Denosumab biosimilar is under clinical development by Sandoz Group and currently in Pre-Registration for Humoral Hypercalcemia of Malignancy. According to GlobalData, Pre-Registration drugs for Humoral Hypercalcemia of Malignancy have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how Denosumab biosimilar’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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 (GP-2411) is under development for the treatment of postmenopausal osteoporosis, treatment-induced bone loss, metastases to bone, giant cell tumor of bone. It is administered through subcutaneous route as an injection. The drug candidate acts by targeting the receptor activator of nuclear factor kappa B ligand (RANKL).
Sandoz Group overview
Sandoz Group develops, manufactures and distributes generics and biosimilar medical products used for the treatment of various life threatening diseases. The company is headquartered in Zug City, Zug, Switzerland.
For a complete picture of Denosumab biosimilar’s drug-specific PTSR and LoA scores, buy the report here.
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