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NCT00864760 · ClinicalTrials.gov registry record · Phase 1
A Relative Bioavailability Study of Gabapentin 800 mg Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Actavis.
- Completed
- Registry status
- Phase 1
- Development phase
- 30
- Enrollment target
NCT00864760 is a Phase 1 study that has completed, run by Actavis. The registered enrollment target is 30 participants.
The verdict
NCT00864760, a Phase 1 study, has completed, sponsored by Actavis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 30 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 400 mg (2 x 400 mg) NEURONTIN® by Parke-Davis under fasting conditions.
Interventions
- DRUG Gabapentin 800 mg tablets, single dose (1 tablet)
- DRUG NEURONTIN® 400 mg capsules, single dose (2 capsules)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 1999-06 |
| Est. Completion | 1999-06 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00864760
The ClinicalTrials.gov registry entry for NCT00864760 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 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 (1 tablet) is the first listed.
NCT00864760 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00864760 about?
NCT00864760 is a clinical study titled "A Relative Bioavailability Study of Gabapentin 800 mg Tablets 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 400 mg (2 x 400 mg) NEURONTIN® by Parke-Davis under fasting conditions.
What is the current status of trial NCT00864760?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 1999-06. Estimated completion is 1999-06.
What interventions are being tested in trial NCT00864760?
The interventions under investigation include: Gabapentin 800 mg tablets, single dose (1 tablet) (DRUG), NEURONTIN® 400 mg capsules, single dose (2 capsules) (DRUG).
Who is sponsoring clinical trial NCT00864760?
This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.
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