Study of Belimumab Administered Subcutaneously to Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

118

Participants

Timeline

Start Date

February 28, 2011

Primary Completion Date

September 30, 2011

Study Completion Date

September 30, 2011

Conditions
Healthy
Interventions
BIOLOGICAL

Single Dose Group: Belimumab IV 240 mg

Belimumab IV 240 mg administered on Day 0

BIOLOGICAL

Single Dose Group: Belimumab SC 2 x 120 mg

Belimumab SC 120 mg x 2 injections (equal to 240 mg) administered immediately one after the other on Day 0

BIOLOGICAL

Single Dose Group: Belimumab SC 1 x 240 mg

Belimumab SC 240 mg x 1 injection on Day 0

BIOLOGICAL

Single Dose Group: Belimumab SC 1 x 200 mg

Belimumab SC 200 mg x 1 injection on Day 0

BIOLOGICAL

Multiple Dose Group: Belimumab SC 2 x 120 mg weekly

Belimumab 120 mg x 2 injections (equal to 240 mg) administered immediately one after the other on Days 0, 7, 14, and 21

BIOLOGICAL

Multiple Dose Group: Belimumab SC 1 x 200 mg weekly

Belimumab 200 mg x 1 injection administered on Days 0, 7, 14, and 21

Trial Locations (4)

Unknown

Daytona Beach

Evansville

Dallas

Madison

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Human Genome Sciences Inc.

INDUSTRY