Study identifier:D961HC00007
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A single-centre, open, randomised, three-way cross-over drug-drug interaction study of Esomeprazole (D961H) capsule and loxoprofen tablet after repeated oral administration in Japanese healthy male subjects
Healthy
Phase 1
Yes
Esomeprazole (D961H), Loxoprofen
Male
30
Interventional
20 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of this study is to evaluate the pharmacokinetic profile of Esomeprazole (D961H) during repeated oral administration with and without co-administration of loxoprofen and the pharmacokinetic profile of loxoprofen during repeated oral administration with and without co-administration of Esomeprazole (D961H).
Location
Location
Osaka-city, Osaka, Japan
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: Esomeprazole (D961H) 20mg Other Name: Nexium |
Active Comparator: 2 | Drug: Loxoprofen 60mg tablet Other Name: Loxonin |
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