Inclusion Criteria:

Otherwise healthy, positive for COVID-19 by an EUA-approved rapid antigen or PCR test, has ongoing “mild to moderate illness or symptoms” with symptom onset starting < 5 days prior to screening visits Must provide written informed consent/assent if a minor which includes signing the institutional review board/independent ethics committee approved consent form prior to participating in any study related activity Willing and able to comply with study procedures and follow-up visits Willing to follow all contraception guidelines Exclusion

Exclusion Criteria:

In the Investigator's opinion, has progressive symptoms with likely imminent (24-48 hours) hospitalization or severe COVID-19 illness/symptoms Any medical condition that, in the Investigator's or designee's opinion, could adversely impact participant safety or key objectives of the study Has a prior history of long COVID Has a clinically documents acute infection other than COVID-19 Known or suspected pregnancy, planned pregnancy, a positive pregnancy test at screening or are breastfeeding Has participated, or is participating in a clinical reserach study evaluating COVID-19 convalescent plasma, mAbs against SARS-CoV-2, or IV immunoglobulin within 2 months or less than 5 half-lives of the investigational product (whichever is longer) prior to the screening visit