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NCT06955741 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess Drug Levels, Tolerability and Absolute Biological Availability of Single-dose of BMS-986446 in Healthy Participants

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

Completed
Registry status
Phase 1
Development phase
46
Enrollment target

NCT06955741: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT06955741 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 46 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06955741, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
46 participants
Enrollment target

Study Summary

The purpose of this study is to assess drug levels, tolerability and absolute biological availability of single subcutaneous dose of BMS-986446 in healthy participants

Interventions

  • DRUG Acetaminophen
  • DRUG Loratadine
  • DRUG BMS-986446 IV
  • DRUG BMS-986446 SC

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2025-05-05
Est. Completion 2025-09-11
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT06955741 record still lists

NCT06955741 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower).

The record links to 0 conditions, and to 4 interventions - of which Acetaminophen is the first listed.

NCT06955741 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06955741 about?

NCT06955741 is a clinical study titled "A Study to Assess Drug Levels, Tolerability and Absolute Biological Availability of Single-dose of BMS-986446 in Healthy Participants". The purpose of this study is to assess drug levels, tolerability and absolute biological availability of single subcutaneous dose of BMS-986446 in healthy participants

What is the current status of trial NCT06955741?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2025-05-05. Estimated completion is 2025-09-11.

What interventions are being tested in trial NCT06955741?

The interventions under investigation include: Acetaminophen (DRUG), Loratadine (DRUG), BMS-986446 IV (DRUG), BMS-986446 SC (DRUG).

Who is sponsoring clinical trial NCT06955741?

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 NCT06955741's enrollment target sits among peer trials

46 1058th of 2000 higher than 935 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 NCT06955741, the US trial registry maintained by the National Library of Medicine. NCT06955741 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.