CBP / catenin inhibitor treatment regimen for liver fibrosis

Abstract

[Problem] To provide a pharmaceutical composition useful for the prevention or treatment of liver disease, in particular, liver fibrosis or liver cirrhosis. [Solution] Provided is a pharmaceutical composition that is for the prevention and / or treatment of liver disease and that contains 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinoline-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazine-6-yl}methyl)phenyl dihydrogen phosphate or a pharmaceutically acceptable salt thereof. The pharmaceutical composition is characterized in that 100 to 400 mg / m2 of the 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinoline-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazine-6-yl}methyl)phenyl dihydrogen phosphate or a pharmaceutically acceptable salt thereof is administered intravenously to a human once or twice a week for 2 to 5 hours each time, and the administration is continued for 2 to 6 months.

Description

[Technical Field]

[0001] The present invention relates to a pharmaceutical composition for preventing and treating liver diseases, particularly liver diseases such as liver fibrosis and liver cirrhosis. [Background technology]

[0002] Chronic organ damage leads to fibrosis in affected tissues, such as the liver, heart, kidneys, and lungs. In the liver, fibrosis is the first step toward cirrhosis, which can lead to liver dysfunction, esophageal varices, and hepatocellular carcinoma (HCC), resulting in over one million deaths annually worldwide. Causes of cirrhosis include hepatic steatosis due to excessive alcohol consumption and overeating, and hepatitis due to viral infections. Treatment options include alcohol abstinence, dietary therapy, and antiviral drugs. Chronic cholestasis and subsequent liver damage and cirrhosis can also be caused by certain medications or specific diseases, such as primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), familial intrahepatic cholangitis, Alagille syndrome, and intrahepatic cholangitis of pregnancy. PBC and PSC are chronic, progressive biliary liver diseases caused by autoimmune disorders of unknown etiology. Currently, there is no effective treatment other than liver transplantation. The prevalence of PBC is 140 cases per million, and the prevalence of PSC is 0-317 cases per million. Bile acidity liver injury results from hepatic parenchymal cell destruction due to the accumulation of hydrophobic bile acids (BAs). Initial hepatocyte damage induces a subsequent inflammatory response, exacerbating hepatocellular and intralobar bile duct damage, leading to fibrosis and ultimately liver failure due to cirrhosis. While ursodeoxycholic acid and bezafibrate are recognized therapeutic agents for PBC, no antifibrotic drugs have yet been developed for the treatment of PBC or PSC-associated cirrhosis (Non-Patent Documents 1 and 2). FXR, its transporter system, and BA receptors such as fibroblast growth factor 19 have attracted attention as therapeutic targets for cholestatic liver disease and liver fibrosis (Non-Patent Documents 3 and 4). However, there are currently no therapeutic agents that can directly reduce BA levels.

[0003] Previous studies have shown that abnormalities in Wnt / β-catenin signaling are involved in fibrosis (Non-Patent Documents 5-7). It has been reported that β-catenin deletion increased liver injury and fibrosis due to cholestasis in Mdr2-KO mice, but suppressed liver injury and fibrosis due to cholestasis in bile duct-ligated mice (Non-Patent Documents 8 and 9).

[0004] 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate (foscenvivint) is known as a small molecule therapeutic agent related to the inhibition of intracellular protein-protein interactions in the Wnt pathway, and this compound has been reported to be useful as a preventive and therapeutic agent for liver fibrosis (Patent Document 1). In addition, this compound has the effect of improving liver function, particularly the decline in liver glucose metabolism, electron transport system function, and hepatic synthetic ability, and is effective as a liver function improver (Patent Document 2). [Prior art documents] [Patent documents]

[0005] [Patent Document 1] Patent No. 6303112 [Patent Document 2] WO2020 / 122022 [Non-patent literature]

[0006] [Non-Patent Document 1] Poupon RE, Poupon R, Balkau B. Ursodiol for the long-term treatment of primary biliary cirrhosis. The UDCA-PBC Study Group. N Engl J Med 330, 1342-1347 (1994). [Non-patent document 2] Corpechot C, et al. A Placebo-Controlled Trial of Bezafibrate in Primary Biliary Cholangitis. N Engl J Med 378, 2171-2181 (2018). [Non-patent document 3] Trauner M, Fuchs CD. Novel therapeutic targets for cholestatic and fatty liver disease. Gut, (2021). [Non-patent document 4] Trauner M, Fuchs CD, Halilbasic E, Paumgartner G. New therapeutic concepts in bile acid transport and signaling for management of cholestasis. Hepatology 65, 1393-1404 (2017). [Non-Patent Document 5] Logan CY, Nusse R. The Wnt signaling pathway in development and disease. Annu Rev Cell Dev Biol 20, 781-810 (2004). [Non-patent document 6] Nusse R. Wnt signaling in disease and in development. Cell Res 15, 28-32 (2005). [Non-Patent Document 7] Zhou L, et al. Multiple Genes of the Renin-Angiotensin System Are Novel Targets of Wnt / beta-Catenin Signaling. J Am Soc Nephrol 26, 107-120 (2015). [Non-patent document 8] Pradhan-Sundd T, et al. Wnt / beta-Catenin Signaling Plays a Protective Role in the Mdr2 Knockout Murine Model of Cholestatic Liver Disease. Hepatology 71, 1732-1749 (2020). [Non-Patent Document 9] Zhang R, et al. Activation of WNT / Beta-Catenin Signaling and Regulation of the Farnesoid X Receptor / Beta-Catenin Complex After Murine Bile Duct Ligation. Hepatol Commun 3, 1642-1655 (2019). Summary of the Invention [Problem to be solved by the invention]

[0007] An object of the present invention is to provide a pharmaceutical composition useful for preventing or treating liver diseases. [Means for solving the problem]

[0008] The following formula:

[0009] [ka]

[0010] The compound represented by the formula (I), 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate (foscenvivint, (also known as foscenvivint, PRI-724, OP-724)), hereinafter also referred to as "the compound of the present disclosure"), is a small molecule therapeutic agent associated with inhibiting intracellular protein-protein interactions in the Wnt pathway, which is essential for regulating cancer stem cells (CSCs). Following an investigator-initiated domestic clinical trial of foscenvivint in Japanese patients with cirrhosis caused by hepatitis B virus or hepatitis C virus, the present inventors initiated domestic investigator-initiated clinical trials in patients with advanced PBC and in patients with cirrhosis caused by co-infection of human immunodeficiency virus associated with hemophilia and hepatitis C virus (hereinafter referred to as hemophilia HIV / HCV co-infection). During this process, the inventors diligently investigated and succeeded in optimizing the dosage and evaluation index of the compound disclosed herein, leading to the completion of the present invention. The present disclosure includes the following features.

[0011] [1]100~400mg / m 2 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human once or twice a week over 2 to 5 hours each time, and the administration is continued for 2 to 6 months. A pharmaceutical composition for preventing and / or treating liver disease, comprising phosphate or a pharmaceutically acceptable salt thereof. [2] 280 mg / m 2 The pharmaceutical composition according to the above-mentioned [1], wherein 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human twice a week over four hours for 12 weeks. [3] The pharmaceutical composition according to [1] or [2] above, wherein the liver disease is accompanied by liver fibrosis or cirrhosis. [4] The pharmaceutical composition according to [3] above, wherein the liver fibrosis or cirrhosis is a disease caused by hepatitis B or C, or primary biliary cholangitis (PBC). [5] The pharmaceutical composition according to [3], wherein the liver fibrosis or cirrhosis is a disease caused by hemophilia, HIV / HCV coinfection, or non-alcoholic steatohepatitis. [6] The pharmaceutical composition described in [3], wherein the liver disease is classified as A, B, or C according to the Child-Pugh score. [7] The pharmaceutical composition according to any one of [1] to [6] above, which is for maintaining or improving liver tissue stiffness. [8] The pharmaceutical composition according to [7] above, wherein the maintenance or improvement is evaluated during or at the end of drug administration compared with the state before the start of drug administration. [9] The pharmaceutical composition according to [7] above, wherein the maintenance or improvement is evaluated 6 to 12 months after the end of drug administration compared with the time at which drug administration ended.

[10] The pharmaceutical composition described in [7] above, wherein liver tissue stiffness is indicated by fibroscan measurement values.

[11] The pharmaceutical composition described in [7], wherein liver tissue stiffness is indicated by MR elastography measurements.

[12] The pharmaceutical composition according to any one of [1] to [6] above, which is for maintaining or improving a hepatic reserve function index.

[13] The pharmaceutical composition according to

[12] above, wherein the maintenance or improvement is evaluated during or at the end of drug administration compared with the state before the start of drug administration.

[14] The pharmaceutical composition according to

[12] above, wherein the maintenance or improvement is evaluated 6 to 12 months after the end of drug administration compared with the time at which drug administration ended.

[15] The pharmaceutical composition according to

[12] above, wherein the hepatic reserve function index is expressed by serum albumin concentration, serum bilirubin concentration, prothrombin activity value, or ALBI score.

[16] The pharmaceutical composition according to

[12] , wherein the hepatic reserve function index is expressed by serum bilirubin concentration, prothrombin activity value, or ALBI score.

[17] The pharmaceutical composition according to

[12] above, wherein the hepatic reserve index is expressed as a change in Child-Pugh classification (A, B, C) or a change in score.

[0012]

[18] The pharmaceutical composition according to any one of the above-mentioned [1] to [6], which is for maintaining or improving a cholestasis index.

[19] The pharmaceutical composition according to

[18] above, wherein the maintenance or improvement is evaluated 6 to 12 months after the end of drug administration compared with the time at which drug administration ended.

[20] The pharmaceutical composition according to

[18] above, wherein the cholestasis index is expressed as serum total bile acid concentration.

[21] A method for assisting in the evaluation of the therapeutic effect of 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, on a liver disease, the method comprising measuring at least one selected from liver tissue stiffness, a hepatic reserve function index, and a cholestasis index.

[22] The method described in

[21] above, wherein the measurement is performed 6 to 12 months after the end of drug administration and compared with the time at which drug administration was terminated.

[23] The method according to

[21] or

[22] above, wherein the liver tissue stiffness is indicated by fibroscan measurements.

[24] The method described in

[21] or

[22] above, wherein the hepatic reserve function index is expressed as serum albumin concentration.

[25] The method according to

[21] or

[22] above, wherein the cholestasis index is expressed as serum total bile acid concentration.

[26] 100-400mg / m 2 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human once or twice a week over 2 to 5 hours each time, and the administration is continued for 2 to 6 months.

[27] 280 mg / m 2 The method for preventing and / or treating a liver disease according to the above-mentioned

[26] , characterized in that 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human twice a week over four hours for each administration, and the administration is continued for 12 weeks.

[28] Use of 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, in the manufacture of a pharmaceutical composition for the prevention and / or treatment of liver disease, 100-400mg / m 24-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human once or twice a week over 2 to 5 hours each time, and the administration is continued for 2 to 6 months.

[29] 280 mg / m 2 The use according to the above-mentioned

[28] , characterized in that 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human twice a week over four hours each time, and the administration is continued for 12 weeks. [Effects of the Invention]

[0013] 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate or a pharmaceutically acceptable salt thereof is administered to a patient in need thereof at a dose of 100 to 400 mg / m 2 (e.g. 280mg / m 2 ) is administered intravenously once or twice a week (e.g., twice a week) over 2 to 5 hours (e.g., 4 hours) each time, and the administration is continued for 2 to 6 months (e.g., 12 weeks), thereby showing excellent therapeutic effects against liver cirrhosis (liver fibrosis). [Brief explanation of the drawings]

[0014] [Figure 1]Figure 1 shows the inhibitory effect of compounds of the present disclosure on liver fibrosis in Mdr2-KO mice. Mdr2-KO mice (MDR2KO, male, 8-10 weeks old) and FVB background control mice were administered a compound of the present disclosure (20 mg / kg, 3 times a week) for 10 weeks. Mice without treatment served as controls. A shows a scheme of the treatment protocol. B shows the results of Sirius Red staining (scale bars: 500 μm, 1 mm, and 500 μm, respectively, from the upper panel). [Figure 2] Figure 2 shows the inhibitory effect of compounds of the present disclosure on liver fibrosis in BDL mice. Wild-type C57BL / 6 mice (male, 8-10 weeks old) underwent BDL or sham surgery and were treated with compounds of the present disclosure (20 mg / kg, 3 times a week) or PBS. Animals were euthanized 14 days after surgery. Panel A shows a scheme of the treatment protocol. Panel B shows the results of hematoxylin-eosin staining, Sirius red staining, and immunohistochemical staining for CK19 (scale bars, 100 μm, 500 μm, and 250 μm, respectively, from the upper panel). [Figure 3] Figure 3 shows the inhibitory effect of compounds of the present disclosure on liver fibrosis in DDC mice. Wild-type C57BL / 6 mice (male, 8 weeks old) were fed a 0.1% DDC diet for 18 days and administered a compound of the present disclosure (20 mg / kg, 3 times a week) or PBS. Results are shown for hematoxylin-eosin staining and Sirius red staining (scale bars, 250 μm and 500 μm, respectively, from the top panel). [Figure 4] Figure 4 shows that compounds of the present disclosure reduce bile acid (BA) synthesis in Mdr2-KO mice. Mdr2-KO mice (8-10 weeks old) and FVB background control mice were administered a compound of the present disclosure (20 mg / kg, 3 times a week) for 10 weeks. Untreated mice served as controls. Liver and serum TBA, CA, and CDCA levels (n=10 per group) are shown. Results shown represent the mean ± SD of at least three independent experiments. **p<0.01; ****p<0.0001, Student's t-test. [Figure 5]Figure 5 shows that compounds of the present disclosure reduce bile acid (BA) synthesis in BDL mice. Wild-type C57BL / 6 (male, 8-10 weeks old) mice underwent BDL or sham surgery and were treated with compounds of the present disclosure (20 mg / kg, 3 times a week) or PBS. Liver TBA, CA, and CDCA levels (n = 6-9 per group) are shown. Results shown represent the mean ± SD of at least three independent experiments. *p < 0.05; **p < 0.01; ****p < 0.0001, one-way ANOVA. [Figure 6] Figure 6 shows that compounds of the present disclosure reduce bile acid (BA) synthesis in DDC mice. Wild-type C57BL / 6 (male, 8 weeks old) mice were fed a 0.1% DDC diet for 18 days and administered a compound of the present disclosure (20 mg / kg, 3 times a week) or PBS. Liver and serum TBA, CA, and CDCA levels (n=6 per group) are shown. Results shown represent the mean ± SD of at least three independent experiments. **p<0.01, unpaired Student's t-test. [Figure 7] Figure 7 shows that compounds of the present disclosure improve liver dysfunction in Mdr2-KO mice. Male Mdr2-KO mice and FVB background control mice were administered a compound of the present disclosure (20 mg / kg, 3 times per week) for 10 weeks. Untreated mice served as controls. Serum ALT, ALP, and T.Bil levels (n = 5-7 per group) are shown. Results shown represent the mean ± SD of at least three independent experiments. **p < 0.01; ***p < 0.005; ****p < 0.0001, one-way ANOVA. [Figure 8] Figure 8 shows that compounds of the present disclosure improve liver dysfunction in BDL mice. Wild-type C57BL / 6 (male, 8-10 weeks old) mice underwent BDL or sham surgery and were treated with compounds of the present disclosure (20 mg / kg, 3 times a week) or PBS. Serum ALT, ALP, and T.Bil levels (n = 6-9 per group) are shown. Results shown are representative of at least three independent experiments. Data represent mean ± SD. **p < 0.01; ***p < 0.005, one-way ANOVA. [Figure 9] Figure 9 shows that compounds of the present disclosure improve liver dysfunction in DDC mice. Wild-type C57BL / 6 (male, 8 weeks old) mice were fed a 0.1% DDC diet for 18 days and administered a compound of the present disclosure (20 mg / kg, 3 times a week) or PBS. Serum ALT, ALP, and T.Bil levels (n=6 per group) are shown. Results shown represent the mean ± SD of at least three independent experiments. **p<0.01, unpaired Student's t-test. [Figure 10] Figure 10 shows that compounds of the present disclosure improve liver fibrosis in Mdr2-KO mice. Male Mdr2-KO mice and FVB background control mice were administered a compound of the present disclosure (20 mg / kg, 3 times a week) for 10 weeks. Untreated mice served as controls. The mRNA expression levels of selected genes (Col1a1, Col1a2) in the liver as determined by RT-qPCR are shown. Results shown represent the mean ± SD of at least three independent experiments. *p<0.05; **p<0.01, one-way ANOVA. [Figure 11] Figure 11 shows that compounds of the present disclosure improve liver fibrosis in DDC mice. Wild-type C57BL / 6 (male, 8 weeks old) mice were fed a 0.1% DDC diet for 18 days and administered a compound of the present disclosure (20 mg / kg, 3 times a week) or PBS. The mRNA expression levels of selected genes (Col1a1, Col1a2, Col3a1) in the liver as determined by RT-qPCR are shown. Results shown represent the mean ± SD of at least three independent experiments. **p<0.01, unpaired Student's t-test. [Figure 12] Figure 12 is based on the results of a Phase I clinical trial of the compound of the present disclosure in patients with advanced PBC (n=5). It shows the change in serum TBA concentration before administration of the compound of the present disclosure (baseline), during administration (after 4 weeks and 8 weeks), and after 12 weeks (end of administration). Data represent the mean ± SD. Paired Student's t-test. [Figure 13]Figure 13 is based on the results of a Phase I / IIa clinical trial of a compound of the present disclosure in patients with liver cirrhosis. It shows the change in liver tissue stiffness before administration of the compound of the present disclosure (baseline) and after 12 weeks (end of administration). Paired t-test. Fibroscan was used to measure liver tissue stiffness. [Figure 14] Figure 14 is based on the results of a Phase IIa clinical trial of the compound of the present disclosure in patients with liver cirrhosis. (A) shows the changes in serum albumin concentration before administration of the compound of the present disclosure (baseline), during administration (after 3 weeks, 6 weeks, and 9 weeks), and after 12 weeks (end of administration). (B) shows the changes in serum albumin concentration before administration of the compound (baseline) and 9 months after the start of administration. [Figure 15] Figure 15 is based on the results of a clinical trial conducted on patients with liver cirrhosis using the dosing schedule of Protocol A. The figure shows the change in FIB-4 index before administration of the compound of the present disclosure (baseline) and after 12 weeks (end of administration). *p<0.05 [Figure 16] The left graph shows fibroscan measurements for each patient (KOM-6, 7, 9, 10, 12, 13, 15, 17, 22, 28, 26, 30, 32) at the start of medication (left bar), at the end of medication (12 weeks later) (center bar), and 9 months after starting medication (right bar). The right graph shows the change in liver tissue stiffness between the start of medication and 9 months after starting medication. **p<0.01; paired t-test. [Figure 17] Figure 17-1 shows the effect of the compound of the present disclosure on improving liver function. Figure 17-2 shows a case in which the condition was Child-Pugh (CP) class B. [Figure 18] Figure 18-1 shows the effect of the compound of the present disclosure on improving liver function. Figure 18-2 shows a case in which the condition was Child-Pugh (CP) class B. [Figure 19] Figure 19-1 shows the effect of the compound of the present disclosure on improving liver function. Figure 19-2 shows a case in which the condition was Child-Pugh (CP) class B. [Figure 20]20 is a graph showing the effect of improving liver fibrosis based on the results of a Phase I clinical trial of the compound of the present disclosure in hemophilia HIV / HCV co-infected liver cirrhosis patients. [Figure 21] FIG. 21 shows the effect of the compounds of the present disclosure in improving liver fibrosis. DETAILED DESCRIPTION OF THE INVENTION

[0015] In some embodiments, the present disclosure provides a pharmaceutical composition for preventing and / or treating liver disease (hereinafter also referred to as the "pharmaceutical composition of the present disclosure"), comprising 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate (foscenvivint, (also known as foscenvivint), a compound of the present disclosure, or PRI-724 or OP-724) or a pharmaceutically acceptable salt thereof as an active ingredient, wherein the pharmaceutical composition of the present disclosure is administered to a patient in need thereof at a dose of 100 to 400 mg / m 2 as foscenvivint. 2 (e.g. 280mg / m 2 ) is administered intravenously once or twice a week (e.g., twice a week) over 2 to 5 hours (e.g., 4 hours) each time, and the administration is continued for 2 to 6 months (e.g., 12 weeks), thereby showing excellent therapeutic effects against liver cirrhosis (liver fibrosis). This will be explained in detail below.

[0016] In the present disclosure, "liver disease" refers to any disease of the liver. In some embodiments, the liver disease targeted by the present invention may be any liver disease, but may also be a disease accompanied by liver fibrosis or, in some cases, a more advanced form of cirrhosis. Liver fibrosis and cirrhosis refer to a condition in which the production of fibrous tissue called extracellular matrix composed of collagen and complex carbohydrates is promoted during the process of repair of necrotic hepatocytes caused by various liver disorders, such as viral hepatitis, alcoholic liver disease, autoimmune liver disease, and metabolic liver disease, and this fibrous tissue gradually accumulates as inflammation progresses. Diseases that cause liver fibrosis and cirrhosis include, but are not limited to, viral hepatitis (e.g., hepatitis B and hepatitis C), alcoholic liver disease, autoimmune liver disease (e.g., primary biliary cholangitis), drug-induced liver injury, and metabolic liver disease (e.g., fatty liver, nonalcoholic steatohepatitis, and hemochromatosis). In some embodiments, liver diseases that are the target of prevention and treatment using the pharmaceutical compositions of the present disclosure include those accompanied by liver fibrosis or cirrhosis. Also included in some embodiments are those associated with liver fibrosis or cirrhosis due to hepatitis B or C primary biliary cholangitis, hemophilia HIV / HCV coinfection, or non-alcoholic steatohepatitis.

[0017] In the present disclosure, prevention or treatment of liver disease means, in some embodiments, improvement or maintenance of liver function.

[0018] In the present disclosure, "liver function" refers to all functions of the liver, and is not particularly limited. In some embodiments, the functions of the liver include blood storage (such as regulating circulating volume), hemoglobin processing (such as processing and excretion of hemoglobin), bile and bile pigment production and enterohepatic circulation, blood and circulatory functions such as the synthesis of plasma proteins (acute phase proteins, albumin, blood coagulation factors, steroid-binding proteins, other hormone-binding proteins, etc.) [hepatic synthetic ability], nutrient metabolism functions such as the metabolism of nutrients and vitamins (such as glucose and / or other sugars, amino acids, lipids and / or fatty acids, cholesterol, lipoproteins, fat-soluble vitamins, and water-soluble vitamins) [metabolic function], detoxification or degradation functions such as the inactivation of various substances (such as toxins, steroids such as estrogen and androsterone, and other hormones), and immune functions. In addition, hepatic mitochondria contribute to energy production in the liver through their electron transport chain [electron transport chain function] (see Sherlock's Diseases of the Liver & Biliary System, 13th ed. S. Dooley, A.S.F.Lok, G. Garcia-Tsao et al., published June 2018, Wiley-Blackwell).

[0019] In the present disclosure, "improvement and maintenance" of liver function refers to the improvement of each of the liver functions described above, the prevention or suppression (maintenance) of decline in liver function due to liver dysfunction associated with aging and disease, as well as the therapeutic effect on liver fibrosis and cirrhosis, which are causes of liver dysfunction. The effect of "improving and maintaining" liver function can also be rephrased as the therapeutic effect on liver disease. In some embodiments, "improvement and maintenance" of liver function includes, but is not limited to, improvement and maintenance of hepatic reserve capacity (liver synthetic capacity), and improvement and maintenance of bile production and enterohepatic circulation.

[0020] In some embodiments, improvement or maintenance of hepatic reserve (hepatic synthetic capacity) is evaluated by measuring the amount and function of proteins synthesized in the liver. In some embodiments, hepatic reserve can be assessed by measuring serum albumin concentration as an index of hepatic reserve. In some embodiments, serum albumin concentration can be measured by absorptiometry (e.g., the Lowry method), electrophoresis-staining densitometry, high-performance liquid chromatography-ultraviolet absorption detection, or the like. In some embodiments, hepatic reserve can also be assessed by measuring the amounts of serum alanine aminotransferase (ALT), alkaline phosphatase (ALP), cholinesterase, or cholesterol. In some embodiments, another protein synthesized in the liver is prothrombin, and a method for assessing its function is measurement of prothrombin time. Impaired liver function reduces bile secretion and inhibits the absorption of fat-soluble vitamin K. Among coagulation factors, II, VII, IX, and X are vitamin K-dependent and decrease more rapidly than other factors synthesized in the liver. Among these, factor VII has the shortest half-life, so a decline in liver synthesis acutely prolongs the prothrombin time (PT), which involves factor VII. Furthermore, although factor VII is an extrinsic coagulation factor, over time it also prolongs the activated partial thromboplastin time (ATP), which involves intrinsic coagulation factors.

[0021] In some embodiments, improvement or maintenance of bile and bile pigment production and enterohepatic circulation can be assessed by measuring serum total bile acid concentrations as an indicator of cholestasis. Bile is produced in hepatocytes and excreted through the biliary system into the duodenum. Cholestasis occurs when bile flow is blocked somewhere along this pathway. Bile components stagnate in the liver or bile ducts and even leak into the blood. Bilirubin is a yellow pigment formed by the breakdown of hemoglobin in old red blood cells. Bilirubin is transported via the bloodstream to the liver, where it is processed and then excreted in bile. Bilirubin before processing in the liver is called "indirect bilirubin," and bilirubin processed into bile is called "direct bilirubin." Together, these two are called "total bilirubin."

[0022] In some embodiments, the Child-Pugh score can be used to assess hepatic functional reserve.

[0023] The Child-Pugh score is a functional assessment method for liver cirrhosis based on five items: (1) hepatic encephalopathy, (2) ascites, (3) serum bilirubin level, (4) serum albumin level, and (5) prothrombin activity (Table 1). The total score for each item is used to assess liver cirrhosis into three levels: class A (5-6 points), class B (7-9 points), and class C (10-15 points). [Table 1]

[0024] In some embodiments, the liver disease is classified as A, B, or C according to the Child-Pugh score.

[0025] In some embodiments, the liver disease is classified by a Child-Pugh overall score of at least 5, or at least 6, or at least 7, or at least 8, or at least 9, or at least 10, or at least 11, or at least 12, or at least 13, or at least 14, or 15.

[0026] In some embodiments, hepatic functional reserve can be assessed by improvement in Child-Pugh grade (A, B, C).

[0027] In some embodiments, hepatic functional reserve can also be evaluated by the change in the Child-Pugh score (5 to 15 points) or the change in the scores (1 to 3 points) of each of the evaluation items that make up the Child-Pugh score (hepatic encephalopathy, ascites, serum bilirubin level, serum albumin level, and prothrombin activity).

[0028] In some embodiments, the ALBI grade can be used to assess hepatic functional reserve.

[0029] The ALBI grade (Albumin-bilirubin grade) is a method for evaluating liver function reserve, which is categorized into three levels based on the ALBI score calculated using only albumin and bilirubin levels. [(0.66 × log 10 Bilirubin (μmol / L) + (-0.085 × albumin (g / L)): grade 1:2:3 = ≦-2.60:>-2.60 to ≦-1.39:>-1.39.

[0030] In some embodiments, the (MELD) score can be used to assess hepatic functional reserve.

[0031] The Model for End-Stage Liver Disease (MELD) score is used to predict the short-term prognosis of patients with decompensated cirrhosis and determine liver transplant eligibility. The MELD score is calculated from three items: (1) serum bilirubin, (2) prothrombin time-international normalized ratio (PT-INR), and (3) serum creatinine level.

[0032] Serum bilirubin [Standard range] 0.3 to 1.2 (mg / dL) In the reticuloendothelial system, hemoglobin in waste red blood cells is broken down, heme is cleaved, and unconjugated (indirect) bilirubin is produced. Unconjugated bilirubin binds to albumin, is transported to the liver, and is taken up by hepatocytes from the sinusoidal side. The taken up bilirubin binds to ligandin, is transported to the endoplasmic reticulum, where it is glucuronidated by bilirubin UDP-glucuronosyl transferase (BUGT), is transported to the bile canaliculi, and is excreted from the bile canaliculi via the bile duct into the duodenum by multidrug resistance protein 2 (MRP2). Abnormalities in this bilirubin metabolism and excretion pathway result in hyperbilirubinemia. Diseases that cause elevated bilirubin are shown in Table 2. [Table 2]

[0033] Prothrombin time (PT) [Standard value] PT: 80~130(%) Prothrombin time (PT) reflects the combined clotting activity of extrinsic coagulation factors VII, X, V, and II (prothrombin) and fibrinogen. (PT) is the actual measured value (seconds). It is the % activity relative to normal plasma. PT is a more sensitive indicator of hepatic reserve (protein synthesis ability) than albumin, and will be lower in severe liver damage, vitamin K deficiency, and warfarin administration.

[0034] In some embodiments, the therapeutic effect on liver fibrosis or cirrhosis can be evaluated by observing the state of fibrosis and defibrosis in the liver parenchyma. In some embodiments, histopathological staining (e.g., Sirius Red staining) is used. Sirius Red staining is used to evaluate fibrosis and stains collagen fibers red. In some embodiments, evaluation can also be performed by measuring liver tissue stiffness. In some embodiments, the improvement or maintenance of liver tissue stiffness can be evaluated using measurements obtained by, for example, a fibroscan test. A fibroscan test involves placing a special "probe" on the surface of the body and measuring the liver stiffness and fat content in liver tissue based on the vibrations and ultrasound propagation patterns emitted from the probe. The basic principle of MR elastography (MRE) is to convert the vibration phase of shear waves generated in the liver by an external vibration device into the rotational phase of protons, and this phase difference is detected in an MRI phase image to obtain the shear modulus. The velocity (V) of elastic waves propagating in the liver is calculated using the shear modulus (μ) and density (ρ) of the material. 2 =μ / ρ.

[0035] In some embodiments, the therapeutic effect can also be confirmed by assessing liver fibrosis by measuring the expression level of collagen genes.

[0036] In some embodiments, the FIB-4 index can be measured to assess the progression of liver fibrosis.

[0037] The FIB-4 index is a scoring system that combines blood test data to evaluate the progression of liver fibrosis. This test method calculates a score by combining four blood test items: AST value, ALT value, platelet count, and age, and the degree of progression of fibrosis is evaluated from the resulting value. It is a score that predicts liver fibrosis in hepatitis C. Recently, it has been adapted for other liver diseases such as NASH. Using the FIB-4 index as an indicator in patients with fatty liver, early detection of cases of progression of liver fibrosis is considered important in the follow-up of NAFLD patients.

[0038] In some embodiments, APRI can be measured to assess the progression of liver fibrosis.

[0039] APRI (aspartate aminotransferase to platelet ratio index) evaluates the degree of fibrosis by combining AST, ALT, and platelet count. It is a score that predicts liver fibrosis in hepatitis C patients.

[0040] In some embodiments, the effect of "improving or maintaining" liver function, i.e., the "therapeutic effect on liver disease," can be evaluated based on the above-mentioned indices. In some embodiments, the above-mentioned indices can be used as an aid in evaluating the effect. In some embodiments, measuring each indices can determine the optimal dosage for treatment. In some embodiments, at least one, two, or all three of liver tissue stiffness (e.g., fibroscan measurement value), hepatic reserve function index (e.g., serum albumin concentration), and cholestasis index (e.g., serum total bile acid concentration) can be used as evaluation indices.

[0041] The above evaluation indexes are usually measured before starting drug administration, during drug administration, and at the end of drug administration, and can be used to evaluate the drug's effect of improving and maintaining liver function (therapeutic effect on liver disease). Furthermore, by measuring the indexes a certain period (e.g., 6 to 12 months) after the end of drug administration, the sustainability of the drug's effect of further improving and maintaining liver function (therapeutic effect on liver disease) can be evaluated.

[0042] In some embodiments, the pharmaceutical composition of the present disclosure comprises 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof. In some embodiments, the pharmaceutical composition of the present disclosure comprises 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, as an active ingredient.

[0043] In this disclosure, "pharmaceutically acceptable" means useful in the preparation of pharmaceutical compositions that are generally safe, non-toxic, and not biologically or otherwise undesirable, and includes acceptable for veterinary as well as human pharmaceutical use.

[0044] In the present disclosure, "pharmaceutically acceptable salts" refers to salts of the compounds of the present invention that are pharmaceutically acceptable, as defined above, and that possess the desired pharmacological activity. In some embodiments, such salts include salts of inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and phosphoric acid; or salts of acetic acid, propionic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, o-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, benzoic ... Examples of suitable pharmaceutically acceptable salts include acid addition salts formed with organic acids such as sulfonic acid, p-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo[2.2.2]oct-2-ene-1-carboxylic acid, glucoheptonic acid, 4,4'-methylenebis(3-hydroxy-2-ene-1-carboxylic acid), 3-phenylpropionic acid, trimethylacetic acid, tert-butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, and muconic acid. In some embodiments, pharmaceutically acceptable salts also include base addition salts, which may be formed when acidic protons present are capable of reacting with inorganic or organic bases. In some embodiments, acceptable inorganic bases include sodium hydroxide, sodium carbonate, potassium hydroxide, aluminum hydroxide, and calcium hydroxide. In some embodiments, acceptable organic bases include ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine, and the like.

[0045] In some embodiments, the pharmaceutical compositions of the present disclosure may be in a dosage form for oral use or a dosage form for parenteral use. These dosage forms can be formulated by those skilled in the art by appropriately combining pharmaceutically acceptable carriers and additives and blending them into a unit dosage form required for generally accepted pharmaceutical practice. In some embodiments, the pharmaceutical compositions of the present disclosure can be manufactured according to known methods, such as those described in the Japanese Pharmacopoeia or the United States Pharmacopoeia (USP). In some embodiments, methods of administration of the pharmaceutical compositions of the present disclosure include intravenous administration, continuous intravenous administration, and the like.

[0046] In some embodiments, the pharmaceutical composition of the present disclosure is administered to humans as a pharmaceutical preparation (e.g., injection, infusion) formulated by a conventional method. In some embodiments, the administration is in the range of 100 to 400 mg / m2 in terms of the amount of the active ingredient. 2 The dosage is:

[0047] In some embodiments, the administration is in the range of 200 to 300 mg / m2 in terms of the amount of active ingredient. 2 The dosage is:

[0048] In some embodiments, the dose is equivalent to 200 mg / m of the active ingredient. 2 , 210 mg / m 2 , 220 mg / m 2 , 230 mg / m 2 , 240 mg / m 2 , 250 mg / m 2 , 260 mg / m 2 , 270 mg / m 2 , 280 mg / m 2 , 290 mg / m 2 , 300 mg / m 2 is administered at a dose of

[0049] In some embodiments, the dose is equivalent to 280 mg / m of active ingredient. 2 The dosage is:

[0050] In some embodiments, the dose is administered intravenously over at least one hour, at least once a week.

[0051] In some embodiments, the dose is administered intravenously once or twice weekly over 2-5 hours each time, hi some embodiments, the dose is administered intravenously twice weekly over 4 hours each time.

[0052] In some embodiments, the administration is continued for one month.

[0053] In some embodiments, the administration is continued for 2 to 6 months, hi some embodiments, the administration is continued for 12 weeks.

[0054] In some embodiments, the pharmaceutical composition of the present disclosure is administered to a human as a conventionally formulated pharmaceutical preparation (e.g., injection, infusion) intravenously once or twice a week over 2 to 5 hours each time, with the administration continuing for 2 to 6 months. In some embodiments, the pharmaceutical composition of the present disclosure is administered to a human as a conventionally formulated pharmaceutical preparation (e.g., injection, infusion) intravenously twice a week over 4 hours each time, with the administration continuing for 12 weeks.

[0055] The present invention will be described in more detail below with reference to examples, but these examples are not intended to limit the scope of the present invention. [Example]

[0056] All experiments were conducted in accordance with the National Academy of Sciences' Guide for the Care and Use of Laboratory Animals. The study protocol was approved by the Tokyo Metropolitan Komagome Hospital Research Committee. All analyses using human samples were approved by the Tokyo Metropolitan Komagome Hospital Ethics Committee. This study adhered to the principles of the Declaration of Helsinki. All experimental animals (mice) were maintained in ventilated cages under a 12-h / 12-h light / dark cycle with free access to enrichment, water, and food.

[0057] (List of abbreviations) ALP: alkaline phosphatase ALT: alanine aminotransferase BA: bile acid BDL: bile duct ligation CA: cholic acid CDCA: chenodeoxycholic acid CK19: cytokeratin-19 FXR: farnesoid X receptor MDR2: multidrug resistance-associated protein 2 PBC: primary biliary cholangitis PSC: primary sclerosing cholangitis T.Bil: total bilirubin TBA: total bile acid

[0058] Materials and Methods 1. Mdr2-KO Mouse Model Mdr2-KO (FVB.129P2-Abcb4tm1Bor / J, #002539) mice were purchased from Jackson Laboratory (Bar Harbor, ME, USA), and wild-type littermates on an FVB / NJ background served as controls. Male Mdr2-KO mice (8–10 weeks old) and their littermate controls were intraperitoneally injected with 20 mg / kg of a compound of the present disclosure (foscenvivint; Prism BioLab, Tokyo, Japan) dissolved in PBS or PBS as a control, three times a week for 10 weeks.

[0059] 2. BDL Mouse Model Eight to ten week old male wild-type (C57BL / 6J) mice were obtained from Japan SLC (Shizuoka, Japan). The common bile duct above the pancreas was incised and BDL was performed as previously reported (Osawa Y, et al. Inhibition of Cyclic Adenosine Monophosphate (cAMP)-response Element-binding Protein (CREB)-binding Protein (CBP) / beta-Catenin Reduces Liver Fibrosis in Mice. eBioMedicine 2, 1751-1758 (2015).) The mice were intraperitoneally administered 20 mg / kg of a compound of the present disclosure dissolved in PBS three times a week.

[0060] 3. DDC Mouse Model Eight-week-old C57BL / 6J wild-type male mice were fed a 0.1% DDC enriched diet (Sigma-Aldrich, St. Louis, MO, USA) for 18 days.

[0061] 4. Bilirubin Serum bilirubin was measured using the QuantiChrom Bilirubin Assay Kit (BioAssay Systems, Hayward, CA, USA).

[0062] 5.BA analysis Serum and liver TBA, CA, and CDCA concentrations were analyzed using the Total Bile Acid Assay Kit, Cholic Acid ELISA Kit, and Chenodeoxycholic Acid ELISA Kit (Cell Biolabs, San Diego, CA, USA), respectively, according to the manufacturer's instructions.

[0063] 6. RT-qPCR RNA extraction, DNA removal, and reverse transcription from liver tissue and cultured cells were performed using RNeasy and DNase Kits (Qiagen, Valencia, CA, USA) and the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Foster City, CA, USA). qPCR was performed in triplicate on a LightCycler 480 (Roche Applied Science, Mannheim, Germany) using probe and primer sets purchased from Thermo Fisher Scientific and TaqPath qPCR Master Mix, CG (Applied Biosystems). Target gene expression levels were normalized to GAPDH expression levels in each sample. (Mouse primer set)

[0064] [Table 3]

[0065] 7.Histological analysis Mouse liver tissue was fixed in 10% formalin, sectioned, and stained with hematoxylin and eosin (HE). Collagen deposits were stained with Sirius Red (saturated picric acid plus 0.1% Direct Red 80 and 0.1% Fast Green FCF). Additionally, samples were immunohistochemically stained using an antibody against cytokeratin 19 (Abcam, Cambridge, UK). Sirius Red-positive areas were quantified using HistoQuant software (3DHISTECH, Budapest, Hungary). (Hematoxylin and eosin (HE) staining) HE staining is a staining method that allows for the differentiation of cell nuclei and cytoplasm, enabling the observation of tissue morphology. HE staining allows for an overall understanding of cell and tissue structure. Sections are cut from paraffin blocks of liver tissue pre-fixed with Bouin's solution and stained with Lillie-Mayer's Hematoxylin (Muto Chemicals, Japan) and eosin solution (Fujifilm Wako Pure Chemical Industries, Japan). (Sirius Red dye) To visualize collagen deposition, Bouin-fixed liver sections were stained with picrosirius red solution (Waldeck GmbH & Co., Germany). For quantitative analysis, Sirius red-stained sections near the central vein were captured at 200x magnification using a digital camera (DFC280, Leica, Germany). The positive areas were measured in five fields per section using ImageJ software (ImageJ, National Institutes of Health, USA).

[0066] 8. Fib-4 index measurement The Fib-4 Index is a score used to predict liver fibrosis. It is calculated by combining four items: AST, ALT, platelet count, and age. The resulting value can be used to evaluate the degree of progression of fibrosis.

[0067]

number

[0068] 9. Fibroscan Test Measurement using FibroScan, a non-invasive testing method based on transient elastography, which measures the propagation speed of pulsed vibration waves within tissue in terms of elasticity (kPa) using ultrasound image analysis. FibroScan manufactured by ECHOSENS is used.

[0069] 10. Serum albumin concentration Serum albumin is a protein produced in the liver, and its amount is known to decrease as liver function declines. Serum albumin can be measured by standard methods. For example, the amount of albumin in a sample can be determined by using a reagent that binds to albumin to produce a pigment, and measuring the pigment spectrophotometrically. One such pigment is bromocresol green, which reacts with albumin at around pH 4.0 to produce a blue albumin-binding pigment. A commercially available measurement reagent (Shikaliquid ALB, Kanto Chemical Co., Ltd.) can also be used. The reagent is mixed with the sample, and the absorbance of the resulting bound dye is measured.

[0070] Example 1 Preclinical study (evaluation in PBC model mice) 1 (improvement of liver fibrosis) As non-clinical trial models of primary biliary cholangitis (PBC), bile duct ligation model mice (BDL mice), MDR2 knockout mice (Mdr2-KO mice), and bile duct disorder model mice (DDC mice) were used to investigate the liver fibrosis-improving effect of the compounds of the present disclosure. MDR2KO mice and BDL mice were treated with the compounds of the present disclosure according to the protocols shown in Figures 1A and 2A, respectively. DDC mice were wild-type C57BL / 6 male mice, 8 weeks old, fed a 0.1% DCC diet for 18 days. During this time, the compounds of the present disclosure (20 mg / kg, three times per week) or PBS were intraperitoneally administered. After treatment, livers were harvested, and the anti-fibrotic effects of the compounds of the present disclosure were examined by Sirius Red staining of liver tissue. Sirius Red-positive areas indicate collagen deposition. Hematoxylin-eosin staining was also performed on BDL and DDC mice. In both model mice, a significant decrease in the Sirius Red-positive area, i.e., a decrease in the fibrotic area, was observed (Figures 1 to 3), confirming the anti-fibrotic effects of the compounds of the present disclosure.

[0071] Example 2 Preclinical study (evaluation in PBC model mice) 2 (cholestasis improvement effect) As in Example 1, BDL mice, Mdr2-KO mice, and DDC mice were used as PBC model mice to examine the cholestasis-ameliorating effects of compounds of the present disclosure. Because bile acid (BA) metabolism is involved in hepatic fibrosis due to cholestasis, BA levels (total bile acids (TBA), cholic acid (CA), and chenodeoxycholic acid (CDCA)) were measured. The results are shown in Figure 4 (Mdr2-KO mice), Figure 5 (BDL mice), and Figure 6 (DDC mice). In Mdr2-KO mice, liver TBA and CA levels were unaffected by the compounds of the present disclosure, but CDCA levels were reduced. Serum TBA, CA, and CDCA levels were reduced by the compounds of the present disclosure (Figure 4). Similarly, the compounds of the present disclosure reduced liver TBA, CA, and CDCA levels in BDL mice (Figure 5) and in DDC mice (Figure 6).

[0072] Example 3 Preclinical study (evaluation in PBC model mice) 3 (liver function improvement effect) As in Example 1, the liver function-improving effects of compounds of the present disclosure were investigated using BDL mice, Mdr2-KO mice, and DDC mice as PBC model mice. Serum alanine aminotransferase (ALT) is an enzyme produced in hepatocytes and released into the blood upon hepatocyte destruction, resulting in elevated serum levels. Alkaline phosphatase (ALP) is an enzyme that breaks down phosphate compounds and is produced in the liver, kidneys, intestinal mucosa, and bones. It is processed in the liver and released into bile. When bile flow is impaired (cholestasis) due to bile duct obstruction caused by gallstones, cholangitis, or biliary tract cancer, or when liver function is impaired, ALP in bile refluxes and flows into the blood. Therefore, ALP levels are significantly elevated in cholestasis. Bilirubin is divided into indirect bilirubin, which is processed by the liver, and direct bilirubin, which is processed and enters bile (together referred to as total bilirubin). Direct bilirubin is excreted from the bile duct. When liver function is impaired, the liver is unable to process indirect bilirubin, resulting in large amounts remaining in the blood.On the other hand, when biliary system damage results in insufficient bile excretion, direct bilirubin increases in the blood. In this example, the serum levels of ALT, ALP, and total bilirubin were measured for each PBC model mouse. The results are shown in Figure 7 (Mdr2-KO mice), Figure 8 (BDL mice), and Figure 9 (DDC mice). In all PBC model mice, liver damage was alleviated, as indicated by decreased ALT, ALP, and T.Bil levels.

[0073] Example 4 Preclinical study (evaluation in PBC model mice) 4 (improvement of collagen gene expression) Mdr2-KO mice and DDC mice were used as PBC model mice to examine the effect of the compounds of the present disclosure on improving collagen gene expression levels. Collagen, particularly type IV collagen, is known as a marker of liver fibrosis. Type IV collagen constitutes the basement membrane. Although basement membranes are not present in normal liver sinusoids, basement membrane proliferation occurs as liver fibrosis progresses, resulting in increased expression of type IV collagen. In this example, the expression level of collagen genes in hepatocytes was measured for each PBC mouse model. The results are shown in Figure 10 (Mdr2-KO mice) and Figure 11 (DDC mice). In both PBC mouse models, reduced liver fibrosis was confirmed, as indicated by a decrease in collagen gene expression.

[0074] Example 5 Clinical trial (evaluation in PBC patients) (improvement of cholestasis) This example is based on the results of a Phase I study designed to investigate the safety and tolerability of compounds of the present disclosure in patients with PBC and to determine recommended doses. The subjects were patients diagnosed with primary biliary cholangitis, and as a result of liver tissue examination, were diagnosed with advanced fibrosis (Scheuer stage III or higher). The dosing schedule was as follows: the compound of the present disclosure was intravenously administered twice a week (4 hours) for 12 weeks. However, 7 days before the first cycle administration, the dose scheduled for the first cycle was administered once by continuous intravenous administration over 4 hours, and safety and pharmacokinetics were evaluated from the day of administration to the day after administration. The dose level was two doses (280 mg / m 2 / 4 hours, 380mg / m 2 / 4 hours). After completing the 12-week dosing schedule of compounds of the present disclosure, serum total bile acid concentrations (TBA concentrations) were measured, and the results are shown in Figure 12. A clear decrease in TBA concentration was observed after drug treatment, confirming the cholestasis-ameliorating effect of the compound of the present disclosure.

[0075] Example 6 (Evaluation in Hepatitis Patients) (Effect of Improving Liver Tissue Hardness) This example is based on the results of a Phase I study designed to evaluate the safety and pharmacokinetics of compounds of the present disclosure when administered to patients with HCV or HBV cirrhosis and to determine recommended doses of compounds of the present disclosure, and a Phase II study designed to evaluate the efficacy and safety of recommended doses of compounds of the present disclosure administered to patients with HCV or HBV cirrhosis. The dosing schedule in the Phase I study was (Level 1) 140 mg / m 2 / 4 hours, (Level 2) 280 mg / m2 / 4 hours, (Level 3) 380 mg / m 2 The study consisted of three doses administered over 4 consecutive hours, twice weekly, over a 4-hour intravenous infusion (administration time tolerance: ±15 minutes). This was repeated as a single dose for 12 cycles (12 weeks in total). The single dose was administered 7 days before the first cycle, at the dose scheduled for the first cycle, over a 4-hour intravenous infusion (administration time tolerance: ±15 minutes). Safety and pharmacokinetics were evaluated from the day of administration to the day after administration. In the Phase II (IIa) study, the recommended dose (Level 2) determined in the Phase I study was administered intravenously over 4 hours twice a week for 12 cycles (12 weeks in total) (Protocol A). In a Phase I study, liver tissue stiffness was measured using FibroScan after a 12-week dosing schedule of compounds of the present disclosure, and the results are shown in Figure 13. The drug treatment resulted in a clear decrease in liver tissue stiffness, confirming the liver tissue stiffness-improving effect of the compound of the present disclosure. In particular, good results were obtained with the drug treatment at Level 2. In a Phase II study, serum albumin levels were measured using the dosing schedule of Protocol A. The results are shown in Figure 14A. Administration of a compound of the present disclosure was confirmed to have an improving effect on serum albumin levels. Following completion of the dosing schedule of a compound of the present disclosure using Protocol A, serum albumin levels were measured. The results are shown in Figure 14B. It was confirmed that the improving effect on serum albumin levels persisted even 9 months after the start of dosing with a compound of the present disclosure. In the phase II study, the FIB-4 index was examined after the completion of the dosing schedule of Protocol A. The results are shown in Figure 15. A significant tendency toward a decrease was observed. Liver tissue stiffness was measured using FibroScan after completion of the dosing schedule of the compound of the present disclosure in Protocol A. The results are shown in Figure 16. It was confirmed that the improvement effect on liver tissue stiffness continued even 9 months after the start of dosing with the compound of the present disclosure. In a Phase II study, ALBI scores were examined 6 months after the completion of the Protocol A dosing schedule. The results are shown in Figure 17-1. Figure 17-2 shows a case with a Child-Pugh (CP) classification B condition. Six months after the completion of administration of the compound of the present disclosure, improvement in ALBI scores suggested improvement in liver function. In a Phase II study, serum albumin levels were examined 6 months after the completion of the Protocol A dosing schedule. The results are shown in Figure 18-1. Figure 18-2 shows a case with a Child-Pugh (CP) classification B condition. This included a case in which an albumin preparation was used during administration of the compound of the present disclosure (KOM-009), a case in which ascites paracentesis was performed 6 months after the completion of administration of the compound of the present disclosure (KOM-021), and a case in which an albumin preparation was used within 28 days of the completion of administration of the compound of the present disclosure due to moderate or greater amounts of ascites (KOM-033). Excluding three cases in which the evaluation of liver function was affected and two cases (KOM-012, KOM-018) in which results were not obtained 6 months after the end of administration of the compound of the present disclosure, two of the four cases in CP classification B showed an improvement in CP score (serum albumin level rating) from 2 points (2.8-3.5 g / dL) to 1 point (over 3.5 g / dL) 6 months after the end of administration. Six months after the end of administration of the compound of the present disclosure, improvement in liver function due to improvement in serum albumin levels was suggested. In a Phase II study, prothrombin time activity was measured 6 months after the completion of the Protocol A dosing schedule. The results are shown in Figure 19-1. Figure 19-2 shows cases with Child-Pugh (CP) classification B disease. This included a case in which albumin preparations were used during administration of the compound of the present disclosure (KOM-009), a case in which ascites paracentesis was performed 6 months after the completion of administration of the compound of the present disclosure (KOM-021), and a case in which albumin preparations were used by 28 days after the completion of administration of the compound of the present disclosure (KOM-033) due to moderate or severe ascites. Excluding three cases in which liver function assessment was affected and two cases in which no results were obtained 6 months after the completion of administration of the compound of the present disclosure (KOM-012 and KOM-018), three of the four CP classification B cases showed an improvement in their CP score (prothrombin time activity score) from 2 points (40-70%) to 1 point (>70%) 6 months after the completion of administration. Six months after the end of administration of the compound of the present disclosure, improvement in prothrombin time activity values suggested improvement in liver function.

[0076] Example 7 (Evaluation in patients with hemophilia and cirrhosis due to HIV / HCV coinfection) This example is based on the results of a Phase I study aimed at investigating the safety and tolerability of administering the compounds of the present disclosure to patients with cirrhosis due to hemophilia HIV / HCV coinfection. The two dosing schedules were 140 mg / m² / 4 hours (Level 1) and 280 mg / m² / 4 hours (Level 2), administered twice weekly over 4 consecutive hours via intravenous infusion (administration time tolerance: ±15 minutes). This was administered as a single dose for 12 cycles (total of 12 weeks). The single dose was administered 14 days before the first cycle, at the dose scheduled for that cycle, administered intravenously over 4 consecutive hours (administration time tolerance: ±15 minutes). Safety and pharmacokinetics were evaluated from the day of administration to the day after administration. After the 12-week dosing schedule of the compound of the present disclosure was completed, liver tissue stiffness was measured using FibroScan, and the FIB-4 index and APRI were calculated. The results are shown in Figures 20, 21A, and 21B, respectively. The liver tissue stiffness measured by FibroScan showed a decrease from baseline in both the FIB-4 index and APRI at levels 1 and 2, with the liver tissue stiffness measured by FibroScan and APRI showing a greater decrease at level 2. After administration of the compound of the present disclosure, a decrease in liver stiffness measured by FibroScan, and a tendency toward a decrease in the FIB-4 index and APRI score were confirmed.

[0077] Example 8 (Evaluation in patients with decompensated liver cirrhosis) This example is based on the design of a Phase II study aimed at evaluating the efficacy, safety, and pharmacokinetics of administering a compound of the present disclosure to patients with decompensated cirrhosis caused by HCV or HBV infection and patients with decompensated cirrhosis caused by non-alcoholic steatohepatitis (including suspected). The severity of decompensated cirrhosis is Child-Pugh classification B. Patients with decompensated cirrhosis caused by HCV or HBV infection are divided into Cohort A, and patients with decompensated cirrhosis caused by non-alcoholic steatohepatitis (including suspected) are divided into Cohort B, and the compound or placebo is administered to these patients under double-blind conditions. The administration schedule is a 280 mg / m2 dose administered intravenously over 3-4 consecutive hours (administration time tolerance: ±15 minutes). Cohort A will be randomly assigned to three groups (one receiving the compound twice a week, one receiving the compound and a placebo once a week, and one receiving a placebo twice a week), while Cohort B will be randomly assigned to two groups (one receiving the compound twice a week and one receiving a placebo twice a week). Patients will be administered the compound for 24 weeks and observed for 52 weeks after the start of administration. Efficacy evaluation items will include hepatic reserve index (Child-Pugh score, ALBI score, MELD score, Child-Pugh classification, mALBI grade, serum albumin level, serum bilirubin level, prothrombin activity level), liver fibrosis index (Fibroscan liver tissue stiffness, MRE liver tissue stiffness, serum fibrosis marker, FIB-4 index), dosage and frequency of albumin preparations used in the treatment of ascites, events associated with decompensated liver cirrhosis (esophageal and gastric variceal bleeding, ascites, etc.), and severity of ascites and hepatic encephalopathy. [Industrial Applicability]

[0078] 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate at 100 to 400 mg / m 2 It is suggested that when administered intravenously to humans at a dose of 100 mg once or twice a week over 2 to 5 hours each time, and the administration is continued for 2 to 6 months, it shows an excellent therapeutic effect against liver cirrhosis (liver fibrosis). Therefore, it is suggested that a pharmaceutical composition containing the compound is effective in preventing and / or treating liver diseases.

Claims

1. 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human twice a week over four hours for 12 weeks, characterized in that 280 mg / m2 of 4-({(6S,9S,9aS)-1-(benzylcarbamoyl)-2,9-dimethyl-4,7-dioxo-8-[(quinolin-8-yl)methyl]octahydro-2H-pyrazino[2,1-c][1,2,4]triazin-6-yl}methyl)phenyl dihydrogen phosphate, or a pharmaceutically acceptable salt thereof, is administered intravenously to a human twice a week over four hours for each administration, and the administration is continued for 12 weeks. A pharmaceutical composition for preventing and / or treating liver disease, comprising phosphate, or a pharmaceutically acceptable salt thereof, the liver disease is accompanied by liver fibrosis or liver cirrhosis with advanced liver fibrosis, the pharmaceutical composition is for maintaining or improving an evaluation index of liver disease selected from liver tissue stiffness, a hepatic reserve function index, and a cholestasis index; The evaluation index of liver disease is maintained or improved during or at the end of drug administration compared to before the start of drug administration, Furthermore, the evaluation index of the liver disease is maintained or improved 6 to 12 months after the end of drug administration compared to the time when the drug administration was completed, Pharmaceutical compositions.

2. 2. The pharmaceutical composition according to claim 1, wherein the liver fibrosis or liver cirrhosis resulting from advanced liver fibrosis is a disease caused by hepatitis B or C or primary biliary cholangitis (PBC).

3. 2. The pharmaceutical composition according to claim 1, wherein the liver fibrosis or liver cirrhosis resulting from advanced liver fibrosis is a disease caused by hemophilia, HIV / HCV coinfection, or non-alcoholic steatohepatitis.

4. 2. The pharmaceutical composition according to claim 1, wherein the liver disease is classified as A, B, or C according to the Child-Pugh score.

5. The pharmaceutical composition according to claim 1, wherein the liver tissue stiffness is indicated by fibroscan measurement value.

6. The pharmaceutical composition according to claim 1, wherein liver tissue stiffness is indicated by MR elastography measurements.

7. The pharmaceutical composition according to claim 1, wherein the hepatic reserve function index is expressed as serum albumin concentration.

8. The pharmaceutical composition according to claim 1, wherein the hepatic reserve function index is expressed by serum bilirubin concentration, prothrombin activity, or ALBI score.

9. 2. The pharmaceutical composition according to claim 1, wherein the hepatic functional reserve index is expressed as a change in Child-Pugh classification (A, B, C) or a change in score.

10. The pharmaceutical composition according to claim 1, wherein the hepatic reserve function index is expressed by the MELD score.

11. The pharmaceutical composition according to claim 1, wherein the cholestasis index is expressed as serum total bile acid concentration.

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