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Real-Time Oncology Review Program May Contribute to "Clinical Uncertainty"

Real-Time Oncology Review Program May Contribute to "Clinical Uncertainty"
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Real-Time Oncology Review Program May Contribute to "Clinical Uncertainty"

Cancer drugs approved under the FDA's Real-Time Oncology Review program may not be supported by adequate trial data, researchers suggested. Cancer drugs approved under the FDA's Real-Time Oncology Review program may not be supported by adequate trial data, researchers suggested.

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Real-time-oncology

FDA Approves Genentech's Alecensa as First Adjuvant Treatment for People With ALK-Positive Early-Stage Lung Cancer

FDA Approves Genentech's Alecensa as First Adjuvant Treatment for People With ALK-Positive Early-Stage Lung Cancer
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FDA Approves New Indication for AstraZeneca and Daiichi Sankyo's Cancer Drug ENHERTU | Goodwin

​​​​​​​On April 5, the FDA granted accelerated approval to AstraZeneca and Daiichi Sankyo’s ENHERTU (trastuzumab deruxtecan) for adult patients with unresectable or metastatic.

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Syndax Presents Positive Pediatric Data from Pivotal AUGMENT-101 Trial of Revumenib in Relapsed, Refractory KMT2Ar Acute Leukemia at ASPHO Plenary Session

WALTHAM - Syndax Pharmaceuticals , a clinical stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced the presentation of positive data from the pivotal.

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