This is a Phase 1 randomized study to evaluate the safety, tolerability and efficacy of IV Ampion in improving the clinical course and outcomes of patients hospitalized with COVID-19 infection who require supplemental oxygen.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
10
Ampion, administered by intravenous infusion
Standard of Care
Research Site
Colorado Springs, Colorado, United States
Incidence and severity of adverse events
Incidence and severity of adverse events
Time frame: Primary endpoint at day 5
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