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
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: AZD0328 Oral solution A single dose Day 1 followed by once daily doses on Day 3-7 |