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A Phase 2, Multi-Center, Double-Blind, Randomized, Placebo Controlled Study to Evaluate the Safety, Phage Kinetics, and Efficacy of Inhaled AP-PA02 Multi-Phage Therapeutic in Subjects With Non-Cystic Fibrosis Bronchiectasis and Chronic Pulmonary Pseudomonas Aeruginosa Infection

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Trial Profile

A Phase 2, Multi-Center, Double-Blind, Randomized, Placebo Controlled Study to Evaluate the Safety, Phage Kinetics, and Efficacy of Inhaled AP-PA02 Multi-Phage Therapeutic in Subjects With Non-Cystic Fibrosis Bronchiectasis and Chronic Pulmonary Pseudomonas Aeruginosa Infection

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 25 Dec 2024

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At a glance

  • Drugs AP PA02 (Primary)
  • Indications Bronchiectasis; Pseudomonal infections
  • Focus Therapeutic Use
  • Acronyms Tailwind
  • Sponsors Armata Pharmaceuticals

Most Recent Events

  • 19 Dec 2024 According to an Armata Pharmaceuticals media release, announced encouraging topline results from its Phase 2 ("Tailwind") trial evaluating AP-PA02, a novel, inhaled multi-phage therapeutic for the treatment of chronic pulmonary Pseudomonas aeruginosa infections in non-cystic fibrosis bronchiectasis patients.
  • 19 Dec 2024 Results published in the Armata Pharmaceuticals media release
  • 13 Nov 2024 According to an Armata Pharmaceuticals media release, company remain on-track to report topline data from this study by the end of this year.

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