Some eight months after gaining marketing clearance for the drug in the USA, and an April advisory committee recommendation in Europe, US pharma giant Pfizer (NYSE: PFE) has now also won approval for Talzenna (talazoparib) in the European Union.
The company announced on Friday that the European Commission approved Talzenna, an oral poly (ADP-ribose) polymerase (PARP) inhibitor,as monotherapy for the treatment of adult patients with germline breast cancer susceptibility gene (gBRCA)1/2-mutations, who have human epidermal growth factor receptor 2-negative (HER2-) locally advanced (LA) or metastatic breast cancer (MBC).
Means $15 million milestone for BioMarin
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