Cyclosam is under clinical development by Telix Pharmaceuticals and currently in Phase I for Metastatic Breast Cancer. According to GlobalData, Phase I drugs for Metastatic Breast Cancer have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Cyclosam’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.

Cyclosam overview

Cyclosam is under development for the treatment of osteosarcoma, Ewing sarcoma, bone metastasis and metastatic prostate, breast, and lung cancer which is metastatic to bone. The therapeutic candidate is a radiopharmaceutical comprising samarium-153 DOTMP. It is administered through parenteral route.

Telix Pharmaceuticals overview

Telix Pharmaceuticals (Telix) is a commercial-stage biopharmaceutical company that develops and commercializes therapeutic and diagnostic radiopharmaceuticals. It utilizes targeted radiation technology to target small molecule or antibody that binds to tumor cells. The company’s pipeline products include TLX592, TLX591-CDx and TLX591 radio antibody-drug conjugate (rADC) directed at PSMA that targets prostate cancer; TLX250-CDx and TLX250 for kidney cancer; TLX101-CDx and TLX101 treat brain cancer; TLX66-CDx and TLX66 for bone marrow conditioning; and TLX300 and TLX300-CDx. It offers Illuccix, an imaging agent targeting men with prostate cancer. Telix’s brands include RADmAb, Zircaix, Scintimun and Pixclara. The company operates its offices in Japan, Australia, Canada, the US and Switzerland. Telix is headquartered in North Melbourne, Victoria, Australia.

For a complete picture of Cyclosam’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.