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Il portafoglio oncologico di Novartis, a pochi giorni dall'acquisizione di AAA, si rafforza ulteriormente. Il gigante farmaceutico basilese ha annunciato che la sua neo acquisita Advanced Accelerator Applications ha ricevuto il via libera da parte della Food and Drug Administration (FDA) statunitense per il Lutathera per il trattamento dei tumori neuroendocrini gastroenteropancreatici positivi, inclusi i tumori neuroendocrini negli adulti.
Il farmaco in questione, che ha ricevuto il nulla osta della FDA è un medicinale di punta e il primo "Peptide Receptor Receptor Recognition Therapy" approvato dall'ente statunitense. Si tratta di una forma di trattamento che comprende una molecola mirata che trasporta un componente radioattivo.
ATS/Swing
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