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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This is a study in Japanese healthy volunteers to determine the safety and tolerability of the compound, AZD5069. It will also assess how the body handles the drug and how it responds to the drug following single and multiple doses up to 11 days.
Location
Location
CROYDON, United Kingdom
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: AZD5069 Oral suspension |
Placebo Comparator: 2 | Drug: Placebo Oral suspension |
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