Overview

Safety, Tolerability, and Pharmacokinetics of GS-5745 in Subjects With Rheumatoid Arthritis

Status:
Completed
Trial end date:
2015-06-01
Target enrollment:
Participant gender:
Summary
This study is to assess the safety, tolerability, and pharmacokinetics (PK) of multiple infusions of GS-5745 in adults with rheumatoid arthritis (RA). Participants will be randomized in a 4:1 ratio to receive 1 intravenous (IV) infusion of GS-5745 or placebo every 2 weeks, for a total of 3 IV infusions.
Phase:
Phase 1
Details
Lead Sponsor:
Gilead Sciences
Treatments:
Antibodies, Monoclonal