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
| Type | Name | Description |
|---|---|---|
| DRUG | pantoprazole |
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.