Non-interventional post-authorization cohort safety study evaluating the effectiveness of the additional risk minimization measures for filgotinib (Jyseleca®) use in patients with moderate to severe active rheumatoid arthritis within European registries

29/06/2022
10/03/2025
EU PAS number:
EUPAS46852
Study
Ongoing
Documents
Study protocol
Initial protocol
English (5.29 MB - PDF) View document
Updated protocol
English (1.72 MB - PDF) View document
Study results
Study report
Other information