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NCT06723535 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate BMS-986278 in Participants With Normal Renal Function, Severe Renal Impairment, or End-Stage Renal Disease on Intermittent Hemodialysis

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

Completed
Registry status
Phase 1
Development phase
27
Enrollment target

NCT06723535: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT06723535 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06723535, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

The purpose of this study is to assess the effect of severe renal impairment (RI) and end-stage renal disease (ESRD) with intermittent hemodialysis (IHD) on the pharmacokinetics and safety of BMS-986278. This study plans to use a staged design based on RI severity.

Interventions

  • DRUG BMS-986278

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2024-12-07
Est. Completion 2025-09-19
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT06723535 record still lists

NCT06723535 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 1 intervention - of which BMS-986278 is the first listed.

NCT06723535 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06723535 about?

NCT06723535 is a clinical study titled "A Study to Evaluate BMS-986278 in Participants With Normal Renal Function, Severe Renal Impairment, or End-Stage Renal Disease on Intermittent Hemodialysis". The purpose of this study is to assess the effect of severe renal impairment (RI) and end-stage renal disease (ESRD) with intermittent hemodialysis (IHD) on the pharmacokinetics and safety of BMS-986278. This study plans to use a staged design based on RI severity.

What is the current status of trial NCT06723535?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2024-12-07. Estimated completion is 2025-09-19.

What interventions are being tested in trial NCT06723535?

The interventions under investigation include: BMS-986278 (DRUG).

Who is sponsoring clinical trial NCT06723535?

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 NCT06723535's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 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 NCT06723535, the US trial registry maintained by the National Library of Medicine. NCT06723535 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.