Saroglitazar Magnesium for Treatment of Primary Biliary Cholangitis

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Primary Biliary Cholangitis

In brief

Saroglitazar Magnesium 1 mg and 2 mg tablets for treatment of subjects with Primary Biliary Cholangitis (PBC)

Key facts

Study ID

NCT05133336

Run by

Zydus Therapeutics Inc.

People needed

196

Starts

2022-04-01

Expected to finish

2025-05-07

Last updated by the study team

2026-04-30

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males or females, between 18 and 75 years of age, both inclusive at screening.
• Subjects on ursodeoxycholic acid (UDCA) for at least 12 months at a therapeutic dose (at least 13 mg/kg per day) and a stable dose for 6 months prior to Screening Visit and having ALP ≥ 1.67 x ULN.
• OR Subjects who are unable to tolerate UDCA and did not receive UDCA for at least 3 months prior to the date of screening and having ALP ≥ 1.67 x ULN.
• History of confirmed PBC diagnosis, based on American Association for the Study of Liver Disease [AASLD] and European Association for Study of the Liver [EASL] Practice Guidelines, as demonstrated by the presence of at least ≥ 2 of the following 3 diagnostic factors:
• History of elevated ALP levels for at least 6 months prior to screening
• Positive anti-mitochondrial antibodies (AMA) titer OR positive PBC specific antibodies (anti-GP210 and/or anti-SP100 and/or antibodies against the major M2 components [PDC-E2, 2-oxo-glutaric acid dehydrogenase complex]) if AMA is negative
• Liver biopsy consistent with PBC
• ALP ≥ 1.67 x ULN at both Visits 1 and 2 and < 30% variance between the levels from Visit 1 to Visit 2
• Total bilirubin < 2 x ULN at screening (Visit 1)
• Must provide written informed consent and agree to comply with the trial protocol.

You may not qualify if…

• Consumption of 2 standard alcohol drinks per day if male and 1 standard alcohol drink per day if female for at least 3 consecutive months (12 consecutive weeks) within 5 year before screening (Note: 1 unit = 12 ounces of beer, 4 ounces of wine or 1 ounce of spirits/hard liquor).
• History or presence of other concomitant liver diseases at screening:
• Chronic hepatitis B or C virus (HBV, HCV) infection. (Note: However, If the subject has been treated for the HCV infection and has been cured for a duration of more than 2 years from screening, such subjects can be enrolled in the study)
• Primary sclerosing cholangitis (PSC).
• Alcoholic liver disease.
• Autoimmune hepatitis (AIH) indicative of PBC with overlap syndrome.
• Note: The Paris criteria are commonly used to define the presence of PBC with features of AIH and have been endorsed by EASL and AASLD. According to these criteria, a diagnosis can be made in a patient with PBC as follows:
• At least two of the following:
• I. ALP > 2 x ULN or GGT > 5 x ULN. II. AMA positive III. Florid bile duct lesion on histology. AND
• At least two of the following three features:
• I. ALT > 5 x ULN. II. Immunoglobulin G serum levels > 2 x ULN or smooth muscle autoantibody positive.
• III. Moderate to severe interface hepatitis on histology. e. Hemochromatosis. f. Non-alcoholic steatohepatitis (NASH) on historical biopsy. 3.Cirrhosis with complications, including history or presence of: spontaneous bacterial peritonitis, hepatocellular carcinoma, ascites requiring treatment, encephalopathy, known large esophageal varices or history of variceal bleeding within one year prior to screening or history of hepatorenal syndrome.
• Medical conditions that may cause non-hepatic increases in ALP (e.g., Paget's disease) or which may diminish life expectancy to < 2 years, including known cancers.
• Use of thiazolidinediones or fibrates (within 12 weeks prior to screening). 7.Use of obeticholic acid (OCA), azathioprine, cyclosporine, methotrexate, mycophenolate, pentoxifylline, budesonide and other systemic corticosteroids (Note: Prednisone dose should not be more than 10 mg per day); potentially hepatotoxic drugs (including α-methyl-dopa, sodium valproic acid, isoniazid, or nitrofurantoin) (within 12 weeks prior to screening).
• History of bowel surgery (gastrointestinal [bariatric] surgery in the preceding 1 year or undergoing evaluation for gastrointestinal surgery (bariatric surgery for obesity, extensive small-bowel resection) or orthotopic liver transplant (OLT) or listed for OLT.
• Type 1 diabetes mellitus. 11.Unstable cardiovascular disease, including:
• a. Unstable angina, (i.e., new or worsening symptoms of coronary heart disease in the 12 weeks before screening and throughout the Screening Period), acute coronary syndrome in the 24 weeks before screening and throughout the Screening Period, acute myocardial infarction in the 12 weeks before screening and throughout the Screening Period or heart failure of New York Heart Association class (III - IV) or worsening congestive heart failure, or coronary artery intervention, in the 24 weeks before screening and throughout the Screening Period.
• b. History/current unstable cardiac dysrhythmias. c. Uncontrolled hypertension at screening. d. Stroke or transient ischemic attack in the 24 weeks before screening. 12.History of intracranial hemorrhage, arteriovenous malformation, bleeding disorder, coagulation disorders, or screening blood tests that, in the opinion of the Investigator, indicate altered coagulability (e.g., PT, INR, aPTT) at screening.
• An uncontrolled thyroid disorder
• Uncontrolled hyperthyroidism: defined as any history of hyperthyroidism that has either not been treated with either radioactive iodine and/or surgery or that has been treated with radioactive iodine and/or surgery, but has required ongoing continuous or intermittent use of thyroid hormone synthesis inhibitors (i.e., methimazole or propylthiouracil) in the 24 weeks before screening.
• Uncontrolled hypothyroidism: defined as initiation of thyroid hormone replacement therapy or dose adjustment of replacement therapy in the 12 weeks before screening.
• History of myopathies or evidence of active muscle disease demonstrated by CPK ≥ 5 x ULN at screening.
• Subjects whose ALT, AST, or ALP exceeds by more than 50% on Visit 2 reading compared to Visit 1. Note: If the ALT, AST, or ALP values on Visit 2 exceed by more than 50% from Visit 1, then a third value will be measured (within 1- 2 weeks) to assess for the trend. If the third value shows continued increase ≥ 10%, then subject is considered ineligible for randomization.
• Any of the following laboratory values at screening:
• a. Platelets < 50 × 109/L b. Albumin < 2.8 g/dL c. eGFR < 45 mL/min/1.73 m2 d. ALP > 10 x ULN e. ALT or AST > 250 U/L 17.Participation in another interventional clinical study and receipt of any other investigational medication (within 12 weeks prior to randomization up to end of study).

Where it is running

• Zydus US021 — Tucson, Arizona, United States
• Zydus US013 — Los Angeles, California, United States
• Zydus US011 — Pasadena, California, United States
• Zydus US043 — Sacramento, California, United States
• Zydus US022 — Aurora, Colorado, United States
• Zydus US037 — New Haven, Connecticut, United States
• Zydus US027 — Jacksonville, Florida, United States
• Zydus US006 — Lakewood Rch, Florida, United States
• Zydus US005 — Miami, Florida, United States
• Zydus US028 — Sarasota, Florida, United States
• Zydus US019 — Tampa, Florida, United States
• Zydus US020 — Marietta, Georgia, United States
• Zydus US001 — Indianapolis, Indiana, United States
• Zydus US034 — Iowa City, Iowa, United States
• Zydus US036 — Marrero, Louisiana, United States
• Zydus US023 — Rochester, Minnesota, United States
• Zydus US030 — St Louis, Missouri, United States
• Zydus US024 — Omaha, Nebraska, United States
• Zydus US038 — Manhasset, New York, United States
• Zydus US035 — Rochester, New York, United States
• Zydus US002 — Charlotte, North Carolina, United States
• Zydus US014 — Cincinnati, Ohio, United States
• Zydus US015 — Philadelphia, Pennsylvania, United States
• Zydus US004 — Houston, Texas, United States
• Zydus US007 — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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