medical conditions 9. have spo2 ≤ 93% on room air, respiratory rate ≥30 per minute, resting heart rate ≥125 per minute. 10. require mechanical ventilation or anticipated impending need for mechanical ventilation 11. have known allergies to any of the components used in the formulation of the interventions. 12. have hemodynamic instability requiring use of pressors within 24 hours of randomization. 13. suspected or proven serious, active bacterial, fungal, viral, or other infection (besides covid-19) that in the opinion of the investigator could constitute a risk when taking intervention. 14. have any co-morbidity requiring surgery or that is considered life- threatening within 29 days prior to dosing. 15. have any serious concomitant systemic disease, condition or disorder that, in the opinion of the investigator, should preclude participation in this study. other exclusions 16. have a history of a positive sars-cov-2 test prior to the one serving as eligibility for this study. 17. have received an investigational intervention for sars-cov-2 prophylaxis within 30 days before dosing. 18. have received treatment with a sars-cov-2 specific monoclonal antibody. 19. have participated, within the last 30 days, in a clinical study involving an investigational intervention. if the previous investigational intervention has a long half-life, 5 half-lives or 30 days, whichever is longer, should have passed. 20. are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study. 21. are pregnant or breast feeding. 22. are investigator site personnel directly affiliated with this study.

medical conditions 9. have spo2 ≤ 93% on room air, respiratory rate ≥30 per minute, resting heart rate ≥125 per minute. 10. require mechanical ventilation or anticipated impending need for mechanical ventilation 11. have known allergies to any of the components used in the formulation of the interventions. 12. have hemodynamic instability requiring use of pressors within 24 hours of randomization. 13. suspected or proven serious, active bacterial, fungal, viral, or other infection (besides covid-19) that in the opinion of the investigator could constitute a risk when taking intervention. 14. have any co-morbidity requiring surgery or that is considered life- threatening within 29 days prior to dosing. 15. have any serious concomitant systemic disease, condition or disorder that, in the opinion of the investigator, should preclude participation in this study. other exclusions 16. have a history of a positive sars-cov-2 test prior to the one serving as eligibility for this study. 17. have received an investigational intervention for sars-cov-2 prophylaxis within 30 days before dosing. 18. have received treatment with a sars-cov-2 specific monoclonal antibody. 19. have participated, within the last 30 days, in a clinical study involving an investigational intervention. if the previous investigational intervention has a long half-life, 5 half-lives or 30 days, whichever is longer, should have passed. 20. are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study. 21. are pregnant or breast feeding. 22. are investigator site personnel directly affiliated with this study.

medical conditions have spo2 ≤ 93% on room air, respiratory rate ≥30 per minute, resting heart rate ≥125 per minute. require mechanical ventilation or anticipated impending need for mechanical ventilation have known allergies to any of the components used in the formulation of the interventions. have hemodynamic instability requiring use of pressors within 24 hours of randomization. suspected or proven serious, active bacterial, fungal, viral, or other infection (besides covid-19) that in the opinion of the investigator could constitute a risk when taking intervention. have any co-morbidity requiring surgery or that is considered life- threatening within 29 days prior to dosing. have any serious concomitant systemic disease, condition or disorder that, in the opinion of the investigator, should preclude participation in this study. other exclusions have a history of a positive sars-cov-2 test prior to the one serving as eligibility for this study. have received an investigational intervention for sars-cov-2 prophylaxis within 30 days before dosing. have received treatment with a sars-cov-2 specific monoclonal antibody. have participated, within the last 30 days, in a clinical study involving an investigational intervention. if the previous investigational intervention has a long half-life, 5 half-lives or 30 days, whichever is longer, should have passed. are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study. are pregnant or breast feeding. are investigator site personnel directly affiliated with this study.

medical conditions have spo2 ≤ 93% on room air, respiratory rate ≥30 per minute, resting heart rate ≥125 per minute. require mechanical ventilation or anticipated impending need for mechanical ventilation have known allergies to any of the components used in the formulation of the interventions. have hemodynamic instability requiring use of pressors within 24 hours of randomization. suspected or proven serious, active bacterial, fungal, viral, or other infection (besides covid-19) that in the opinion of the investigator could constitute a risk when taking intervention. have any co-morbidity requiring surgery or that is considered life- threatening within 29 days prior to dosing. have any serious concomitant systemic disease, condition or disorder that, in the opinion of the investigator, should preclude participation in this study. other exclusions have a history of a positive sars-cov-2 test prior to the one serving as eligibility for this study. have received an investigational intervention for sars-cov-2 prophylaxis within 30 days before dosing. have received treatment with a sars-cov-2 specific monoclonal antibody. have participated, within the last 30 days, in a clinical study involving an investigational intervention. if the previous investigational intervention has a long half-life, 5 half-lives or 30 days, whichever is longer, should have passed. are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study. are pregnant or breast feeding. are investigator site personnel directly affiliated with this study.