Symptom Assessment in Adult Patients With Erosive GERD (Gastroesophageal Reflux Disease) or enGERD (Endoscopic-Negative GERD) After Treatment With Pantoprazole (BY1023/M3-343)

2014-08-27 03:44:13 | BioPortfolio


The aim of this study is to compare investigator and patient-assessed gastroesophageal reflux disease symptoms in patients with erosive GERD or endoscopic-negative GERD (enGERD). An endoscopy will be performed at study start and study end. During the study, the patients will complete a patient-orientated, self-assessed reflux questionnaire (ReQuest™ questionnaire). The study duration consists of a baseline period (8 days) and treatment period (28 days). Pantoprazole (tablet) will be administered once daily at one dose level. The study will provide further data on safety and tolerability of pantoprazole.

Study Design

Allocation: Non-Randomized, Control: Uncontrolled, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment






Altana Pharma/Nycomed
Bondi Junction
NSW 2022





Results (where available)

View Results


Published on BioPortfolio: 2014-08-27T03:44:13-0400

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Medical and Biotech [MESH] Definitions

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