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Roche has announced that the FDA has granted Priority Review to two of its drugs – personalised lung cancer medicine entrectinib and lymphoma treatment polatuzumab vedotin.
Genentech, a subsidiary of Roche, has secured priority review status from the US Food and Drug Administration (FDA) for two of its oncology drugs, entrectinib and polatuzumab vedotin.
European regulators have awarded Ignyta’s cancer drug entrectinib Priority Medicines (PRIME) designation, potentially placing the treatment on a faster path to approval.