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Expert Interview
Slingshot members are talking to an expert! The topic is:
Discussing the FDA Approval of Bristol Myers Squibb’s Reblozyl (luspatercept-aamt) as First-Line Treatment of Anemia in Adults with Lower-Risk Myelodysplastic Syndromes (MDS) Who May Require Transfusions
Ticker(s): BMYWho's the expert?
Institution: Medical College of Wisconsin
- Staff physician at the Medical College of Wisconsin, board certified in Internal Medicine, Hematology, Medical Oncology.
- Currently manages 2 newly diagnosed FLT3-ITD Positive AML patients and is familiar with the results of the QuANTUM-First trial which the FDA based their approval of Vanflyta from
- Extensive experience in Blood Disorders and Lymphatic System Disorders and affiliated with medical facilities Froedtert Hospital and Froedtert Menomonee Falls Hospital.
Interview GoalThis call will focus on the results rom the Phase 3 COMMANDS trial comparing the efficacy and safety of Bristol Myers' luspatercept vs epoetin alfa in patients with transfusion dependent LR-MDS
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Reason
*Slingshot Insights provides access to information, not investment advice. We work to support you and facilitate access to experts; however we are not responsible for monitoring calls for the disclosure of MNPI. You should obtain financial, legal and tax advice from your qualified and licensed advisers before deciding to invest in any security.
