COYA-301 is under clinical development by Coya Therapeutics and currently in Phase II for Alzheimer’s Disease. According to GlobalData, Phase II drugs for Alzheimer’s Disease have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how COYA-301’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.
COYA-301 overview
COYA-301 is under development for the treatment of Alzheimer's disease (AD). It comprises of comprises low dose recombinant human interleukin 2 and is administered through subcutaneous route. The therapeutic candidate acts by targeting IL-2 receptor.
It was also under development for frontotemporal dementia (FTD).
Coya Therapeutics overview
Coya Therapeutics (Coya) is a cellular therapy platform that discovers and develops therapeutics for the treatment of neurodegenerative and autoimmune diseases. Coya is headquartered in Houston, Texas, the US.
For a complete picture of COYA-301’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.
