Condition: Myelodysplastic Syndrome · Beta Thalassemia · Sponsor: Bristol-Myers Squibb
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.
This description comes directly from the study's public registry record.
BMS Study Connect Contact Center www.BMSStudyConnect.com · 855-907-3286 · Clinical.Trials@bms.com
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| Local Institution - 0001 | Seoul, South Korea | Terminated |
| Novotech Laboratory Korea Co., Ltd. | Seoul, South Korea | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06073860