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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: Completed Phase 1 study of Healthy, sponsored by Actavis.
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. According to ClinicalTrials.gov, the official US trial registry.
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 |
What the finished NCT00865111 record still lists
NCT00865111 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 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Healthy
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00865111's enrollment target sits among peer trials
26 760th of 1090 higher than 314 of 1,090 other Healthy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Healthy 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.
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