A Clinical Study to Assess the Safety and Pharmacokinetics of SRT2379 in Normal Healthy Male Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

December 7, 2009

Primary Completion Date

August 6, 2010

Study Completion Date

August 6, 2010

Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG

SRT2379

SRT2379 will be supplied as hard gelatin capsules, with each containing 25 mg or 250 mg of SRT2379 free base equivalent (31 or 310 mg of SRT2379 monosuccinate) without any additive.

DRUG

Placebo

For placebo product, the SRT2379 drug substance will be replaced by Microcrystalline Cellulose (Avicel® PH 200) to match the SRT2379 investigational product.

Trial Locations (1)

CF48 4DR

GSK Investigational Site, Merthyr Tydfill

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01018628 - A Clinical Study to Assess the Safety and Pharmacokinetics of SRT2379 in Normal Healthy Male Volunteers | Biotech Hunter | Biotech Hunter