AZD2624 Multiple Ascending Dose Study in Japan - JMAD

Study identifier:D0970C00006

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase I, Single-Center, Randomized, Double-Blind, Placebo-Controlled, Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD2624 when given in multiple ascending oral doses in young healthy male Japanese subjects

Medical condition

Healthy, Safety

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD2624, Placebo

Sex

Male

Actual Enrollment

30

Study type

Interventional

Age

20 Years - 45 Years

Date

Study Start Date: 01 May 2008
Primary Completion Date: -
Study Completion Date: 01 Aug 2008

Study design

Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Double Blind
Primary Purpose: Other

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria