Median progression free survival in the selpercatinib group was not reached and was 16.8 months in the cabozantinib/vandetanib group. The Food and Drug Administration ...
"Patients living with RET fusion-driven NSCLC represent an underserved population in need of tailored therapies that work against this targetable alteration," said Alexander Drilon, M.D.2, chief of ...
The approvals were based on data from the LIBRETTO-001 trial. The Food and Drug Administration (FDA) has granted accelerated approval to Retevmo ® (selpercatinib) for adults with locally advanced or ...
Retevmo (selpercatinib, formerly known as LOXO-292) (pronounced reh-TEHV-moh) is a highly selective and potent RET kinase inhibitor with CNS activity. Retevmo may affect both tumor cells and healthy ...
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