AstraZeneca (LSE: AZN) has entered into a definitive agreement with Foundation Medicine to develop a novel companion diagnostic assay for its cancer drug Lynparza (olaparib) to support its global development program.
The companion diagnostic will enable physicians to identify those patients most likely to benefit from Anglo-Swedish pharma major AstraZeneca’s first-in-class poly ADP-ribose polymerase (PARP) inhibitor.
Lynparza is an innovative, oral PARP inhibitor that exploits tumor DNA repair pathway deficiencies to preferentially kill cancer cells. This mode of action gives Lynparza the potential for activity in a range of tumor types with DNA repair deficiencies. It is approved in the USA for the treatment of patients with germline BRCA-mutated advanced ovarian cancer and in the EU for patients with platinum-sensitive relapsed BRCA-mutated high-grade serous epithelial ovarian, fallopian tube or primary peritoneal cancer.
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