Study identifier:D6160C00048
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Double-Blind, Multi-Centre, Active-Controlled (15, 30, and 45 mg Pioglitazone) Long-Term Extension Study to Evaluate the Safety and Tolerability of Tesaglitazar (0.5 and 1 mg) in Patients with Type 2 Diabetes Mellitus (GALLEX 6)
Diabetes Mellitus, Type 2
Phase 3
No
Tesaglitazar, Pioglitazone
All
1100
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Safety 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 parallel-group, multi-center, long-term extension study from the GALLANT 6 study to monitor the safety and tolerability of oral tesaglitazar compared with pioglitazone in patients with type 2 diabetes for up to 104 weeks of treatment. The total duration, including treatment and follow-up, is 107 weeks.
Location
Location
Ciudad de Buenos Aires, Argentina
Location
Córdoba - Córdoba, Argentina
Location
Moron, Buenos Aires, Argentina
Location
Quilmes, Buenos Aires, Argentina
Location
Rosario, Argentina
Location
Salta - Salta, Argentina
Location
Curitiba, Brazil
Location
Fortaleza, Brazil
Arms | Assigned Interventions |
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