inclusion criteria: * confirmed positive for covid-19 by rt-pcr assay or equivalent * subject or family member/caregiver must have provided written informed consent which includes signing the institutional review board (irb) or independent ethics committee (iec) approved consent form prior to participating in any study related activity. however, if obtaining written informed consent is not possible, other procedures as provided in the march 27, 2020 (updated on july 2, 2020) fda guidance on conduct of clinical trials of medical products during covid-19 pandemic, question 10, may be used * able to swallow capsules * willing to follow contraception guidelines

inclusion criteria: * confirmed positive for covid-19 by rt-pcr assay or equivalent * subject or family member/caregiver must have provided written informed consent which includes signing the institutional review board (irb) or independent ethics committee (iec) approved consent form prior to participating in any study related activity. however, if obtaining written informed consent is not possible, other procedures as provided in the march 27, 2020 (updated on july 2, 2020) fda guidance on conduct of clinical trials of medical products during covid-19 pandemic, question 10, may be used * able to swallow capsules * willing to follow contraception guidelines

inclusion criteria: - confirmed positive for covid-19 by rt-pcr assay or equivalent - subject or family member/caregiver must have provided written informed consent which includes signing the institutional review board (irb) or independent ethics committee (iec) approved consent form prior to participating in any study related activity. however, if obtaining written informed consent is not possible, other procedures as provided in the march 27, 2020 (updated on july 2, 2020) fda guidance on conduct of clinical trials of medical products during covid-19 pandemic, question 10, may be used - able to swallow capsules - willing to follow contraception guidelines

inclusion criteria: - confirmed positive for covid-19 by rt-pcr assay or equivalent - subject or family member/caregiver must have provided written informed consent which includes signing the institutional review board (irb) or independent ethics committee (iec) approved consent form prior to participating in any study related activity. however, if obtaining written informed consent is not possible, other procedures as provided in the march 27, 2020 (updated on july 2, 2020) fda guidance on conduct of clinical trials of medical products during covid-19 pandemic, question 10, may be used - able to swallow capsules - willing to follow contraception guidelines