Overview

Study to Evaluate Safety, Tolerability and Efficacy of Saroglitazar Mg in Patients With Primary Biliary Cholangitis

Status:
Completed
Trial end date:
2020-08-07
Target enrollment:
Participant gender:
Summary
prospective, multicenter, randomized, double-blind, placebo-controlled study to evaluate safety, tolerability and efficacy of saroglitazar magnesium 2 mg, 4 mg in Patients with Primary Biliary Cholangitis. A total 36 subjects will be enrolled in a ratio of 1:1:1 to receive either saroglitazar magnesium 2 mg or saroglitazar magnesium 4 mg or placebo.
Phase:
Phase 2
Details
Lead Sponsor:
Zydus Discovery DMCC
Zydus Therapeutics Inc.