Study identifier:D9770C00011
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A 4-week, randomised, double-blind, multicentre, dose-finding phase IIb study with AZD0865 25, 50, 75 mg and esomeprazole 20 mg, given orally once daily for the treatment of GERD without erosive esophagitis according to the LA classification in adult subjects.
GERD without erosive esophagitis
Phase 2
No
AZD0865
All
1400
Interventional
18 Years - 70 Years
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|