178
Participants
Start Date
October 1, 2025
Primary Completion Date
October 1, 2028
Study Completion Date
November 1, 2028
Interleukin-23 Inhibitors (IL-23i)
Adult patients will receive treatment with an interleukin-23 inhibitor (IL-23i), including guselkumab or risankizumab, as prescribed in routine clinical practice in China. This observational study does not mandate dosing, administration schedule, or concomitant medications; treatments follow standard of care. Patients will be prospectively monitored for clinical effectiveness, endoscopic outcomes, and safety over 52 weeks.
Sixth Affiliated Hospital, Sun Yat-sen University
OTHER