Study identifier:D6160C00028
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A 52-week Randomized, Double-Blind, Parallel-Group, Multi-Centre, Active-Controlled (Glibenclamide) Study to Evaluate the Efficacy, Safety and Tolerability of Tesaglitazar Therapy when Administered to Patients with Type 2 Diabetes
Type 2 Diabetes
Phase 3
No
Tesaglitazar, Glibenclamide
All
580
Interventional
18 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 52-week randomized, double-blind, parallel-group, multi-center, active-controlled (glibenclamide) study of tesaglitazar in patients with type 2 diabetes, not adequately controlled on diet and lifestyle advice alone during the run-in period. The study comprises a 6 week placebo single blind run in period followed by a 52-week double blind treatment period and a 3-week follow-up period. Tesaglitazar and glibenclamide will be titrated to optimal effect or highest tolerable dose during the first 12 weeks.
Location
Location
Antwerpen, Belgium
Location
Braine-L'alleud, Belgium
Location
Hasselt, Belgium
Location
Liege, Belgium
Location
Merksem, Belgium
Location
Sint-Gillis-Waas, Belgium
Location
Steenokkerzeel, Belgium
Location
Shatin, N.T., Hong Kong
Arms | Assigned Interventions |
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