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NCT00778024 · ClinicalTrials.gov registry record · NA
Bioequivalence Study of Fluoxetine HCL 40 mg Capsules Under Fasting Conditions
A NA study, sponsored by Ranbaxy Laboratories Limited.
- Completed
- Registry status
- NA
- Development phase
- 36
- Enrollment target
NCT00778024: Completed NA study, sponsored by Ranbaxy Laboratories Limited.
NCT00778024 is a NA study that has completed, run by Ranbaxy Laboratories Limited. The registered enrollment target is 36 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00778024, a NA study, has completed, sponsored by Ranbaxy Laboratories Limited.
- COMPLETED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
Study Summary
The objective of this study is to compare the relative bioavailability of fluoxetine HCL 40 mg capsules (by Ranbaxy Laboratories Limited) with that of PROZAC® 40 mg capsules (by Dista Products Company) following a single oral dose (1 x 40 mg capsule) in healthy, adult subjects under fasting conditions
Interventions
- DRUG fluoxetine HCL 40 mg capsules
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2003-08 |
| Est. Completion | 2003-12 |
| Phase | NA |
What the finished NCT00778024 record still lists
NCT00778024 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which fluoxetine HCL 40 mg capsules is the first listed.
NCT00778024 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00778024 about?
NCT00778024 is a clinical study titled "Bioequivalence Study of Fluoxetine HCL 40 mg Capsules Under Fasting Conditions". The objective of this study is to compare the relative bioavailability of fluoxetine HCL 40 mg capsules (by Ranbaxy Laboratories Limited) with that of PROZAC® 40 mg capsules (by Dista Products Company) following a single oral dose (1 x 40 mg capsule) in healthy, adult subjects under fasting conditio...
What is the current status of trial NCT00778024?
This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2003-08. Estimated completion is 2003-12.
What interventions are being tested in trial NCT00778024?
The interventions under investigation include: fluoxetine HCL 40 mg capsules (DRUG).
Who is sponsoring clinical trial NCT00778024?
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 NCT00778024's enrollment target sits among peer trials
36 1541st of 2000 higher than 437 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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