drugset / Trial / NCT03061721

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

NCT03061721

Phase 2 Completed 106 enrolled Zydus Therapeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2017-04-06
Primary completion
2019-08-22
Completion
2019-08-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Saroglitazar Small molecule 1 mg Oral
Subject Saroglitazar Small molecule 2 mg Oral
Subject Saroglitazar Small molecule 4 mg Oral