Study identifier:D1140C00015
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Single-Center, Randomized, Double-Blind, Placebo-Controlled, Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD7325 When Given in Multiple Ascending Oral Doses in Healthy Male Japanese Subjects
Healthy
Phase 1
Yes
AZD7325, Placebo
Male
48
Interventional
20 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of this study is to evaluate the safety and tolerability after repeated ascending doses of AZD7325 in Japanese healthy male subjects.
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 Low dose or placebo, twice daily | Drug: AZD7325 oral capsule, once or twice daily, 7 days Drug: Placebo oral capsule, once or twice daily, 7 days |
Experimental: 2 Low dose or placebo, once daily | Drug: AZD7325 oral capsule, once or twice daily, 7 days Drug: Placebo oral capsule, once or twice daily, 7 days |
Experimental: 3 Middle dose or placebo, twice daily | Drug: AZD7325 oral capsule, once or twice daily, 7 days Drug: Placebo oral capsule, once or twice daily, 7 days |
Experimental: 4 High dose or placebo, once daily | Drug: AZD7325 oral capsule, once or twice daily, 7 days Drug: Placebo oral capsule, once or twice daily, 7 days |
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