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RECRUITING
NCT06073860

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

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

Summary

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.

Official title: Reblozyl® (Luspatercept) Post-Marketing Surveillance in Korean Patients With Myelodysplastic Syndrome or Beta Thalassemia

Key Details

Gender

All

Age Range

19 Years - Any

Study Type

OBSERVATIONAL

Enrollment

104

Start Date

2024-03-25

Completion Date

2027-12-21

Last Updated

2024-11-06

Healthy Volunteers

Not specified

Interventions

DRUG

Luspatercept

According to the approved label

Locations (2)

Local Institution - 0001

Seoul, South Korea

Novotech Laboratory Korea Co., Ltd.

Seoul, South Korea