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NCT04470778 · ClinicalTrials.gov registry record · Phase 1
Study to Assess the Effect of Acid-reducing Agent Famotidine on the Drug Levels of BMS-986256 in Healthy Participants
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 35
- Enrollment target
NCT04470778: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT04470778 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 35 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04470778, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 35 participants
- Enrollment target
Study Summary
The purpose of this study is to investigate the effect of gastric pH changes due to famotidine administration on the drug levels of prototype BMS-986256 tablet formulation in healthy participants.
Interventions
- DRUG Famotidine
- DRUG BMS-986256
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2020-07-20 |
| Est. Completion | 2021-03-28 |
| Phase | Phase 1 |
What the finished NCT04470778 record still lists
NCT04470778 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower).
The record links to 0 conditions, and to 2 interventions - of which Famotidine is the first listed.
NCT04470778 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04470778 about?
NCT04470778 is a clinical study titled "Study to Assess the Effect of Acid-reducing Agent Famotidine on the Drug Levels of BMS-986256 in Healthy Participants". The purpose of this study is to investigate the effect of gastric pH changes due to famotidine administration on the drug levels of prototype BMS-986256 tablet formulation in healthy participants.
What is the current status of trial NCT04470778?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2020-07-20. Estimated completion is 2021-03-28.
What interventions are being tested in trial NCT04470778?
The interventions under investigation include: Famotidine (DRUG), BMS-986256 (DRUG).
Who is sponsoring clinical trial NCT04470778?
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 NCT04470778's enrollment target sits among peer trials
35 1258th of 2000 higher than 728 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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