Do you have any of these conditions: *COVID-19 or Covid-19? |
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Do you have any of these conditions: Covid-19 or *COVID-19? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: *COVID-19 or Covid-19? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: *COVID-19 or Covid-19? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: Covid-19 or *COVID-19? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: *COVID-19 or Covid-19? |
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Is your age greater than or equal to 12 yrs? |
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Is your age greater than or equal to 18 yrs? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: *COVID-19 or Covid-19? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: *COVID-19 or Covid-19? |
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Is your age greater than or equal to 12 yrs? |
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Is your age greater than or equal to 12 yrs? |
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Is your age greater than or equal to 12 yrs? |
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Do you have any of these conditions: Covid-19 or *COVID-19? |
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Gender: Male or Female |
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Are currently not hospitalized |
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Have one or more mild or moderate COVID-19 symptoms: Fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, or shortness of breath with exertion |
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Must have sample taken for test confirming viral infection no more than 3 days prior to starting the drug infusion |
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Are males or non-pregnant females who agree to contraceptive requirements |
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Understand and agree to comply with planned study procedures |
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Agree to the collection of nasopharyngeal swabs and venous blood |
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The participant or legally authorized representative give signed informed consent and/or assent |
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Participants in treatment arms 7 and 8 ONLY |
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Are greater than or equal to ()18 years of age and must satisfy at least one of the following at the time of screening |
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Are 65 years of age |
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Have a body mass index (BMI) 35 |
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Have chronic kidney disease (CKD) |
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Have type 1 or type 2 diabetes |
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Have immunosuppressive disease |
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Are currently receiving immunosuppressive treatment or |
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Are 55 years of age AND have |
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cardiovascular disease (CVD), OR |
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hypertension, OR |
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chronic obstructive pulmonary disease (COPD) or other chronic respiratory disease |
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Are 12-17 years of age (inclusive) AND satisfy at least one of the following at the time of screening |
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Have a body mass index (BMI) 85th percentile for their age and gender based on CDC growth charts, <https://www.cdc.gov/growthcharts/clinical_charts.htm> |
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Have sickle cell disease |
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Have congenital or acquired heart disease |
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Have neurodevelopmental disorders, for example, cerebral palsy |
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Have a medical-related technological dependence, for example, tracheostomy, gastrostomy, or positive pressure ventilation (not related to COVID-19) |
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Have asthma or reactive airway or other chronic respiratory disease |
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Have type 1 or type 2 diabetes |
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Have immunosuppressive disease, or |
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Have chronic kidney disease |
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Are currently receiving immunosuppressive treatment |
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Have oxygen saturation (SpO2) less than or equal to ()93 percent (%) on room air at sea level or ratio of arterial oxygen partial pressure (PaO2 in millimeters of mercury) to fractional inspired oxygen (FiO2) less than (<)300, respiratory rate greater than or equal to ()30 per minute, heart rate 125 per minute |
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Require mechanical ventilation or anticipated impending need for mechanical ventilation |
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Have known allergies to any of the components used in the formulation of the interventions |
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Have hemodynamic instability requiring use of pressors within 24 hours of randomization |
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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 |
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Have any co-morbidity requiring surgery within <7 days, or that is considered life-threatening within 29 days |
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Have any serious concomitant systemic disease, condition or disorder that, in the opinion of the investigator, should preclude participation in this study |
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Have a history of a positive SARS-CoV-2 test prior to the one serving as eligibility for this study |
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Have received an investigational intervention for SARS-CoV-2 prophylaxis within 30 days before dosing |
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Have received treatment with a SARS-CoV-2 specific monoclonal antibody |
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Have a history of convalescent COVID-19 plasma treatment |
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Have participated in a previous SARS-CoV-2 vaccine study |
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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 |
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Are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study |
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Are pregnant or breast feeding |
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Have body weight <40 kilograms (kg) |
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