INM-004 is under clinical development by Inmunova and currently in Phase III for Typical Hemolytic Uremic Syndrome (Shiga-Toxin Associated Hemolytic Uremic Syndrome). According to GlobalData, Phase III drugs for Typical Hemolytic Uremic Syndrome (Shiga-Toxin Associated Hemolytic Uremic Syndrome) 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 INM-004 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.
INM-004 overview
INM-004 was under development for the treatment of hemolytic uremic syndrome (HUS) associated to Shigatoxin producing Escherichia coli (STEC). The drug candidate is an neutralizing equine anti shiga-toxin hyperimmune immunoglobulin F(ab')2 fragment. It is administered by intravenous route as a solution. The drug candidate is developed based on IMC platform technology which uses the enzyme lumazine synthase of Brucella species.
For a complete picture of INM-004’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.
