To assess the safety, tolerability and pharmacokinetics of AZD2820 after single ascending doses

Study identifier:D3870C00001

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A randomised, single-blind, placebo-controlled single-centre phase I study in healthy male volunteers to assess the safety, tolerability and pharmacokinetics of AZD2820 after single ascending doses

Medical condition

Healthy

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD2820, Placebo

Sex

Male

Actual Enrollment

90

Study type

Interventional

Age

20 Years - 45 Years

Date

Study Start Date: 01 May 2011
Primary Completion Date: 01 Nov 2011
Study Completion Date: 01 Nov 2011

Study design

Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Basic Science

Verification:

Verified 01 Jan 2014 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria