Friomaramide, a Novel Hexapeptide, Inhibits Liver Stage Plasmodium Falciparum

Tech ID: 18B168

Competitive Advantages

  • A novel molecule that can inhibit P. falciparum in malaria
  • Bypasses drug resistance
  • Limited toxicity towards human cells

Summary

USF researchers have developed a novel modified hexapeptide called friomaramide. It inhibits the growth of P. falciparum to a similar degree as the antimalarial drug primaquine, with the added benefit of bypassing growing antimalarial resistance. It is also less toxic to human cells. Friomaramide may prove to be a huge benefit to the millions of people infected with malaria worldwide every year. 

Friomaramide Showing Comparable Inhibition of P. falciparum as Prinaquine

Desired Partnerships

  • License
  • Sponsored Research
  • Co-Development

 

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