Clinical Trials Directory

Trials / Completed

CompletedNCT00383916

Study Comparing 2 Different Formulations of Pantoprazole in Healthy Adults.

An Open-Label, Single-Dose, Randomized, 2-Period, Crossover, Bioequivalence Study Between the Altana Formulation of Pantoprazole Delayed-Release Granules and the Wyeth Formulation of Pantoprazole Delayed-Release Granules in Healthy Subjects.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

A study comparing 2 different investigational formulations of pantoprazole in healthy adults.

Detailed description

open-label, single-dose, randomized, 2-period, 2-sequence, crossover, inpatient bioequivalence study

Conditions

Interventions

TypeNameDescription
DRUGpantoprazole

Timeline

Start date
2006-10-01
Completion
2006-10-01
First posted
2006-10-04
Last updated
2007-03-08

Source: ClinicalTrials.gov record NCT00383916. Inclusion in this directory is not an endorsement.