Hygromycin is under clinical development by Flightpath BioSciences and currently in Phase I for Lyme Disease. According to GlobalData, Phase I drugs for Lyme Disease have a 75% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Hygromycin’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.
Hygromycin overview
Hygromycin (FP-100) is under development for the treatment of acute lyme borreliosis, endemic treponematoses (yaws), colorectal cancer, oral squamous cell carcinoma and syphilis. It is administered through oral route. It acts by targeting bacterial ribosomal peptidyl transferase.
It was also under treatment for periodontal disease and Weil's disease.
Flightpath BioSciences overview
Flightpath BioSciences is a developer of antibiotic therapies designed to treat pathogen-driven diseases. It kills infectious bacteria in lyme disease and offers antibiotic therapies to reduce the negative impact on the microbiome. The company is headquartered in Berkeley, California, the US.
For a complete picture of Hygromycin’s drug-specific PTSR and LoA scores, buy the report here.
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