Sitagliptin Metformin/PPARg Agonist Combination Therapy Add-on (0431-052)

PHASE3CompletedINTERVENTIONAL
Enrollment

262

Participants

Timeline

Start Date

June 12, 2006

Primary Completion Date

September 25, 2007

Study Completion Date

June 11, 2008

Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG

sitagliptin

Sitagliptin 100mg tablet each day for 54 weeks. All subjects will be given placebo to sitagliptin for a 2 week period.

DRUG

Comparator: Placebo

Placebo to sitagliptin 100mg tablet each day for 54 weeks.

DRUG

rosiglitazone

Subjects taking 4mg or greater rosiglitazone at screening will enter a 6 week stable dose period followed by a 54 week treatment period. Subjects who are taking less than 4mg/day or no rosiglitazone at screening will be titrated to a stable dose of at least 4mg over a a maximum of 8 weeks followed by a dose stable period of up to 12 weeks then a 54 week treatment period. Total treatment will be up to 77 weeks.

DRUG

metformin

Subjects taking 1500mg or greater metformin at screening will enter a 6 week stable dose period followed by a 54 week treatment period. Subjects who are taking less than 1500mg/day or no metformin at screening will be titrated to a stable dose of at least 1500mg over a a maximum of 8 weeks followed by a dose stable period of up to 12 weeks then a 54 week treatment period. Total treatment will be up to 77 weeks.

DRUG

glipizide

Subjects not meeting specific glycemic controls during the 54-week treatment period will use glipizide as rescue therapy. Glipizide will be titrated in 5mg doses up to a maximum 40mg each day. (In Canada, the rescue therapy will be a sulfonylurea agent marketed in that country.)

All Listed Sponsors
lead

Merck Sharp & Dohme LLC

INDUSTRY

NCT00350779 - Sitagliptin Metformin/PPARg Agonist Combination Therapy Add-on (0431-052) | Biotech Hunter | Biotech Hunter