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Terminated Phase 1 Interventional

A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-963272 in Participants With Nonalcoholic Fatty Liver Disease

ClinicalTrials.gov ID: NCT04766476

Public ClinicalTrials.gov record NCT04766476. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 9, 2026, 1:48 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 1b Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BMS-963272 in Participants With Nonalcoholic Fatty Liver Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety, tolerability, and drug levels of BMS-963272 compared to placebo in participants with nonalcoholic fatty liver disease (NAFLD) and high probability of advanced fibrosis.

Study identification

NCT ID
NCT04766476
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
9 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 24, 2021 (Actual)
Primary completion
Aug 12, 2021 (Actual)
Completion
Aug 12, 2021 (Actual)
Last update posted
Jun 9, 2022

2021

United States locations

U.S. sites
19
U.S. states
8
U.S. cities
17
Facility City State ZIP Site status
Cullman Clinical Trials Cullman Alabama 35055 —
Local Institution Chandler Arizona 85224 —
Arizona Liver Health - Tucson Tucson Arizona 85712 —
Local Institution Boca Raton Florida 33434 —
RecioMed Clinical Research Network Boynton Beach Florida 33472 —
Local Institution Miami Florida 33014 —
Advanced Pharma - Miami Miami Florida 33147 —
Floridian Clinical Research Miami Lakes Florida 33016 —
Local Institution Port Orange Florida 32127 —
Local Institution Bastrop Louisiana 71220 —
Local Institution Biloxi Mississippi 39532 —
Local Institution Kansas City Missouri 64131 —
Local Institution Chattanooga Tennessee 37421 —
Local Institution Germantown Tennessee 38138 —
Pinnacle Clinical Research - Austin Austin Texas 78757 —
Local Institution Edinburg Texas 78539 —
Local Institution McAllen Texas 78504 —
Local Institution San Antonio Texas 78215 —
Local Institution San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04766476, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 9, 2022 · Synced Nov 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04766476 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →