NCT Number: NCT00383916
Study Comparing 2 Different Formulations of Pantoprazole in Healthy Adults.
A study comparing 2 different investigational formulations of pantoprazole in healthy adults.
Looking for future studies?
Notify MeKey information
Conditions
Age range
18 year–50 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
About this study
open-label, single-dose, randomized, 2-period, 2-sequence, crossover, inpatient bioequivalence study
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Men or women aged 18 to 50 years.
- Healthy as determined by the investigator.
Exclusion criteria
- History or active presence of clinically important medical disease.
- History of drug or alcohol abuse.
Treatment and study plan
Primary outcomes
-
To determine the bioequivalence of the Altana formulation of pantoprazole to the Wyeth formulation of pantoprazole delayed-release granules.
Secondary outcomes
-
To obtain additional safety and tolerability data concerning pantoprazole in healthy subjects and to assess the pharmacokinetics of the Altana formulation.
Interested in participating?
Looking for future studies?
Notify MeSponsors and collaborators
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
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.
Important dates
- Study start
- 2006
- Study completion
- 2006
- First posted
- Oct 4, 2006
- Registry last updated
- Mar 8, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Y-Balance Test Training for Ankle Function and Lower Limb Functional Performance
NCT07826312
Healthy Subjects
Aveiro, Aveiro District, Portugal
View Trial DetailsIn-Person Recruitment of Individuals to the Alzheimer's Prevention Trial (APT) Webstudy
NCT07218120
Healthy Subjects, Memory Decline
Chula Vista, California, United States
View Trial DetailsThe Effects of Urinary pH Changes on an Investigational Compound in Healthy Subjects
NCT01440478
Healthy Subjects
Leeds, United Kingdom
View Trial DetailsHigh Image Matrix CT Reconstruction
NCT02610465
Cardiac-Related Conditions, Healthy Subjects
Bethesda, Maryland, United States
View Trial Details