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NCT01264289 · ClinicalTrials.gov registry record · Phase 1
Bioequivalence Study of Finasteride 5 mg Tablet Formulations Under Fasting Conditions
A Phase 1 study, sponsored by Dr. Reddy's Laboratories Limited.
- Completed
- Registry status
- Phase 1
- Development phase
- 26
- Enrollment target
NCT01264289: Completed Phase 1 study, sponsored by Dr. Reddy's Laboratories Limited.
NCT01264289 is a Phase 1 study that has completed, run by Dr. Reddy's Laboratories Limited. The registered enrollment target is 26 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01264289, a Phase 1 study, has completed, sponsored by Dr. Reddy's Laboratories Limited.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 26 participants
- Enrollment target
Study Summary
The objective of this study was to evaluate the relative bioavailability of the test formulation of finasteride 5 mg tablets (Dr. Reddy's Laboratories Limited) with the reference formulation PROSCAR® 5 mg Tablet (Merck \& Co., Inc.)under fasting conditions in healthy adult male subjects.
Interventions
- DRUG Finasteride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 26 participants |
| Start Date | 2006-11 |
| Est. Completion | 2006-11 |
| Phase | Phase 1 |
What the finished NCT01264289 record still lists
NCT01264289 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 26 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower).
The record links to 0 conditions, and to 1 intervention - of which Finasteride is the first listed.
NCT01264289 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01264289 about?
NCT01264289 is a clinical study titled "Bioequivalence Study of Finasteride 5 mg Tablet Formulations Under Fasting Conditions". The objective of this study was to evaluate the relative bioavailability of the test formulation of finasteride 5 mg tablets (Dr. Reddy's Laboratories Limited) with the reference formulation PROSCAR® 5 mg Tablet (Merck \& Co., Inc.)under fasting conditions in healthy adult male subjects.
What is the current status of trial NCT01264289?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2006-11. Estimated completion is 2006-11.
What interventions are being tested in trial NCT01264289?
The interventions under investigation include: Finasteride (DRUG).
Who is sponsoring clinical trial NCT01264289?
This trial is sponsored by Dr. Reddy's Laboratories Limited, which has 52 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01264289's enrollment target sits among peer trials
26 1482nd of 2000 higher than 506 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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