Bioavailability and Pharmacokinetics Study of Sirukumab in Healthy Male Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

144

Participants

Timeline

Start Date

March 31, 2014

Primary Completion Date

January 31, 2015

Study Completion Date

January 31, 2015

Conditions
Healthy
Interventions
DRUG

Sirukumab (IV infusion)

Participants will receive a single IV infusion of 100 mg sirukumab.

DRUG

Sirukumab (SC injection with PFS-U)

Participants will receive a single SC injection of 50 mg sirukumab with PFS-U.

DRUG

Sirukumab (SC injection with PFS-AI)

Participants will receive a single SC injection of 50 mg sirukumab with PFS-AI.

DRUG

Sirukumab (SC injection with PFS-U)

Participants will receive a single SC injection of 100 mg sirukumab with PFS-U.

DRUG

Sirukumab (SC injection with PFS-AI)

Participants will receive a single SC injection of 100 mg sirukumab with PFS-AI.

Trial Locations (2)

Unknown

Tempe

Lincoln

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Janssen Research & Development, LLC

INDUSTRY

NCT02079545 - Bioavailability and Pharmacokinetics Study of Sirukumab in Healthy Male Participants | Biotech Hunter | Biotech Hunter