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.
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