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
| Type | Name | Description |
|---|---|---|
| DRUG | PA32540 | |
| DRUG | aspirin component of PA32540 | The 325 mg aspirin component of PA32540 |
| DRUG | Ecotrin | 325 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.