MER-3101 is under clinical development by Mercia Pharma and currently in Phase I for Type 1 Diabetes (Juvenile Diabetes). According to GlobalData, Phase I drugs for Type 1 Diabetes (Juvenile Diabetes) have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how MER-3101’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.

MER-3101 overview

MER-3101 is under development for the prevention and treatment of type 1 diabetes. The drug candidate is a vaccine comprises of insulin B-chain which is administered with MAS-1, a nanoparticle, emulsion-based adjuvant. It is developed based on MERIT (MERcia immunotherapeutic) technology, which pushes the immune system to restore self-tolerance to specific antigens (autoimmunity). Vaccine  candidate is administered through intramuscular route as emulsion.

For a complete picture of MER-3101’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 16 July 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.