This is a match-making section for JPIAMR 14th call - Disrupting drug Resistance Using Innovative Design (DRUID).
Human Health
preclinical and clinical studies in human and in all veterinary settings
anti-virulence;small molecule; potentiation of antibiotic efficacy; MRSA;biofilm inhibition
Q2Pharma is looking for partners with expertise in medicinal chemistry, animal experiments, regulatory expertise, toxicity trials
F19 is a small-molecule drug that disarms the pathogen of disease-causing toxins. It binds to a staphylococcal transcription factor, thereby preventing its association with DNA. The result is blockage of transcription of a series of toxins. Efficacy has been established against MRSA, Staph epidermidis, Streptococcus pyogens and Streptococcus pneumoniae. F19 is developed for oral, parenteral and topical application. We are about half way through the preclinical stage. In vivo efficacy and toxicity data are available, as well as PK data. In addition to toxin inhibition F19 also potentiates the efficacy of conventional antibiotics in combination therapy. This property allows the reintroduction of obsolete antibiotics into the clinic. Additionally, F19 inhibits biofilm formation.
Submitted on 2022-02-02 10:56:36
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