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A Post-Marketing Surveillance Study to Assess Safety of Luspatercept in Korean Patients With Myelodysplastic Syndrome or β-thalassemia

A Post-Marketing Surveillance Study to Assess Safety of Luspatercept in Korean Patients With Myelodysplastic Syndrome or β-thalassemia

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 luspatercept in Korean participants with myelodysplastic syndrome (MDS) or beta thalassemia. Investigators will enroll participants who will begin treatment with at least 1 dose of luspatercept.

Eligibility

Inclusion Criteria:

  • Adult participants 19 years of age or older
  • Participants who will be treated with luspatercept according to the approved label in the Republic of Korea
  • Participants who sign the informed consent form

Exclusion Criteria:

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

Study details
    Myelodysplastic Syndrome
    Beta Thalassemia

NCT06073860

Bristol-Myers Squibb

13 April 2024

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