StroMel is under clinical development by Akan Biosciences and currently in Phase II for Osteoarthritis. According to GlobalData, Phase II drugs for Osteoarthritis have a 45% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how StroMel’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.
StroMel overview
StroMel is under development for the treatment of knee osteoarthritis, hip and shoulder osteoarthritis, wound healing and autism in children. The drug candidate comprises of autologous mesenchymal stem cells (MSC). It is administered through intraarticular route.
Akan Biosciences overview
Akan Biosciences is developing regenerative medical products to treat injuries and inflammatory diseases. The company is headquartered in Gaithersburg, Maryland, the US.
For a complete picture of StroMel’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.
