EXIT COVID-19 has initiated enrollment of 75 COVID-19 patients with moderate-to-severe ARDS at multiple research sites across the U.S. The primary efficacy endpoints will be all-cause mortality and median days to recovery.
Chief Medical Officer Vik Sengupta, MD, states, “We have pursued a relentless path since April 2020 when the 24 inpatients were treated, and ExoFlo’s potential as a therapeutic countermeasure against severe COVID-19 first became clear. Patients in the U.S. deserve safe, innovative therapies that meet the highest standards of value and evidence-based medicine, and our phase II double-blind, placebo-controlled, randomized clinical trial is the next step in that process. It will continue to be my priority to maintain these standards as we investigate the potential benefit of ExoFlo as a treatment for COVID-19 associated ARDS.”
“This signifies an important milestone in the progression of our product platform development to help in the fight against COVID-19,” states Joe Schmidt, Co-Founder and President. “This novel therapy has the potential both to improve outcomes for patients and also to reduce overall costs of hospital stays and adjunctive treatments by speeding recovery and reducing the need or length of ICU time.”
Mark Adams, Co-Founder and Chief Executive Officer, states, “We are excited to start enrolling patients in the study and look forward to seeing the outcomes of this advanced therapy. We are dedicated to bringing to market a novel treatment at an accelerated pace to help patients suffering from this devastating disease.”