Trials / Completed

CompletedNCT00803946

Bioequivalence Study Between Two Oral Formulations of Ibuprofen 800 mg Tablets Under Fed Conditions

A Randomized, Single-Dose, Two-Way Crossover Relative Bioavailability Study of Ibuprofen Tablet Formulations in Normal, Healthy Men and Women Following Standard Meal

Status: Completed
Phase: Phase 1
Study type: Interventional
Enrollment: 30 (actual)

Sponsor: Perrigo Company · Industry
Sex: All
Age: 18 Years
Healthy volunteers: Accepted

Summary

Compare the rate and extent of absorption of two oral formulations of Ibuprofen 800 mg Tablets, administered as a 1 x 800 mg tablet, under fed conditions.

Conditions

Bioequivalency

Interventions

Type	Name	Description
DRUG	Ibuprofen Tablets, 800 mg

Timeline

Start date: 2003-11-01
Primary completion: 2003-11-01
First posted: 2008-12-08
Last updated: 2012-03-16

Source: ClinicalTrials.gov record NCT00803946. Inclusion in this directory is not an endorsement.