An Active Surveillance, Post-Authorization Study to Characterize the Safety of Tofacitinib in Patients With Moderately to Severely Active Ulcerative Colitis in the Real-World Setting Using Data From the United Registries for Clinical Assessment and Research (UR-CARE) in the European Union (EU)

21/07/2023
24/03/2026
EU PAS number:
EUPAS103632
Study
Planned
Documents
Study protocol
Initial protocol
English (605.65 KB - PDF) View document
Study results
Study report
Abstract of study report
English (566.98 KB - PDF) View document
Other information