Last updated on February 2019

Safety and Efficacy of AMG 592 in Subjects With Active Rheumatoid Arthritis

Brief description of study

Phase 1b. To evaluate the safety and tolerability of subcutaneous (SC)dose administrations of AMG 592 in subjects with active RA.

Phase 2a. To evaluate the efficacy of AMG 592 at week 12 as measured by the American College of Rheumatology 20% improvement criteria (ACR 20) in adult subjects with moderate to severe RA.

Clinical Study Identifier: NCT03410056

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Recruitment Status: Open

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