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Males and females at least 18 years of age or of legal consenting age based on local requirements.\n2. Persons at increased risk of contracting COVID-19, including:\n\n   1. Healthcare workers with known direct occupational exposure to COVID-19 within 7 days prior to enrollment. A qualifying person (i) provides healthcare to patients and\u002For (ii) typically positions themselves within 6 feet of patients (\"close contact\") and (iii) is a full- time employee (average of ≥ 24 hours\u002Fweek) in a high contact area (Emergency Department, Intensive Care Unit, COVID-specific Care Unit, Walk-in Clinic, Paramedic\u002FFirst Responder).\n   2. Persons participating in social activities without the practice of generally accepted social distancing practices at least three times per week. Qualifying activities include the presence of at least 10 people in close (\\\u003C6 feet) proximity to each other without masks or other personal protective equipment (e.g., socializing at bars or community\u002Fsocial centers, in-home social gatherings, classes or trainings, etc.). These subjects must have engaged in such activities at least three times in the past 7 days and plan to continue these activities during the study.\n3. Must have a smartphone, tablet, computer, or other qualifying internet- enabled device and daily internet access.\n4. Occupational exposure to a person infected with SAR-CoV-2 within 7 days prior to enrollment or social interaction as defined in criterion 2(b).\n5. Willing and able to provide written informed consent and comply with the requirements of the protocol, including completion of the subject diary.\n\nExclusion Criteria:\n\n1. Subjects not at increased risk of contracting SARS-CoV-2 from occupational or social behaviors.\n2. Subjects with known severe heart, lung, neurological or other systemic disease that the Investigator believes could preclude safe participation.\n3. Subjects with a history of COVID-19 or known to have developed anti- SARS-CoV-2 antibodies or received a SARS-CoV-2 vaccine.\n4. Subjects who experienced a previous episode of acute upper respiratory tract infection, otitis, bronchitis or sinusitis or received antibiotics for these conditions or antiviral therapy for influenza within two weeks prior to and including study day 1.\n5. Subjects residing in the same household with another family member currently participating in the study.\n6. Receipt of any dose of NTZ within 7 days prior to screening.\n7. Treatment with any investigational drug or vaccine therapy within 30 days prior to screening and willing to avoid them during the course of the study.\n8. Known sensitivity to NTZ or any of the excipients comprising the study medication.\n9. 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Female subjects are considered of childbearing potential unless they are postmenopausal (absence of menstrual bleeding for 1 year or 6 months if laboratory confirmation of hormonal status), or have had a hysterectomy, bilateral tubular ligation or bilateral oophorectomy.\n11. Females who are breastfeeding.\n12. Subjects with active respiratory allergies or subjects expected to require anti-allergy medications during the study period for respiratory allergies.\n13. Subjects taking medications considered to be major CYP2C8 substrates.\n14. Subjects who, in the judgment of the Investigator, will be unlikely to comply with the requirements of this protocol including completion of the subject diary.",false,"ALL","18 Years","120 Years",{"count":291,"type":292},1407,"ACTUAL","INTERVENTIONAL",[295],"PHASE3",[297,298],"COVID-19","Viral Respiratory Illnesses",[297,298],"COMPLETED","2024-06-18",{"date":303,"type":292},"2024-06-26",{"date":305,"type":292},"2020-05-13",{"date":307,"type":292},"2021-04-07",{"name":5,"class":6},26]