Vartocell is under clinical development by Cell Tech Pharmed and currently in Phase III for Spastic Cerebral Palsy. According to GlobalData, Phase III drugs for Spastic Cerebral Palsy does not have sufficient historical data to build an indication benchmark PTSR for Phase III. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Vartocell LoA Report. 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.

Vartocell overview

Vartocell is under development for the treatment of acute myocardial infarction induced heart failure and pediatric spastic cerebral palsy. The therapy comprises of allogeneic live umbilical cord-derived mesenchymal stem cells. It is administered through intrathecal and Intracoronary routes. It was under development for the treatment of spinal muscular atrophy type I, II and III.

For a complete picture of Vartocell’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.