Study identifier:D961RC00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase III Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial of 14 Day Treatment with Esomeprazole 20 mg Once Daily in Subjects with Frequent Heartburn
Heartburn
Phase 3
No
Esomeprazole
All
341
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Mar 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Esomeprazole 20 mg | Drug: Esomeprazole Nexium 20 mg administered as 22.3 mg of esomeprasole magnesium hydrate, capsule, oral dose |
Placebo Comparator: Placebo | Drug: Esomeprazole Nexium 20 mg administered as 22.3 mg of esomeprasole magnesium hydrate, capsule, oral dose |