"TAKE TIME Pioglitazone Reverses Defects in Mitochondrial Biogenesis in Patients With T2DM"

PHASE4CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

December 31, 2007

Study Completion Date

December 31, 2007

Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG

Pioglitazone

During the double-blind, 12 weeks treatment period, subjects will self-administer study medication (pioglitazone or equivalent volume of placebo) 30 mg/day each morning. The dose of pioglitazone will be increased to 45 mg/day after 4 weeks if the fasting plasma glucose is higher than 100mg/dl or the HbA1C is higher than 7%. This dose has proven tolerability, safety and efficacy for type 2 diabetes and has previously been used at the Pennington Center in studies on pioglitazone.

Trial Locations (1)

70808

Pennington Biomedical Research Center, Baton Rouge

All Listed Sponsors
collaborator

Takeda Pharmaceuticals North America, Inc.

INDUSTRY

lead

Pennington Biomedical Research Center

OTHER

NCT00402012 - "TAKE TIME Pioglitazone Reverses Defects in Mitochondrial Biogenesis in Patients With T2DM" | Biotech Hunter | Biotech Hunter