PTG-007 is under clinical development by PolTREG and currently in Phase II for Type 1 Diabetes (Juvenile Diabetes). According to GlobalData, Phase II drugs for Type 1 Diabetes (Juvenile Diabetes) have a 53% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how PTG-007’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.
PTG-007 overview
PTG-007 is under development for the treatment of type 1 diabetes in children and relapsing remitting multiple sclerosis, primary progressive multiple sclerosis, amyotrophic lateral sclerosis. It comprises of T-regulatory autologous lymphocytes. It is administered through intravenous route and intrathecal route.
PolTREG overview
PolTREG is a provider of biotechnology research and development services that develops therapies for autoimmune diseases using T-regulatory cells.It is headquartered in Gdansk, Poland.
For a complete picture of PTG-007’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.
