Safety and Efficacy Study of EGT0001442 in Subjects With Type 2 Diabetes Mellitus

PHASE2CompletedINTERVENTIONAL
Enrollment

151

Participants

Timeline

Start Date

December 31, 2009

Primary Completion Date

July 31, 2010

Study Completion Date

July 31, 2010

Conditions
Diabetes Mellitus Type 2
Interventions
DRUG

EGT0001442

"Segment 1 is a single center, open labeled, ascending dose study in diabetic subjects who will receive 5, 10, 20, or 50 mg of EGT0001442 capsules orally once daily for 28 days.~Segment 2 is a multi-center, double-blind, placebo-controlled parallel group study. Diabetic subjects will be randomly assigned to receive oral EGT0001442 at 5, 10, 20, or 50 mg/day for 28 days."

DRUG

Placebo capsules to match EGT0001442

"Segment 1: Not applicable.~Segment 2: Diabetic subjects will be randomly assigned to receive oral placebo once daily for 28 days."

Trial Locations (12)

Unknown

Research Site #10, Birmingham

Research Site #04, National City

Research Site #12, Denver

Research Site #07, Miami

Research Site #08, Miami

Research Site #06, Reading

Research Site #11, DeSoto

Research Site #01, San Antonio

Research Site #15, San Antonio

Research Site #03, Brampton

Research Site #13, London

Research Site #02, Mississauga

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Theracos

INDUSTRY

NCT01029704 - Safety and Efficacy Study of EGT0001442 in Subjects With Type 2 Diabetes Mellitus | Biotech Hunter | Biotech Hunter