Dose response study in Japanese patients

Study identifier:D6160L00001

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Terminated/Withdrawn

Official Title

A Randomized, Double-Blind, Multicentre, Placebo-Controlled Study to Evaluate the Efficacy, Dose-Response and Safety of Tesaglitazar Therapy in Japanese Subjects with Type 2 Diabetes

Medical condition

Type 2 Diabetes

Phase

Phase 2

Healthy volunteers

No

Study drug

Tesaglitazar

Sex

All

Actual Enrollment

250

Study type

Interventional

Age

30 Years - 80 Years

Date

Study Start Date: 01 May 2004
Primary Completion Date: -
Study Completion Date: 01 Oct 2005

Study design

Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria