CTS-2016 is under clinical development by CytosinLab Therapeutics and currently in Phase I for Refractory Acute Myeloid Leukemia. According to GlobalData, Phase I drugs for Refractory Acute Myeloid Leukemia have a 68% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CTS-2016’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.
CTS-2016 overview
CTS-2016 is under development for the treatment of relapsed and refractory acute myeloid leukemia (AML), intermediate-to-high risk myelodysplastic syndrome (MDS) and solid tumors including non-small cell lung cancer, triple-negative breast cancer. It is administered by oral route as capsule. The drug candidate acts by targeting AXL and FLT3.
CytosinLab Therapeutics overview
CytosinLab Therapeutics (CytosinLab) is focuses on the field of epigenetics and the development of new drugs that used to accelerate the development of multiple epigenetic targeted new drugs on the Sailan Pharmaceutical pipeline to the clinic. CytosinLab is headquartered in Shanghai, China.
For a complete picture of CTS-2016’s drug-specific PTSR and LoA scores, buy the report here.
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