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NCT00878020 · ClinicalTrials.gov registry record · Phase 1
Safety Study to Evaluate BMS-830216 in Healthy Subjects
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT00878020: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT00878020 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
NCT00878020, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety profile, tolerability, and pharmacokinetics of single oral doses from 10 mg up to 1200 mg of BMS-830216 (pro-drug of BMS-819881) in healthy subjects
Interventions
- DRUG Placebo
- DRUG BMS-830216
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2009-05 |
| Est. Completion | 2009-09 |
| Phase | Phase 1 |
What the finished NCT00878020 record still lists
NCT00878020 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 2 interventions - of which Placebo is the first listed.
NCT00878020 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00878020 about?
NCT00878020 is a clinical study titled "Safety Study to Evaluate BMS-830216 in Healthy Subjects". The purpose of this study is to evaluate the safety profile, tolerability, and pharmacokinetics of single oral doses from 10 mg up to 1200 mg of BMS-830216 (pro-drug of BMS-819881) in healthy subjects
What is the current status of trial NCT00878020?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2009-05. Estimated completion is 2009-09.
What interventions are being tested in trial NCT00878020?
The interventions under investigation include: Placebo (DRUG), BMS-830216 (DRUG).
Who is sponsoring clinical trial NCT00878020?
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 NCT00878020'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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