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NCT00865943 · ClinicalTrials.gov registry record · Phase 1
A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Actavis.
- Completed
- Registry status
- Phase 1
- Development phase
- 26
- Enrollment target
NCT00865943 is a Phase 1 study that has completed, run by Actavis. The registered enrollment target is 26 participants.
The verdict
NCT00865943, a Phase 1 study, has completed, sponsored by Actavis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 26 participants
- Enrollment target
Study Summary
The purpose of this study is compare the relative bioavailability of 10 mg Citalopram Hydrobromide tablets by Purepac Pharmaceutical Co with that of 10 mg CELEXATM tablets distributed and marketed by Forest Pharmaceuticals, Inc. following a single oral dose (1 x 10 mg tablet) in healthy adult volunteers under fasting conditions
Interventions
- DRUG Citalopram HBr eq. 10 mg tablets, single dose
- DRUG CELEXATM 10 mg tablets, single dose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 26 participants |
| Start Date | 2003-07 |
| Est. Completion | 2003-08 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00865943
The ClinicalTrials.gov registry entry for NCT00865943 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Actavis, which has 79 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Citalopram HBr eq. 10 mg tablets, single dose is the first listed.
NCT00865943 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00865943 about?
NCT00865943 is a clinical study titled "A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting Conditions". The purpose of this study is compare the relative bioavailability of 10 mg Citalopram Hydrobromide tablets by Purepac Pharmaceutical Co with that of 10 mg CELEXATM tablets distributed and marketed by Forest Pharmaceuticals, Inc. following a single oral dose (1 x 10 mg tablet) in healthy adult volunt...
What is the current status of trial NCT00865943?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2003-07. Estimated completion is 2003-08.
What interventions are being tested in trial NCT00865943?
The interventions under investigation include: Citalopram HBr eq. 10 mg tablets, single dose (DRUG), CELEXATM 10 mg tablets, single dose (DRUG).
Who is sponsoring clinical trial NCT00865943?
This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.
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