J&J granted marketing authorization for Akeega in Europe
The Fly

J&J granted marketing authorization for Akeega in Europe

Johnson & Johnson’s Janssen Pharmaceutical announced that the European Commission has granted marketing authorization for Akeega in the form of a dual action tablet, given with prednisone or prednisolone, for the treatment of adults with metastatic castration-resistant prostate cancer and BRCA1/2 mutations in whom chemotherapy is not clinically indicated.

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