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A Post-Marketing Surveillance Study to Assess Safety of Ozanimod in Patients With Moderate to Severe Active UC in Korea

A Post-Marketing Surveillance Study to Assess Safety of Ozanimod in Patients With Moderate to Severe Active UC in Korea

Recruiting
19 years and older
All
Phase N/A
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Overview

The purpose of this observational study is to assess the real-world safety of ozanimod in Korean participants with moderate to severe active ulcerative colitis.

Eligibility

Inclusion Criteria:

  • Adult participants 19 years of age or older
  • Participants who will receive ozanimod according to the approved label after enrollment
  • Participants who sign the informed consent form voluntarily

Exclusion Criteria:

  • Participants who are prescribed ozanimod for therapeutic indications not approved in Korea
  • Participants for whom ozanimod is contraindicated as clarified in Korean prescribing information approved by Ministry of Food and Drug Safety

Study details
    Ulcerative Colitis

NCT06073873

Bristol-Myers Squibb

3 May 2024

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