ULSCs is under clinical development by RESTEM and currently in Phase I for Gastrointestinal Bleeding (Gastrointestinal Hemorrhage). According to GlobalData, Phase I drugs for Gastrointestinal Bleeding (Gastrointestinal Hemorrhage) have a 75% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ULSCs’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.
ULSCs overview
The therapeutic candidate is under development for the treatment of coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), idiopathic inflammatory myositis including dermatomyositis and polymyositis duchenne, muscular dystrophy in chindren and to prevent left ventricular assist device (LVAD) associated angiodysplastic bleeding. The drug candidate comprises of umbilical cord lining mesenchymal stem cells (ULSCs). It is administered through intravenous route.
RESTEM overview
RESTEM is discovering and developing cell therapeutics for immune system. The company is headquartered in Corona, California, the US.
For a complete picture of ULSCs’s drug-specific PTSR and LoA scores, buy the report here.
Data Insights
From
The gold standard of business intelligence.
Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.
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.
