CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 61 enrolled
Drug / intervention
BMS-986263 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03420768
NCT03420768Phase 2Completed

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of BMS-986263 in Adults With Advanced Hepatic Fibrosis After Virologic Cure of Hepatitis C

Bristol-Myers Squibb·interventional·Posted Feb 5, 2018·Updated Feb 4, 2022

In Brief

A Phase 2 clinical trial evaluating BMS-986263 and Placebo for Hepatic Cirrhosis and Liver Fibrosis. Completed, enrolled 61 participants across 1 site.

Detailed Summary

This is a study of experimental medication BMS-986263 in adult patients with advanced hepatic fibrosis (scar tissue in the liver caused by inflammation that is far on in progress) after the patient is cured of hepatitis C (an infection caused by a virus that attacks the liver and leads to inflammation).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedFeb 5, 2018
Enrollment StartFeb 14, 2018
Primary CompletionDec 10, 2018
Study CompletionMay 28, 2019
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 8.4 years ago

Interventions

BMS-986263drug

Administered by intravenous (IV) infusion

Placeboother

Administered by intravenous (IV) infusion