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NCT06715683 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate Comparative Bioavailability of BMS-986278 in Healthy Participants
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT06715683: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT06715683 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 48 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06715683, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
This is a trial to evaluate the comparative bioavailability of BMS-986278 to-be-marketed formulation compared to the phase 3 clinical trial formulation in healthy participants.
Interventions
- DRUG BMS-986278 Batched method, Dose A
- DRUG BMS-986278 Batched method, Dose B
- DRUG BMS-986278 Continuous method
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2024-12-12 |
| Est. Completion | 2025-03-16 |
| Phase | Phase 1 |
What the finished NCT06715683 record still lists
NCT06715683 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower).
The record links to 0 conditions, and to 3 interventions - of which BMS-986278 Batched method, Dose A is the first listed.
NCT06715683 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06715683 about?
NCT06715683 is a clinical study titled "A Study to Evaluate Comparative Bioavailability of BMS-986278 in Healthy Participants". This is a trial to evaluate the comparative bioavailability of BMS-986278 to-be-marketed formulation compared to the phase 3 clinical trial formulation in healthy participants.
What is the current status of trial NCT06715683?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2024-12-12. Estimated completion is 2025-03-16.
What interventions are being tested in trial NCT06715683?
The interventions under investigation include: BMS-986278 Batched method, Dose A (DRUG), BMS-986278 Batched method, Dose B (DRUG), BMS-986278 Continuous method (DRUG).
Who is sponsoring clinical trial NCT06715683?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06715683's enrollment target sits among peer trials
48 1025th of 2000 higher than 948 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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