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Clinical Trial Summary

Phase 1b. To evaluate the safety and tolerability of subcutaneous (SC) dose administrations of Efavaleukin alfa in subjects with active rheumatoid arthritis (RA). Phase 2a. To evaluate the efficacy of Efavaleukin alfa at week 12 as measured by the American College of Rheumatology 20 percent improvement criteria (ACR 20) in adult subjects with moderate to severe RA.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03410056
Study type Interventional
Source Amgen
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date May 22, 2018
Completion date May 13, 2020