Specified Drug-Use Survey on Vedolizumab for IV Infusion 300 mg [Crohn's Disease]
NCT04002180 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 335
Last updated 2026-01-07
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 Crohn's disease (CD) patients in the routine clinical setting.
Conditions
Interventions
- DRUG
-
Vedolizumab (Genetical Recombination)
Vedolizumab IV infusion
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Study Director · Takeda
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-07-01
- Primary Completion
- 2026-06-30
- Completion
- 2026-06-30
Countries
- Japan
Study Locations
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