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    Blinatumomab received U.S. Food and Drug A dministration (FDA) approval for the treatment of adult and pediatric patients with CD19-positive B-cell precursor acute lymphoblastic leukemia (ALL) in first or second complete remission with measurable residual disease (MRD) greater than or equal to 0.1%. The drug previously received accelerated approval from the FDA but was granted full approval based on data from two phase III studies. The treatment is a bispecific T-cell engager immuno-oncology therapy that

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    • The #FDA approved #binatumomab, a bispecific T-cell engager immuno-oncology therapy, for treatment of adult and pediatric patients with CD19-positive B-cell precursor #ALL in first or second complete remission with MRD greater than or equal to 0.1%. https://t.co/d8dSu9hcU6