Study identifier:D0190C00008
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A phase I, randomised, double-blind, placebo-controlled, parallel-group study to assess the safety, tolerability and pharmacokinetics of AZD0328 in healthy young Japanese and Caucasian male volunteers after oral single and multiple ascending doses
Healthy Volunteers
Phase 1
Yes
AZD0328
Male
64
Interventional
20 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Other
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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This study will be performed to evaluate the safety, tolerability and pharmacokinetics of single and multiple doses of AZD0328 when administered to Japanese and Caucasian healthy male volunteers.
Location
Location
London, United Kingdom
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: AZD0328 Oral solution A single dose Day 1 followed by once daily doses on Day 3-7 |
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