Clinical Trials Directory

Trials / Completed

CompletedNCT01337804

A Study to Compare Omeprazole Administered as Zegerid® Powder and as Prilosec® Capsule in Healthy Participants (P08050)(CL2010-12)

A Single Dose, Comparative, Open-label, Randomized, Crossover Bioequivalence Study of Omeprazole Administered as Zegerid® Powder for Oral Suspension 20 mg and Prilosec 40 mg Capsule in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Bayer · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study compares the bioequivalence of omeprazole administered as either Zegerid® powder for oral suspension 20 mg or as Prilosec 40 mg capsule to healthy participants.

Conditions

Interventions

TypeNameDescription
DRUGomeprazole/sodium bicarbonateSingle 20 mg dose of omeprazole/sodium bicarbonate powder for oral suspension
DRUGomeprazole magnesiumSingle 40 mg capsule of omeprazole given orally

Timeline

Start date
2011-01-01
Primary completion
2011-01-01
Completion
2011-01-01
First posted
2011-04-19
Last updated
2015-02-23

Source: ClinicalTrials.gov record NCT01337804. Inclusion in this directory is not an endorsement.