Radspherin is under clinical development by Oncoinvent and currently in Phase II for Fallopian Tube Cancer. According to GlobalData, Phase II drugs for Fallopian Tube Cancer have a 41% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Radspherin’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
Radspherin overview
Radspherin is under development for the treatment of metastatic cancers including peritoneal carcinomatosis originating from ovarian cancer, fallopian cancer, peritoneal cancer and colorectal cancer. The drug is a radionuclide drug conjugate (RDC) which contains a monoclonal antibody OI-3 conjugated to a radioisotope. The drug candidate is a suspension of inorganic alpha-emitting radioactive microspheres and administered as intraperitoneal injection. It acts by targeting CD146 antigen.
Oncoinvent overview
Oncoinvent is a pharmaceutical company that develops innovative products aimed at improving treatment options for cancer patients. The company’s lead product candidate is Radspherin, an alpha-emitting radioactive microparticle suspension designed for local treatment of metastatic cancers in body cavities. Oncoinvent product is primarily targeted towards patients suffering from peritoneal carcinomatosis (PC). It also operates a Good Manufacturing Practice (GMP) standard production and lab facility for radiopharmaceuticals, which is capable of supplying Radspherin for large multi-center clinical studies. Oncoinvent is headquartered in Oslo, Norway.
For a complete picture of Radspherin’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
