NCT00865423

A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Conditions

A Relative Bioavailability Study of 800 mg Gabapentin Tablets Under Fasting Conditions

• Status: Completed
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 28 (actual)
• Sponsor: Actavis Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

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.

Detailed description

Study Type: Interventional Study Design: Randomized, single-dose, two-way crossover design under fasting conditions Official Title: A Relative Bioavailability Study of 800 mg Gabapentin Tablets Under Fasting Conditions Further study details as provided by Actavis Elizabeth LLC: Primary Outcome Measures: Rate and Extend of Absorption

Conditions

• Healthy

Interventions

Type	Name	Description
DRUG	Gabapentin 800 mg Tablets, single dose	A: Experimental Subjects received Purepac formulated products under fasting conditions
DRUG	NEURONTIN® 800 mg Tablets, single dose	B: Active comparator Subjects received Parke-Davis formulated products under fasting conditions

Timeline

• Start date: 2001-02-01
• Primary completion: 2001-02-01
• Completion: 2001-03-01
• First posted: 2009-03-19
• Last updated: 2010-08-17

Locations

1 site across 1 country: United States