Study identifier:D1140C00010
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I,Single-center,Randomised,Double-blind,Placebo-controlled Single Ascending Dose Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD7325 in Healthy Male Japanese Subjects
Healthy Volunteer
Phase 1
Yes
AZD7325, Placebo
Male
48
Interventional
20 Years - 50 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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This is a Phase I randomized double-blind, placebo-controlled, single centre study to assess the safety, tolerability and pharmacokinetics of AZD7325 following single ascending dose administration to healthy male Japanese volunteers.
Location
Location
Glendale, CA, United States
Location
Baltimore, MD, United States
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: AZD7325 Capsule for oral, single dose |
Placebo Comparator: 2 | Drug: Placebo Placebo capsule for oral, single dose |
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