An active surveillance, post-authorization safety study of serious infection, malignancy, cardiovascular and other safety events of interest among patients treated with tofacitinib for moderately to severely active rheumatoid arthritis within the Spanish registry of adverse events of biological therapies and biosimilars in rheumatoid diseases (BIOBADASER) (Safety of tofacitinib in BIOBADASER)

05/09/2019
03/12/2024
EU PAS number:
EUPAS31129
Study
Ongoing
Documents
Study protocol
Initial protocol
English (1.12 MB - PDF) View document
Updated protocol
English (560.88 KB - PDF) View document
Study results
Study report
Other information