobase has the following symbol: A = adenine, T = thymine, G = guanine, C = cytosine, M = 5-methylcytosine, As indicated according to; Each sugar moiety has the following symbol: l=LNA, d=2′-deoxyribose, As indicated according to; Each internucleoside bond has the following symbol: Designated accordingly: s = phosphorothioate.

13. Below formula: GmsMmsMmsTdsAdsGdsAdsCdsAdsGdsCdsGdsTdsMmsGmsGm; A modified oligonucleotide, represented by: During the ceremony, Each nucleobase has the following symbol: A = adenine, T = thymine, G = guanine, C = cytosine, M = 5-methylcytosine, As indicated according to; Each sugar moiety has the following symbol: m = ALNA [Ms], d = 2'-deoxyribose, As indicated according to; Each internucleoside bond has the following symbol: Designated accordingly: s = phosphorothioate.

14. Below formula: GmsMmsAmsGdsTdsTdsCdsTdsCdsCdsGdsCdsGmsGmsTm; A modified oligonucleotide, represented by: During the ceremony, Each nucleobase has the following symbol: A = adenine, T = thymine, G = guanine, C = cytosine, M = 5-methylcytosine, Thus, it is shown; Each sugar moiety has the following symbol: m = ALNA [Ms], d = 2'-deoxyribose, As indicated according to; Each internucleoside bond has the following symbol: s = phosphorothioate As shown in accordance with

15. Below formula: 【Chemistry 1】 A modified oligonucleotide or a salt thereof, represented by:

16. Below formula: 【Chemistry 2】 A modified oligonucleotide or a salt thereof, represented by:

17. Below formula: 【Chemistry 3】 A modified oligonucleotide or a salt thereof, represented by:

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