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Ondine Biomedical completes patient recruitment for US Phase II nasal photodisinfection trial | ||
By: PR Newswire Association LLC. - 08 Aug 2022 | Back to overview list |
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VANCOUVER, BC, Aug. 8, 2022 /PRNewswire/ -- Ondine Biomedical Inc. (LON: OBI), has recruited the final patient to its nasal photodisinfection exploratory Phase 2 trial. The trial is evaluating how effectively Ondine's nasal photodisinfection technology eradicates pathogens – specifically Staphylococcus aureus - in the nose. The single-center, BENEFIT-aPDT open-label study is being carried out at HCA Healthcare's Memorial Health University Medical Center in Savannah, Georgia, and has recruited over 300 patients. Recruited patients undergo a pre-surgery nasal culture to determine the prevalence of Staphylococcus aureus, the main cause of surgical site infections. Each patient then receives Ondine's nasal photodisinfection (investigational product) followed by a post-treatment culture, enabling evaluation of the efficacy of nasal photodisinfection across a wide range of patients and surgery types. Carolyn Cross, Ondine's CEO commented "Completing patient recruitment on this Phase II trial is an important step in our clinical development, and we look forward to being able to share the trial results in due course. We appreciate HCA's support throughout the trial, and their focus on the importance of reducing SSIs. Ours is a truly novel approach to nasal disinfection, and we believe that our technology has the potential to have a significant effect on combatting SSIs, complications, and extended hospital stays." SSIs are the leading cause of readmissions to hospital following surgery and a significant cause of post-surgical morbidity and mortality, with approximately 3% of patients who contract an SSI dying as a consequence. Post-operative infections occur in up to 300,000 patients per year in the United States and cost the US healthcare system tens of billions of dollars a year[i]. About Ondine Biomedical Inc. Ondine's technology is approved in a number of jurisdictions and has been awarded the CE mark, as well as Qualified Infectious Disease Product and Fast Track status in the US by the FDA. [i] https://www.sciencedaily.com/releases/2017/01/170119161551.htm |
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