The need for Bayer AG/Algeta ASA’s prostate cancer radiotherapeutic Xofigo (radium Ra 223 dichloride) to be administered at a licensed site could pose access issues that could impact the speed of the launch.
FDA approved Xofigo May 15 for the treatment of castration-resistant prostate cancer in patients with symptomatic bone metastases, a critically ill subset that gives Bayer and Algeta a more specific target than Johnson & Johnson’s Zytiga (abiraterone acetate) and