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NCT00779233 · ClinicalTrials.gov registry record · NA
Bioequivalence Study of Zidovudine 300 mg Tablets, USP Under Fasting Conditions
A NA study, sponsored by Ranbaxy Laboratories Limited.
- Completed
- Registry status
- NA
- Development phase
- 32
- Enrollment target
NCT00779233: Completed NA study, sponsored by Ranbaxy Laboratories Limited.
NCT00779233 is a NA study that has completed, run by Ranbaxy Laboratories Limited. The registered enrollment target is 32 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00779233, a NA study, has completed, sponsored by Ranbaxy Laboratories Limited.
- COMPLETED
- Registry status
- NA
- Development phase
- 32 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the relative bioavailability of the test formulation of Zidovudine 300 mg tablets with an already marketed reference formulation RETROVIR ® 300 mg tablets (GlaxoSmithKline), under fasted conditions in healthy male and female adult subjects.
Interventions
- DRUG Zidovudine tablets 300 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2004-09 |
| Est. Completion | 2004-10 |
| Phase | NA |
What the finished NCT00779233 record still lists
NCT00779233 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 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 1 intervention - of which Zidovudine tablets 300 mg is the first listed.
NCT00779233 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00779233 about?
NCT00779233 is a clinical study titled "Bioequivalence Study of Zidovudine 300 mg Tablets, USP Under Fasting Conditions". The purpose of this study is to evaluate the relative bioavailability of the test formulation of Zidovudine 300 mg tablets with an already marketed reference formulation RETROVIR ® 300 mg tablets (GlaxoSmithKline), under fasted conditions in healthy male and female adult subjects.
What is the current status of trial NCT00779233?
This trial is currently completed. It is a NA study. The enrollment target is 32 participants. The study started on 2004-09. Estimated completion is 2004-10.
What interventions are being tested in trial NCT00779233?
The interventions under investigation include: Zidovudine tablets 300 mg (DRUG).
Who is sponsoring clinical trial NCT00779233?
This trial is sponsored by Ranbaxy Laboratories Limited, which has 44 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00779233's enrollment target sits among peer trials
32 1578th of 2000 higher than 409 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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