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Study With Phage for CF Subjects With Pseudomonas Lung Infection
A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate Nebulized Bacteriophage Treatment in Outpatient Adult Cystic Fibrosis (CF) Subjects With Chronic Pseudomonas Aeruginosa (PsA) Pulmonary Infection
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Key Inclusion Criteria: * Cystic fibrosis patients with chronic Pseudomonas aeruginosa pulmonary infection receiving standard of care inhaled antibiotics (cycling or continuous regimen) or no inhaled antibiotics * Age ≥ 18 years * FEV1 40%-80% predicted * Clinically stable lung disease * Willing and able to provide adequate sputum samples, using any method (spontaneously expectorated, induced, from home or clinic) at designated study visits. Key Exclusion Criteria: * Known hypersensitivity to bacteriophages or excipients in the formulation. * Receipt of prior bacteriophage therapy within the 6 months prior to Screening or Day 1 * Detection of Burkholderia cenocepacia from respiratory tract within 1 year prior to Screening or from Screening culture * Currently receiving systemic treatment for allergic bronchopulmonary aspergillosis * Currently receiving treatment for active infection with non-tuberculous mycobacteria or prior detection of Mycobacterium abscessus in 12 months prior to Screening * History of severe neutropenia * History of lung transplant * History of solid organ transplant * Acquired or primary immunodeficiency syndrome * Initiation or change in type of CFTR modulator less than 3 months prior to Screening * Pregnant or breastfeeding female
About the study
The goal of this Phase 2b clinical trial is to see if nebulized phage (BX004) can treat chronic Pseudomonas aeruginosa (PsA) lung infection in CF subjects. The primary goal is to see if 8 weeks of twice daily BX004 can reduce the amount of PsA in the sputum compared to placebo (on top of background CF therapy).
What is being tested
- BX004 (biological)
- Placebo (other)
Sponsor: BiomX Ltd · Participants: 63 · Started: Jul 2, 2025
Contact the study team
- Urania Rappo, MD · Phone: 1-617-256-2625
Official record on ClinicalTrials.gov — NCT06998043
Locations in the U.S.
| Alabama | University of Alabama at Birmingham, Birmingham |
| Alaska | Providence Alaska Medical Center, Anchorage (Not yet recruiting) |
| Arkansas | University of Arkansas for Medical Sciences, Little Rock (Not yet recruiting) |
| California | Stanford University, Palo Alto (Not yet recruiting) University of California San Francisco, San Francisco |
| Colorado | National Jewish Health, Denver |
| Florida | Joe DiMaggio Children's Health, Hollywood (Not yet recruiting) Central Florida Pulmonary Group, Orlando Avanza Medical Center, Pensacola |
| New Jersey | Rutgers, Robert Wood Johnson Medical School, New Brunswick |
| New York | New York Medical College, Hawthorne Northwell Health, New York |
| Tennessee | Vanderbilt University Medical Center, Nashville |
| Utah | University of Utah, Salt Lake City (Not yet recruiting) |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.