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NCT00865423 · ClinicalTrials.gov registry record · Phase 1
A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Conditions
A Phase 1 study, sponsored by Actavis.
- Completed
- Registry status
- Phase 1
- Development phase
- 28
- Enrollment target
NCT00865423 is a Phase 1 study that has completed, run by Actavis. The registered enrollment target is 28 participants.
The verdict
NCT00865423, a Phase 1 study, has completed, sponsored by Actavis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 28 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the relative bioavailability of 800 mg Gabapentin Tablets by Purepac Pharmaceutical Co. with that of 800 mg NEURONTIN® Tablets by Parke-Davis following a single oral dose (1 x 800 mg) in healthy adult volunteers under fasting conditions.
Interventions
- DRUG Gabapentin 800 mg Tablets, single dose
- DRUG NEURONTIN® 800 mg Tablets, single dose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2001-02 |
| Est. Completion | 2001-03 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00865423
The ClinicalTrials.gov registry entry for NCT00865423 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 28 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 Gabapentin 800 mg Tablets, single dose is the first listed.
NCT00865423 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00865423 about?
NCT00865423 is a clinical study titled "A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Conditions". The purpose of this study is to compare the relative bioavailability of 800 mg Gabapentin Tablets by Purepac Pharmaceutical Co. with that of 800 mg NEURONTIN® Tablets by Parke-Davis following a single oral dose (1 x 800 mg) in healthy adult volunteers under fasting conditions.
What is the current status of trial NCT00865423?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2001-02. Estimated completion is 2001-03.
What interventions are being tested in trial NCT00865423?
The interventions under investigation include: Gabapentin 800 mg Tablets, single dose (DRUG), NEURONTIN® 800 mg Tablets, single dose (DRUG).
Who is sponsoring clinical trial NCT00865423?
This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.
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