400
Participants
Start Date
March 3, 2021
Primary Completion Date
February 28, 2023
Study Completion Date
December 31, 2023
filgotinib 200mg/day
Patients will be randomized in a 1:1 ratio to the administration of filgotinib 200mg/day or subcutaneous tocilizumab 162mg/biweekly switched from MTX ± other csDMARDs throughout the study period.
subcutaneous tocilizumab 162mg/biweekly
Patients will be randomized in a 1:1 ratio to the administration of filgotinib 200mg/day or subcutaneous tocilizumab 162mg/biweekly switched from MTX ± other csDMARDs throughout the study period.
RECRUITING
Nagasaki University Hospital, Nagasaki
Collaborators (1)
Gilead Sciences
INDUSTRY
Atsushi Kawakami
OTHER