Special Drug-Use Surveillance Study on Vedolizumab for IV Infusion 300 mg [Ulcerative Colitis]
NCT03824561 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1110
Last updated 2025-09-11
Summary
The purpose of this survey is to evaluate the long-term safety and effectiveness of vedolizumab for intravenous (IV) infusion 300 milligrams (mg) in ulcerative colitis (UC) patients in the routine clinical setting.
Conditions
Interventions
- DRUG
-
Vedolizumab
Vedolizumab IV infusion
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Study Director · Takeda
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-02-01
- Primary Completion
- 2025-02-12
- Completion
- 2025-02-12
Countries
- Japan
Study Locations
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