Study identifier:D3550C00005
ClinicalTrials.gov identifier:N/A
EudraCT identifier:2009-018185-35
CTIS identifier:N/A
A Phase I, Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Oral AZD5069 in Healthy Japanese Subjects After Single and Multiple Ascending Doses
Healthy
Phase 1
Yes
AZD5069, Placebo
All
63
Interventional
20 Years - 65 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Jun 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: AZD5069 Oral suspension |
Placebo Comparator: 2 | Drug: Placebo Oral suspension |