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NCT00821496 · ClinicalTrials.gov registry record · Phase 1
Evaluate the Effect of VI-0521 on the Pharmacokinetics of Oral Contraceptive in Healthy Female Subjects
A Phase 1 study, sponsored by VIVUS.
- Completed
- Registry status
- Phase 1
- Development phase
- 20
- Enrollment target
NCT00821496: Completed Phase 1 study, sponsored by VIVUS.
NCT00821496 is a Phase 1 study that has completed, run by VIVUS. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00821496, a Phase 1 study, has completed, sponsored by VIVUS.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 20 participants
- Enrollment target
Study Summary
This study is desgigned to look at the effect of multiple dosing administration of VI-0521 on Oral Contraceptive medication.
Interventions
- DRUG ethinyl estradiol, norethindrone, VI-0521
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2009-01 |
| Est. Completion | 2009-04 |
| Phase | Phase 1 |
What the finished NCT00821496 record still lists
NCT00821496 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 1 intervention - of which ethinyl estradiol, norethindrone, VI-0521 is the first listed.
NCT00821496 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00821496 about?
NCT00821496 is a clinical study titled "Evaluate the Effect of VI-0521 on the Pharmacokinetics of Oral Contraceptive in Healthy Female Subjects". This study is desgigned to look at the effect of multiple dosing administration of VI-0521 on Oral Contraceptive medication.
What is the current status of trial NCT00821496?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2009-01. Estimated completion is 2009-04.
What interventions are being tested in trial NCT00821496?
The interventions under investigation include: ethinyl estradiol, norethindrone, VI-0521 (DRUG).
Who is sponsoring clinical trial NCT00821496?
This trial is sponsored by VIVUS, which has 35 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00821496's enrollment target sits among peer trials
20 1629th of 2000 higher than 285 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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