BiomX announces the Company will present data from BiomX’s Phase 1b/2a study of BX004 for the treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa pulmonary infections. The poster, titled “Novel nebulized phage cocktail in CF patients with chronic P. aeruginosa pulmonary infection: a Ph1b/2a randomized, double-blind, placebo-controlled trial,” reports that the Company’s phage cocktail, BX004-A, demonstrated favorable safety and notable microbiologic and clinical efficacy in cystic fibrosis patients with chronic P. aeruginosa pulmonary infections, including in patients on standard of care treatment of elexacaftor / tezacaftor / ivacaftor or ETI . The poster will be available on the Company’s website following the poster session. “These data, which encapsulate our previously announced Phase 1b/2a study, continue to be encouraging and support our novel approach to treating cystic fibrosis. The European Respiratory Society is an important opportunity to share these results with the European scientific community, and we are grateful to share these positive data,” commented Jonathan Solomon, BiomX Chief Executive Officer.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on PHGE:
- UPDATE ON UNITS – BiomX Inc. Announces 1-for-10 Reverse Stock Split
- BiomX announces 1-for-10 reverse stock split
- BiomX Inc. Announces 1-for-10 Reverse Stock Split
- BiomX Reports Second Quarter 2024 Financial Results and Provides Business and Program Updates
- BiomX to Host Second Quarter 2024 Financial Results Conference Call and Webcast on August 15, 2024