TEDA-9 is under clinical development by S.Biomedics and currently in Phase II for Parkinson’s Disease. According to GlobalData, Phase II drugs for Parkinson’s Disease have a 41% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how TEDA-9’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
TEDA-9 overview
TEDA-9 is under development for the treatment of Parkinson's disease. Cell therapy comprises of A9 dopaminergic neuron precursor cells derived from embryonic stem cells. The therapeutic candidate is being developed based on targeted embryonic stem cell differentiation (TED) technology. It is administered through parenteral route.
S.Biomedics overview
S.Biomedics specialized in the field of stem cell therapy. It is headquartered in Seongdong, Seoul, South Korea.
For a complete picture of TEDA-9’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.
