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MultiStem Administration for COVID-19 Induced ARDS (MACoVIA)
Sponsor: Healios K.K.
Summary
Multicenter investigation featuring an open-label lead-in followed by a double blinded, randomized, placebo-controlled Phase 2/3 part to evaluate the safety and efficacy of MultiStem therapy in subjects with moderate to severe Acute Respiratory Distress Syndrome (ARDS) due to pathogens including COVID-19.
Official title: A Phase 2/3 Study to Assess the Safety and Efficacy of MultiStem® Therapy in Subjects With Acute Respiratory Distress Syndrome (ARDS) Due to Coronavirus Disease (COVID-19)
Key Details
Gender
All
Age Range
18 Years - 89 Years
Study Type
INTERVENTIONAL
Enrollment
22
Start Date
2020-04-28
Completion Date
2024-10-01
Last Updated
2026-10-16
Healthy Volunteers
No
Conditions
Interventions
MultiStem
intravenous infusion
Placebo
intravenous infusion
Locations (4)
Athersys Investigational Site 107
Chicago, Illinois, United States
Athersys Investigational Site 103
Akron, Ohio, United States
Athersys Investigational Site 101
Cleveland, Ohio, United States
Athersys Investigational Site 102
Cleveland, Ohio, United States