Commercial prospects for the six-month-old global collaboration between AstraZeneca PLC and Merck & Co. Inc. to jointly develop and commercialize AZ's Lynparza (olaparib) got a big boost Jan. 12 when the FDA expanded use of the PARP inhibitor to include treatment of patients with metastatic breast cancer who have a mutated BRCA gene, the first such regulatory approval globally.
Lynparza Gets First Mover Advantage In BRCA-Positive Breast Cancer
AstraZeneca and Merck & Co hope to advance Lynparza quickly in prostate and pancreatic cancers after getting first mover advantage in metastatic breast cancer.

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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
By allowing it to enter the brain more easily, trontinemab’s brain shuttle brings more patients to ‘amyloid zero’ levels faster, and with fewer brain swelling side effects.
Compass' bispecific antibody tovecimig hits primary efficacy endpoint in Phase II/III top-line data in advanced biliary tract cancer, and may have class side-effect advantages. But additional survival data may be needed to support US approval.