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Specified Drug-Use Survey on Vedolizumab for IV Infusion 300 mg [Ulcerative Colitis]

Not Applicable
Completed
Conditions
lcerative colitis
Registration Number
JPRN-jRCT1080224534
Lead Sponsor
Takeda Pharmaceutical Company Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
All
Target Recruitment
1096
Inclusion Criteria

1. Have moderate or severe active UC
2. Have inadequate response to existing therapies

Exclusion Criteria

1.Patients with any contraindication for vedolizumab

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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