IMM-124E is under clinical development by Immuron and currently in Phase II for Traveler’s Diarrhea. According to GlobalData, Phase II drugs for Traveler’s Diarrhea have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how IMM-124E’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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IMM-124E overview
IMM-124E is under development for the treatment of non alcoholic fatty liver disease (NAFLD) colitis, type II diabetes, urinary tract infections, shigella infections, Traveler's diarrhea, autism and coronavirus disease 2019 caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is administered orally. IMM-124E is a formulation of hyper-immune bovine colostrum powder (BCP). The drug candidate targets Lipopolysaccharide (LPS). The drug candidate is based on dairy derived polyclonal antibody platform.
The drug candidate was under development for alcoholic steatohepatitis (ASH) and non-alcoholic steatohepatitis (NASH).
Immuron overview
Immuron, formerly Anadis, is a biopharmaceutical company that develops oral immunotherapy therapeutics using polyclonal antibody products for humans. The company develops and produces an orally stable therapeutic for various immune mediated and inflammatory disorders. It provides products such as travelan, proctectyn, IMM 124E and IMM 529. Immuron’s travelan is a natural product designed to prevent infection by enterotoxigenic Escherichia coli. The company develops unique oral immunotherapy platform improving the immunological balance by orally administered safe compounds. The company produces therapeutics for non-alcoholic steatohepatitis (NASH) diabetes, alcoholic steatohepatits, colitis, arthritis, inflammatory bowel diseases, irritable bowel syndrome, liver fibrosis and other chronic disorders. Immuron is headquartered in Melbourne, Victoria, Australia.
For a complete picture of IMM-124E’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.
