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NCT00874770 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy of Daclatasvir (BMS-790052) Plus Standard of Care (Pegylated-interferon Alpha and Ribavirin)
A Phase 2 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 2
- Development phase
- 74
- Enrollment target
NCT00874770: Completed Phase 2 study, sponsored by Bristol-Myers Squibb.
NCT00874770 is a Phase 2 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 74 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (44% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00874770, a Phase 2 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 74 participants
- Enrollment target
Study Summary
The purpose of this study is to identify 1 or more doses of daclatasvir, which when used in combination with pegylated interferon alpha and ribavirin, are safe and demonstrate sufficient anti-hepatitis C virus activity.
Primary Outcome
eRVR was defined as undetectable hepatitis C virus RNA less than the lower limit of detection (10 IU/mL) at Weeks 4 and 12.
Interventions
- DRUG Placebo
- DRUG Daclatasvir
- DRUG Peginterferon alpha-2a
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2009-06 |
| Est. Completion | 2011-01 |
| Phase | Phase 2 |
What the finished NCT00874770 record still lists
NCT00874770 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (44% lower).
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT00874770 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00874770 about?
NCT00874770 is a clinical study titled "Safety and Efficacy of Daclatasvir (BMS-790052) Plus Standard of Care (Pegylated-interferon Alpha and Ribavirin)". The purpose of this study is to identify 1 or more doses of daclatasvir, which when used in combination with pegylated interferon alpha and ribavirin, are safe and demonstrate sufficient anti-hepatitis C virus activity.
What is the current status of trial NCT00874770?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 74 participants. The study started on 2009-06. Estimated completion is 2011-01.
What interventions are being tested in trial NCT00874770?
The interventions under investigation include: Placebo (DRUG), Daclatasvir (DRUG), Peginterferon alpha-2a (DRUG).
Who is sponsoring clinical trial NCT00874770?
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 NCT00874770's enrollment target sits among peer trials
74 920th of 2000 higher than 1,077 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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