Biomx Inc. ((PHGE)) announced an update on their ongoing clinical study.
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Study Overview: BiomX Inc. is conducting a Phase 2b clinical trial titled ‘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.’ The study aims to determine if the nebulized phage treatment, BX004, can effectively reduce PsA in the sputum of CF patients over an 8-week period compared to a placebo, alongside standard CF therapy.
Intervention/Treatment: The intervention being tested is a biological treatment known as BX004, a nebulized bacteriophage. This treatment is designed to target and reduce chronic Pseudomonas aeruginosa infections in the lungs of CF patients.
Study Design: This is an interventional study with a randomized allocation and a parallel intervention model. It employs a quadruple masking approach, meaning that the participant, care provider, investigator, and outcomes assessor are all blinded to the treatment allocation. The primary purpose of the study is treatment-focused.
Study Timeline: The study began on May 10, 2025, with the last update submitted on July 17, 2025. These dates are crucial as they indicate the study’s progress and the timeliness of the data being collected.
Market Implications: The ongoing study by BiomX Inc. could significantly impact its stock performance and investor sentiment, especially if the results demonstrate a successful treatment for CF patients. This could position BiomX favorably against competitors in the CF treatment market, potentially leading to increased investor interest and stock value.
The study is currently recruiting, with further details available on the ClinicalTrials portal.