Progerinin is under clinical development by PRG S&Tech and currently in Phase I for Hutchinson-Gilford Progeria. According to GlobalData, Phase I drugs for Hutchinson-Gilford Progeria does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Progerinin 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.

Progerinin overview

Progerinin (PRGS-1) is under development for the treatment of Hutchinson-Gilford progeria and Werner syndrome. It is administered through oral route.

PRG S&Tech overview

PRG S&Tech specializes in the research and development of medicine for genopathies diseases. PRG S&Tech is headquartered in Busan,South Korea.

For a complete picture of Progerinin’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.