Aridis Pharmaceuticals (NASDAQ:ARDS) enrolls first COVID-19 patient in its ongoing Phase 3 clinical trial of AR-301, a monoclonal antibody against S. aureus-induced pneumonia in patients who were already on mechanical ventilators.
COVID-19 patients on prolonged mechanical
ventilation are prone to secondary infections (also called
‘superinfections’) by opportunistic pathogens such as bacteria.
Superinfection is a reported complication in COVID-19 patients which exacerbates morbidity and rate of mortality.
“While AR-301 does not treat the virus that causes
COVID-19 disease, it can potentially mitigate secondary S. aureus
bacterial pneumonia, which represents a serious coronavirus complication
and a cause of death in such patients,” says Vu Truong, CEO.
The study is expected to enroll 240 patients.
https://seekingalpha.com/news/3568101-aridis-pharm-enrolls-first-covidminus-19-patient-in-late-stage-arminus-301-trial
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