FDA Approves Romiplostim for Paediatric Patients with Immune Thrombocytopenia
Approval is based on results from two double-blind placebo-controlled clinical trials
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Approval is based on results from two double-blind placebo-controlled clinical trials
New indication concerns the treatment of newly diagnosed Ph+ ALL in combination with chemotherapy
Tackling legal and ethical challenges that big data brings
Approval is based on results from the CELESTIAL trial
FDA Approves Longer-acting Calaspargase Pegol-mknl for ALL
EndoPredict, Oncotype DX Breast Recurrence Score and Prosigna are recommended, while MammaPrint and IHC4+C are not
CD123-directed cytotoxin is indicated in adults and in paediatric patients
A series of articles published in the Nature Medicine highlight new technologies that are transforming medicine and healthcare
Approval is based on results from the KEYNOTE-017 study
Patients should be selected for therapy based on an FDA-approved companion diagnostic
Herzuma is indicated for the treatment of HER2-overexpressing breast cancer
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