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Clinical Trial
of TRIOFAG®

TRIOFAG® offers an innovative biological solution for the targeted treatment of bacterial respiratory infections. Developed by FAGOFARMA, this product contains carefully selected bacteriophages that attack and eliminate three key pathogens: Acinetobacter baumannii, Klebsiella pneumoniae, and Staphylococcus aureus.

Unlike conventional antibiotics, bacteriophages act with exceptional selectivity — they do not affect human cells or the natural microbiota, providing a gentler and more effective therapeutic approach. TRIOFAG® represents a new generation of therapy at a time when antibacterial resistance is one of the most pressing global health challenges.

The TRIOFAG® project is conducted in full compliance with Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) standards. Entering clinical trials marks a significant step forward in FAGOFARMA’s commitment to bringing bacteriophage therapy from research into clinical practice — precisely where it is needed most.

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PROJECT TIMELINE

  • December 2022: Design of the TRIOFAG® phage cocktail

  • February 2024: Scientific advice received from the State Institute for Drug Control

  • February 2025: Repeated-dose oral toxicity study (GLP) demonstrates that TRIOFAG® is well tolerated and shows no adverse effects in Wistar rats

  • July 2025: First draft of the clinical trial protocol synopsis completed

  • March 2026: Planned application for clinical trial 

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FOR INVESTORS

Become part of the innovation in respiratory infection treatment.

FAGOFARMA offers an opportunity to invest in the clinical development of TRIOFAG®, a new generation of targeted bacteriophage therapy.

For more information, please do not hesitate to contact us

FAGOFARMA s.r.o.

Londýnská 730/59

120 00 Praha 2, Czech Republic

www.fagofarma.cz

© 2022 FAGOFARMA s.r.o

Created by levvel.cz

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