Saroglitazar Magnesium in Patients With Nonalcoholic Fatty Liver Disease and/or Nonalcoholic Steatohepatitis

Completed · Phase 2 · Has a placebo group

Conditions studied: Non-Alcoholic Fatty Liver Disease, Nonalcoholic Steatohepatitis

In brief

This is a randomized, double-blind, placebo-controlled study in up to 104 patients with a diagnosis of Non-alcoholic fatty Liver disease (NAFLD) and/or Non-alcoholic steatohepatitis (NASH). The study will be conducted over a period of up to 22 weeks and will include an optional Prescreening, Screening (Days -35 to -7) Phase, a 16-week Treatment Phase following randomization on Day 1. Patients will be randomly assigned in a ratio of 1:1:1:1 to receive Saroglitazar Magnesium 1mg or 2 mg or 4 mg or matching placebo once daily in the morning before breakfast for 16 Weeks. The primary endpoint of the study is percentage change from baseline in serum Alanine transaminase (ALT) levels at Week 16 in the Saroglitazar Magnesium groups as compared to the placebo group.

Key facts

Study ID

NCT03061721

Run by

Zydus Therapeutics Inc.

People needed

106

Starts

2017-04-06

Expected to finish

2019-08-22

Last updated by the study team

2024-10-24

Who can join

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

You may qualify if…

• Males or females, 18 to 75 years of age, with body mass index (BMI) ≥ 25 kg/m\^2.
• Documented diagnosis of NAFLD established either by imaging (ultrasound, computed tomography [CT] scan or Magnetic resonance imaging [MRI]) or liver biopsy showing NASH or simple steatosis, within the 24 months preceding Visit 1. The diagnosis of NAFLD is made according to the American Association for the Study of Liver Diseases (AASLD) criteria (Chalasani et al. Hepatology 2012; 55:2005-2023).
• ALT level of ≥50 U/L at Visit 1 and Visit 2 with ≤30% variance between the levels at Visit 1 and Visit 2.
• Patient's demonstration of understanding of study requirements and treatment procedures, willingness to comply with all protocol-required evaluations; provision of written informed consent before any study specific tests or procedures are performed.

You may not qualify if…

• Consumption of > 3 units of alcohol per day (> 21 units per week) if male and > 2 units of alcohol per day (>14 units per week) if female for at least 3 consecutive months in the 5 years preceding Visit 1 (Note: 1 unit = 12 ounces of beer, 4 ounces of wine or 1 ounce of spirits/hard liquor).
• Presence of alternative causes of fatty liver, including:
• Weight change >5% within the 3 months preceding Visit 1
• Total parenteral nutrition, starvation or protein-calorie malnutrition within the 90 days preceding Visit 1.
• Use of drugs associated with NAFLD for more than 12 consecutive weeks in the 1 year before Visit 1, including amiodarone, tamoxifen, methotrexate, systemic glucocorticoids, anabolic steroids, tetracycline, estrogens in doses higher than used in oral contraceptives, vitamin A, L asparaginase, valproate, chloroquine or antiretroviral drugs
• Initiation of vitamin E at doses > 100 IU/day, or multivitamins containing > 100 IU/day of vitamin E in the 3 months preceding Visit 1.
• Use of drugs with potential effect on NASH such as ursodeoxycholic acid, S-adenosylmethionine (SAM-e), betaine, pentoxifylline, obeticholic acid or milk thistle in the 3 months prior to Visit 1.
• Changing doses of statins (simvastatin, pitavastatin, pravastatin, atorvastatin, fluvastatin, lovastatin, rosuvastatin) or fibrates (clofibrate, fenofibrate) in the 3 months preceding Visit 1.
• Use of thiazolidinediones (pioglitazone, rosiglitazone).
• Use of drugs that are known Cytochrome P4502C8 (CYP2C8) inhibitors/substrate
• History of bowel surgery (gastrointestinal (bariatric) surgery or undergoing evaluation for bariatric surgery for obesity, extensive small-bowel resection or orthotopic liver transplant (OLT) or listed for OLT.
• History of other chronic liver disease (chronic hepatitis C, (HCV) infection, irrespective of their mRNA HCV assay status or active hepatitis B infection, (i.e., serum positive for hepatitis B surface antigen) or autoimmune hepatitis, cholestatic and metabolic liver diseases) or hemochromatosis
• Patient has known cirrhosis, either based on clinical criteria or liver histology.
• Patient with Internation Normalised Ratio (INR) >1.3.
• Type 1 diabetes mellitus.
• Poorly controlled type 2 diabetes mellitus, i.e., glycosylated hemoglobin (HbA1c) > 9%.
• Unstable cardiovascular disease, including:
• unstable angina, (i.e., new or worsening symptoms of coronary heart disease within the 3 months preceding Visit 1), acute coronary syndrome within the 6 months preceding Visit 1, acute myocardial infarction within the 3 months preceding Visit 1 or heart failure of New York Heart Association class (III - IV) or worsening congestive heart failure, or coronary artery intervention, within the 6 months preceding Visit 1
• history of (within 3 months preceding Visit 1) or current unstable cardiac dysrhythmias
• uncontrolled hypertension (systolic blood pressure [BP] > 160 mmHg and/or diastolic BP > 100 mmHg)
• stroke or transient ischemic attack within the 6 months preceding Visit 1.
• History of myopathies or evidence of active muscle disease.
• History of malignancy in the 5 years preceding Visit 1 and/or active neoplasm with the exception of resolved superficial nonmelanoma skin cancer.
• Any of the following laboratory values:
• Hemoglobin < 9 g/dL

Where it is running

• Precision Research — Chula Vista, California, United States
• Cedars-Sinai Medical Center — Los Angeles, California, United States
• Catalina Research Institute — Montclair, California, United States
• California liver research institute — Pasadena, California, United States
• Precision Research — San Diego, California, United States
• University of Florida — Gainesville, Florida, United States
• Schiff Center for Liver Diseases/University of Miami — Miami, Florida, United States
• Avail Clinical Research — Orange City, Florida, United States
• Indiana University — Indianapolis, Indiana, United States
• Mercy Medical Center — Baltimore, Maryland, United States
• University of Michigan — Ann Arbor, Michigan, United States
• Awasty Research Network, LLC — Marion, Ohio, United States
• Einstein Medical Center — Philadelphia, Pennsylvania, United States
• Gastro One — Germantown, Tennessee, United States
• AIG Research — Hermitage, Tennessee, United States
• Liver Consultants — Dallas, Texas, United States
• The Liver Institute — San Antonio, Texas, United States
• Swedish Medical Center — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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