Denosumab biosimilar is under clinical development by Fresenius Kabi SwissBioSim and currently in Pre-Registration for Glucocorticoid-Induced Osteoporosis. According to GlobalData, Pre-Registration drugs for Glucocorticoid-Induced Osteoporosis does not have sufficient historical data to build an indication benchmark PTSR for Pre-Registration. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Denosumab biosimilar LoA Report. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Denosumab biosimilar overview
Denosumab biosimilar (FKS518) is under development for the treatment of post menopausal osteoporosis, glucocorticoid-induced osteoporosis, to increase bone mass in men and women at high risk for fracture, increase bone mass in men with osteoporosis, prevention of skeletal-related events in cancer patients, adults and skeletally mature adolescents with giant cell tumor of bone and hypercalcemia. It is administered through subcutaneous route as solution. The therapeutic candidate is a monoclonal antibody acts by targeting receptor activator of nuclear factor kappa B ligand (RANKL).
Fresenius Kabi SwissBioSim overview
Fresenius Kabi SwissBioSim, a subsidiary of Fresenius Kabi AG, is a biopharmaceutical company that develops novel therapeutics for treating autoimmune disease and oncology. The company is headquartered in Eysins, Waadt, Switzerland.
For a complete picture of Denosumab biosimilar’s drug-specific PTSR and LoA scores, buy the report here.
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