Study to investigate safety, tolerability and pharmacokinetics of AZD2423 multiple doses in healthy volunteers

Study identifier:D2600C00002

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase I, Single Centre, Double-blind, Randomised, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability and Pharmacokinetics of Oral AZD2423 Solution after Multiple Ascending Doses in Young and Elderly Healthy Volunteers

Medical condition

Healthy

Phase

Phase 1

Healthy volunteers

Yes

Study drug

Part 1 - AZD2423 or Placebo, Part 2 - AZD2423, Part 3 - AZD2423

Sex

All

Actual Enrollment

74

Study type

Interventional

Age

20 Years - 80 Years

Date

Study Start Date: 01 Oct 2009
Primary Completion Date: 01 May 2010
Study Completion Date: 01 May 2010

Study design

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

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria