Mesenchymal Stem Cells-Derived Exosomes is under clinical development by Cellular Biomedicine Group and currently in Phase II for Dermatomyositis. According to GlobalData, Phase II drugs for Dermatomyositis have a 60% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Mesenchymal Stem Cells-Derived Exosomes’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.
Mesenchymal Stem Cells-Derived Exosomes overview
The drug candidate is under development for the treatment of moderate to severe acute respiratory distress syndrome, pneumonia caused by beta-coronavirus(SARS-CoV-2 or Covid-19) and dementia due to Alzheimer's disease. It is administered through inhalation route as an aerosol and as intravenous bolus. The drug candidate comprises of exosomes derived from allogenic adipose mesenchymal stem cells(MSCs-Exo).
For a complete picture of Mesenchymal Stem Cells-Derived Exosomes’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.
