Study identifier:D9770C00011
ClinicalTrials.gov identifier:NCT00206284
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 Apr 2025 by AstraZeneca
AstraZeneca
-
The primary objective is to compare the efficacy between three doses of AZD0865 (25, 50 and 75 mg). The secondary objectives are to compare the efficacy between the three doses of AZD0865 and esomeprazole 20 mg and to evaluate the safety and tolerability of AZD0865.
Location
Location
Hamilton, ON, Canada
Location
Levis, QC, Canada
Location
Quebec, Quebec, Canada
Location
St. John's, Canada
Location
Vancouver, BC, Canada
Location
Montreal, QC, Canada
Location
Saskatoon, SK, Canada
Location
Mississauga, ON, Canada
Arms | Assigned Interventions |
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