FDA Grants Orphan Drug Status To Two New Therapies In a Row, And These Two Groups Of Patients Are Expected To Benefit!
New Drug For IDH1 Mutation/Relapsed/Refractory Acute Myeloid Leukaemia With Good Complete Remission Rates And Manageable Toxicity
US National Children's Hospital
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For Fatal Rhabdomyosarcoma, New Atr Inhibitors May Hold Therapeutic Promise
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