Clinical Trials Directory

Trials / Completed

CompletedNCT00632086

Evaluate Relative Bioavailability of PA32540 (Asa/Omeprazole), Its Aspirin Component, and Ecotrin® in Healthy Volunteers

A Phase 1, Open-Label, Randomized, 3-Way Crossover Study to Evaluate the Relative Bioavailability of a Single Oral Dose of Aspirin Administered as PA32540 (Aspirin/Omeprazole) or as the Aspirin Component of PA32540 or as Ecotrin® 325 mg in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
36 (estimated)
Sponsor
POZEN · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

Study to determine a single dose bioavailablity of PA32540 is similar to EC aspirin 325 mg with respect to salicylic acid.

Conditions

Interventions

TypeNameDescription
DRUGPA32540
DRUGaspirin component of PA32540The 325 mg aspirin component of PA32540
DRUGEcotrin325 mg Ecotrin

Timeline

Start date
2008-02-01
Primary completion
2008-02-01
Completion
2008-02-01
First posted
2008-03-10
Last updated
2008-03-10

Source: ClinicalTrials.gov record NCT00632086. Inclusion in this directory is not an endorsement.