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NCT00865111 · ClinicalTrials.gov registry record · Phase 1
A Relative Bioavailability Study of Bupropion Sustained Release 150 mg Tablets Under Fasting Conditions
A Phase 1 study of Healthy, sponsored by Actavis.
- Completed
- Registry status
- Phase 1
- Development phase
- 26
- Enrollment target
- 1
- Study location
NCT00865111 is a Phase 1 study of Healthy that has completed, run by Actavis. The registered enrollment target is 26 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00865111, a Phase 1 study of Healthy, has completed, sponsored by Actavis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 26 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare the rate and extent of absorption of Abrika Bupropion 150 mg sustained release tablet to that of Wellbutrin SR sustained release tablet after a single, one-tablet dose in fasted subjects.
Conditions Studied
Interventions
- DRUG Bupropion 150 mg Extended-Released Tablet, single dose
- DRUG Wellbutrin SR® 150 mg Sustained-Release Tablet, single dose
Study Locations (1)
Florida
- SFBC Ft. Myers, Inc. - Fort Myers
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 26 participants |
| Start Date | 2006-03 |
| Est. Completion | 2006-04 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00865111
The ClinicalTrials.gov registry entry for NCT00865111 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, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The listed sponsor is Actavis, which has 79 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 2 interventions - of which Bupropion 150 mg Extended-Released Tablet, single dose is the first listed.
NCT00865111 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT00865111 about?
NCT00865111 is a clinical study titled "A Relative Bioavailability Study of Bupropion Sustained Release 150 mg Tablets Under Fasting Conditions". The purpose of this study is to compare the rate and extent of absorption of Abrika Bupropion 150 mg sustained release tablet to that of Wellbutrin SR sustained release tablet after a single, one-tablet dose in fasted subjects.
What is the current status of trial NCT00865111?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2006-03. Estimated completion is 2006-04.
What conditions does trial NCT00865111 study?
This clinical trial studies the following conditions: Healthy.
What interventions are being tested in trial NCT00865111?
The interventions under investigation include: Bupropion 150 mg Extended-Released Tablet, single dose (DRUG), Wellbutrin SR® 150 mg Sustained-Release Tablet, single dose (DRUG).
Who is sponsoring clinical trial NCT00865111?
This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00865111 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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