AstraZeneca/Merck's Lynparza Combo Ovarian Cancer Study Fails

 | Mar 13, 2020 04:11AM ET

AstraZeneca plc (NYSE:AZN) and partner Merck (NYSE:MRK) announced that a phase III study evaluating a combination regimen of their successful PARP inhibitor, Lynparza in patients with platinum-sensitive relapsed ovarian cancer failed to meet the primary endpoint

The GY004 study was led by NRG Oncology and sponsored by the U.S. National Cancer Institute (NCI) and evaluated the safety and efficacy of a potential new medicine cediranib added to Lynparza versus platinum-based chemotherapy in the above patient population.

The study failed to show a statistically significant improvement in progression-free survival (PFS) with cediranib (an oral VEGF receptor inhibitor) added to Lynparza in the intent-to-treat (ITT) population, thereby not meeting the primary endpoint

Shares of AstraZeneca and Merck declined 8.6% and 6.1%, respectively on Thursday in response to the news and also due to coronavirus related market sell-off. In the past year, shares of AstraZeneca and Merck have declined 18.3% and 18.2%, respectively compared with the industry ’s decrease of 9.9%.