Xeljanz Special Investigation for Long-term Use in UC Patients

NCT03643211 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2016

Last updated 2024-10-08

Study results available
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Summary

Secondary data collection study: safety and effectiveness of Xeljanz in UC patients under Japanese medical practice

Conditions

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
0 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-06-08
Primary Completion
2022-11-10
Completion
2022-11-10

Countries

  • Japan

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03643211 on ClinicalTrials.gov