CTO-1681 is under clinical development by CytoAgents and currently in Phase II for Cytokine Release Syndrome (Cytokine Storm). According to GlobalData, Phase II drugs for Cytokine Release Syndrome (Cytokine Storm) have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how CTO-1681’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.
CTO-1681 overview
CTO-1681 is under development for the treatment of influenza A virus subtype H5N1 and H1N1 infections, COVID-19 associated cytokine release syndrome (cytokine storm) and cytokine release syndrome in oncology. The drug candidate is a small molecule, it is administered orally. It is a beraprost isomer (isomer A), which acts by targeting G-protein coupled receptor (GPCR) and nuclear factor kappa B (NF-kB). It was under development for the treatment of COVID-19 disease.
CytoAgents overview
CytoAgents is a biotechnology company that engaged in the development of innovative pharmaceutical products. The company is headquartered in United States.
For a complete picture of CTO-1681’s drug-specific PTSR and LoA scores, buy the report here.
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