← Eichor
Study identifier: NCT06825559 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluate PK & Safety of Saroglitazar in Subjects With Moderate Hepatic Impairment Due to Cholestatic Liver Disease

Condition: Cholestatic Liver Disease  ·  Sponsor: Zydus Therapeutics Inc.

PhasePhase 1
Planned participants6
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Evaluating Pharmacokinetic and safety of Saroglitazar Magnesium 1 mg when dosed on alternate days in subjects having moderate hepatic impairment with cirrhosis due to cholestatic liver disease

This description comes directly from the study's public registry record.

Talk to the study team

Farheen Shaikh  ·  +1-609-453-4751  ·  fshaikh@zydustherapeutics.com

Deven Parmar  ·  +1-609-946-9340  ·  dparmar@zydustherapeutics.com

Always discuss trial participation with your own doctor first.

Locations (1)

Zydus Site US001Indianapolis, Indiana, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06825559