177Lutetium-miltuximab is under clinical development by GlyTherix and currently in Phase I for Urethral Cancer. According to GlobalData, Phase I drugs for Urethral Cancer does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the 177Lutetium-miltuximab 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.
177Lutetium-miltuximab overview
Miltuximab is under development for the treatment of metastatic prostate cancer, metastatic pancreatic cancer, metastatic urothelial cancer, bladder cancer, ureter cancer, urethral cancer, glioblastoma, breast cancer, ovarian cancer and esophageal cancer. It is administered through intravenous route. The drug is a radionuclide drug conjugate (RDC) which contains glypican 1 (GPC1) labelled with lutetium-177 (177Lu) radionuclide.
GlyTherix overview
GlyTherix, is a biotech company that specialises in immuno oncology therapeutics for solid tumors, targeted treatment of prostate, bladder and pancreas cancers. The company is headquartered in Macquarie Park, New South Wales, Australia.
For a complete picture of 177Lutetium-miltuximab’s drug-specific PTSR and LoA scores, buy the report here.
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