drugset / Trial / NCT00226330

GALLEX 6: Study to Evaluate the Safety and Tolerability of Tesaglitazar in Patients With Type 2 Diabetes Mellitus

NCT00226330 ↗

Phase 3 Terminated 1100 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

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.

Timeline

Start
2005-03
Primary completion
2006-12
Completion
2006-12

Outcome

Outcome not reported

Stopped: “The development program has been terminated”

Drugs

EvaluationDrugModalityDoseRoute
Subject Pioglitazone Small molecule 15 mg —
Subject Pioglitazone Small molecule 30 mg —
Subject Pioglitazone Small molecule 45 mg —
Subject Tesaglitazar Small molecule 0.5 mg Oral
Subject Tesaglitazar Small molecule 1 mg Oral