drugset / Trial / NCT00814372

Evaluate Safety and Effectiveness of MBX-102 in Type 2 Diabetes Patients With Poor Glycemic Control on Metformin

NCT00814372

Phase 2 Terminated 242 enrolled Gilead Sciences
RandomizedParallel-groupTriple-blindTreatment

Summary

To define the relative efficacy, safety and tolerability profiles of oral daily MBX-102 at daily doses of 400 and 600 mg vs. placebo and Actos® 30 mg (up-titrated to 45 mg after 8 weeks) when administered for up to 24 weeks in patients inadequately controlled with a stable dose of metformin (≥ 1500 mg/day).

Timeline

Start
2008-12
Primary completion
2010-02
Completion
2010-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Arhalofenate Unknown 400 mg Oral
Subject Arhalofenate Unknown 600 mg Oral
Comparator Pioglitazone Small molecule 45 mg
Background Metformin Small molecule 1500 mg/kg