AstraZeneca and Merck win new approval for Lynparza in the USA
London-listed AstraZeneca (LSE: AZN) and its development partner Merck & Co (NYSE: MRK) have announced another US Food and Drug Administration approval for the leading PARP blocker Lynparza (olaparib).
The US regulator has approved the therapy for the maintenance treatment of certain adults with advanced epithelial ovarian, fallopian tube or primary peritoneal cancer.
The approval was based on positive results from the Phase III SOLO-1 trial, in which Lynparza reduced the risk of disease progression or death by 70% compared to placebo.
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