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NCT00835666 · ClinicalTrials.gov registry record · Phase 1
Finasteride 5 mg Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT00835666: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00835666 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00835666, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
The objective of this study is to compare the relative bioavailability of finasteride 5 mg tablets (manufactured and distributed by TEVA Pharmaceuticals USA) with that of PROSCAR® 5 mg tablets (Merck) in healthy, adult, non-smoking, male subjects under fasting conditions.
Primary Outcome
Bioequivalence based on Cmax
Interventions
- DRUG Finasteride 5 mg tablets
- DRUG PROSCAR®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2002-06 |
| Est. Completion | 2002-06 |
| Phase | Phase 1 |
What the finished NCT00835666 record still lists
NCT00835666 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).
The record links to 0 conditions, and to 2 interventions - of which Finasteride 5 mg tablets is the first listed.
NCT00835666 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00835666 about?
NCT00835666 is a clinical study titled "Finasteride 5 mg Tablets Under Fasting Conditions". The objective of this study is to compare the relative bioavailability of finasteride 5 mg tablets (manufactured and distributed by TEVA Pharmaceuticals USA) with that of PROSCAR® 5 mg tablets (Merck) in healthy, adult, non-smoking, male subjects under fasting conditions.
What is the current status of trial NCT00835666?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2002-06. Estimated completion is 2002-06.
What interventions are being tested in trial NCT00835666?
The interventions under investigation include: Finasteride 5 mg tablets (DRUG), PROSCAR® (DRUG).
Who is sponsoring clinical trial NCT00835666?
This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00835666's enrollment target sits among peer trials
32 1296th of 2000 higher than 679 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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