VeroXEN is under clinical development by Microgen and currently in Phase I for Tick Borne Encephalitis. According to GlobalData, Phase I drugs for Tick Borne Encephalitis 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 VeroXEN 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.

VeroXEN overview

VeroXEN is under development for the prevention of tick-borne encephalitis. It is administered through intramuscular route in the form of suspension.

Microgen overview

Microgen is a manufacturer of immunobiological products and engaged in production of vaccines for the treatment of infectious diseases. Microgen is headquartered in Moscow, Russia.

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

This content was updated on 10 June 2024

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GlobalData

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.