Study identifier:D6160L00001
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
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
Type 2 Diabetes
Phase 2
No
Tesaglitazar
All
250
Interventional
30 Years - 80 Years
Allocation: Randomized
Endpoint Classification: Efficacy 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 12-week study to determine the effect on glucose and lipids, safety, and tolerability of four doses of tesaglitazar (0.25, 0.5, 0.75 and 1 mg) compared with placebo in patients with type 2 diabetes. Improvement in dyslipidemia will be evaluated. The study comprises a 2-week screening period, 4-week placebo run-in, a 12-week randomized, double blind, parallel group, multi-center, placebo-controlled treatment period, and a 3-week follow-up.
Location
Location
Fujimino, Japan
Location
Kousei, Japan
Location
Hyuga, Japan
Location
Ashino, Japan
Location
Fuchu Keijinkai, Japan
Location
Takamori, Japan
Location
Koga, Japan
Location
Saiseikai Fukuoka, Japan
Arms | Assigned Interventions |
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