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

No results posted yet for this study

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

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

More Related Trials

Entities

Companies

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 NCT04002180 on ClinicalTrials.gov