FDA nods Zykadia

May 1, 2014

NOVARTIS has been granted US Food and Drug Administration (FDA) approval for Zykadia (ceritinib). This was the first therapy for patients with ALK+ non-small cell lung cancer (NSCLC) previously treated with the ALK inhibitor crizotinib, Novartis said. Zykadia demonstrated an overall response rate of 54.6% in patients with ALK+ metastatic NSCLC who have no other treatment option with a median duration of response of 7.4 months. The approval is part of the FDA’s Breakthrough Therapy designation.

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Pharmacy Daily | FDA nods Zykadia

FDA nods Zykadia

Other recent headlines

PD breaking news – 2024 PSA MIMS Credentialed Pharmacist of the Year winner announced

Dementia body’s new face

Many stores still not stocking Naloxone

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES