Study identifier:D6160C00047
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Parallel-Group, Multi-Centre, Active-Controlled (Glibenclamide) Long-Term Extension Study to Evaluate the Safety and Tolerability of Oral Tesaglitazar Therapy in Patients with Type 2 Diabetes
Type 2 Diabetes
Phase 3
No
Tesaglitazar
All
400
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 parallel-group, multi-center, long-term extension study from the GALLANT 4 study to monitor the safety and tolerability of oral tesaglitazar compared with glibenclamide in patients with type 2 diabetes for up to 100 weeks of treatment. The total duration, including treatment and follow-up, is 103 weeks.
Location
Location
Hasselt, Belgium
Location
Liege, Belgium
Location
Sint-Gillis-Waas, Belgium
Location
Steenokkerzeel, Belgium
Location
Shatin, Hong Kong
Location
Balatonfured, Hungary
Location
Budapest, Hungary
Location
Kaposvar, Hungary
Arms | Assigned Interventions |
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