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| Sponsor: | Wyeth |
|---|---|
| Information provided by: | Wyeth |
| ClinicalTrials.gov Identifier: | NCT00367614 |
Purpose
The purpose of this study is characterize the PK profile of single and multiple doses of pantoprazole in adolescents aged 12 to 16 years with Gastroesophageal Reflux Disease (GERD).
| Condition | Intervention | Phase |
|---|---|---|
|
Gastroesophageal Reflux |
Drug: pantoprazole |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Dose Comparison, Single Group Assignment, Pharmacokinetics Study |
| Official Title: | A Multicenter, Randomized, Open-Label, Single And Multiple Dose Study Of The Pharmacokinetics And Safety of Two Dose Levels of Pantoprazole Sodium Tablets In Adolescents Aged 12 Through 16 Years With A Clinical Daignosis Of GERD. |
Eligibility| Ages Eligible for Study: | 12 Years to 16 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | 3001A3-337 |
| Study First Received: | August 21, 2006 |
| Last Updated: | December 7, 2007 |
| ClinicalTrials.gov Identifier: | NCT00367614 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Adolescents GERD |
|
Deglutition Disorders Esophageal Motility Disorders Digestive System Diseases Gastrointestinal Diseases Therapeutic Uses Pantoprazole |
Anti-Ulcer Agents Gastrointestinal Agents Esophageal Diseases Gastroesophageal Reflux Pharmacologic Actions |