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NCT03058822 · ClinicalTrials.gov registry record · Phase 1
Relative Bioavailability of BMS-931699 From Prefilled Syringe Compared to Drug in Vial
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Terminated
- Registry status
- Phase 1
- Development phase
- 5
- Enrollment target
NCT03058822: Clinical Trial Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT03058822 is a Phase 1 study that was terminated before completion, run by Bristol-Myers Squibb. The registered enrollment target is 5 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03058822, a Phase 1 study, was terminated before completion, sponsored by Bristol-Myers Squibb.
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 5 participants
- Enrollment target
Study Summary
A Phase 1, relative bioavailability study of BMS-931699 from prefilled syringe compared to drug in vial
Interventions
- DRUG BMS-931699
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2017-01-25 |
| Est. Completion | 2017-03-30 |
| Phase | Phase 1 |
Why NCT03058822 stopped before completion
NCT03058822 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 1 intervention - of which BMS-931699 is the first listed.
NCT03058822 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03058822 about?
NCT03058822 is a clinical study titled "Relative Bioavailability of BMS-931699 From Prefilled Syringe Compared to Drug in Vial". A Phase 1, relative bioavailability study of BMS-931699 from prefilled syringe compared to drug in vial
What is the current status of trial NCT03058822?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 5 participants. The study started on 2017-01-25. Estimated completion is 2017-03-30.
What interventions are being tested in trial NCT03058822?
The interventions under investigation include: BMS-931699 (DRUG).
Who is sponsoring clinical trial NCT03058822?
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 NCT03058822's enrollment target sits among peer trials
5 1989th of 2000 higher than 6 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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