Study of the Clinical Activity, Safety, and Tolerability of SRT2104 in Subjects With Moderate to Severe Plaque-Type Psoriasis

PHASE2CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

June 7, 2010

Primary Completion Date

November 9, 2011

Study Completion Date

November 9, 2011

Conditions
Psoriasis
Interventions
DRUG

Placebo

For the placebo product, the SRT2104 drug substance will be replaced by microcrystalline cellulose (Avicel® PH 105) to match the SRT2104 investigational product.

DRUG

SRT2104

SRT2104 drug substance is a new chemical entity which is supplied as a fine, yellowish/amber powder. The SRT2104 investigational product is prepared by packing 250 mg of micronized SRT2104 powder with no additional additives into a size 00 opaque, hard gelatin capsule, packaged in dosing bottles containing a single daily dose.

Trial Locations (8)

10016

GSK Investigational Site, New York

10065

GSK Investigational Site, New York

19103

GSK Investigational Site, Philadelphia

63117

GSK Investigational Site, St Louis

75246

GSK Investigational Site, Dallas

97223

GSK Investigational Site, Portland

98101

GSK Investigational Site, Seattle

02919

GSK Investigational Site, Johnston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Sirtris, a GSK Company

INDUSTRY

NCT01154101 - Study of the Clinical Activity, Safety, and Tolerability of SRT2104 in Subjects With Moderate to Severe Plaque-Type Psoriasis | Biotech Hunter | Biotech Hunter