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Amgen and UCB Resubmit BLA for Evenity to the FDA for the Treatment of Osteoporosis

09:46 EDT 13 Jul 2018 | Speciality Pharma Journal

THOUSAND OAKS, Calif. and BRUSSELS, July 12, 2018 /PRNewswire/ — Amgen (NASDAQ:AMGN) and UCB (Euronext Brussels: UCB) today announced the resubmission of the Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for EVENITY™* (romosozumab), an investigational monoclonal antibody for the treatment of osteoporosis in postmenopausal women at high risk for fracture. EVENITY increases bone formation and reduces bone resorption …

Original Article: Amgen and UCB Resubmit BLA for Evenity to the FDA for the Treatment of Osteoporosis

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