Study identifier:D9770C00012
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised, double-blind, multicentre dose-finding Phase IIb study for up to 8 weeks’ treatment with AZD0865 25, 50, 75 mg and esomeprazole 40 mg, given orally once daily for the healing of erosive esophagitis in adult subjects with GERD with erosive esophagitis according to the LA classification in adult subjects.
GERD with 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
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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 40 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, Newfoundland and Labrador, Canada
Location
Vancouver, BC, Canada
Location
Montreal, Quebec, Canada
Location
Saskatoon, SK, Canada
Location
Mississauga, ON, Canada
Arms | Assigned Interventions |
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