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NCT04766476 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Terminated
Registry status
Phase 1
Development phase
9
Enrollment target

NCT04766476: Clinical Trial Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT04766476 is a Phase 1 study that was terminated before completion, run by Bristol-Myers Squibb. The registered enrollment target is 9 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04766476, a Phase 1 study, was terminated before completion, sponsored by Bristol-Myers Squibb.

TERMINATED
Registry status
Phase 1
Development phase
9 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG BMS-963272
  • OTHER Placebo matching BMS-963272

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2021-02-24
Est. Completion 2021-08-12
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

Why NCT04766476 stopped before completion

NCT04766476 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 2 interventions - of which BMS-963272 is the first listed.

NCT04766476 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04766476 about?

NCT04766476 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-963272 in Participants With Nonalcoholic Fatty Liver Disease". 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.

What is the current status of trial NCT04766476?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 9 participants. The study started on 2021-02-24. Estimated completion is 2021-08-12.

What interventions are being tested in trial NCT04766476?

The interventions under investigation include: BMS-963272 (DRUG), Placebo matching BMS-963272 (OTHER).

Who is sponsoring clinical trial NCT04766476?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04766476's enrollment target sits among peer trials

9 1955th of 2000 higher than 42 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04766476, the US trial registry maintained by the National Library of Medicine. NCT04766476 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.