Gen1E-1124 is under clinical development by GEn1E Lifesciences and currently in Phase I for Coronavirus Disease 2019 (COVID-19) Associated Acute Respiratory Distress Syndrome. According to GlobalData, Phase I drugs for Coronavirus Disease 2019 (COVID-19) Associated Acute Respiratory Distress Syndrome have a 90% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Gen1E-1124’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.
Gen1E-1124 overview
Gen1E-1124 is under development for the treatment of acute respiratory distress syndrome (ARDS), influenza induced pneumonia. The drug candidates act by targeting mitogen activated protein kinase 14 (MAP Kinase p38 Alpha). It is administered through intravenous route.
Gen1E-1124 was under development for the treatment of acute lung injury (ALI), COVID-19 pneumonia and unspecified renal disease (nephrology).
GEn1E Lifesciences overview
GEn1E Lifesciences is biotechnology company which is engaged in the research and development of immunomodulatory therapies for rare & inflammatory diseases. It is headquartered in Palo Alto, California, the US.
For a complete picture of Gen1E-1124’s drug-specific PTSR and LoA scores, buy the report here.
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