Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
500

Summary

Conditions
Ulcerative Colitis
Type
Observational
Design
Observational Model: Case-OnlyTime Perspective: Prospective

Participation Requirements

Age
Younger than 125 years
Gender
Both males and females

Description

This investigation aims to examine the safety and effectiveness of Xeljanz in post-marketing clinical settings when it is administered chronically to patients with ulcerative colitis, based on the approval conditions.

This investigation aims to examine the safety and effectiveness of Xeljanz in post-marketing clinical settings when it is administered chronically to patients with ulcerative colitis, based on the approval conditions.

Tracking Information

NCT #
NCT03643211
Collaborators
Not Provided
Investigators
Study Director: Pfizer CT.gov Call Center Pfizer