Inclusion Criteria:

1. Male or female, aged ≥18, regardless of COVID-19 vaccination status;

2. Laboratory confirmed infection COVID-19 disease as determined using an
FDA-authorized COVID-19 rapid antigen test;

3. Able and willing to give written informed consent;

4. Willing to complete the following study activities and assessments:

1. Keep an electronic diary from Study Days 2 through 42.

2. Have phone or videoconferences with study team personnel on Study Days 10, 21,
and 35.

3. Have study samples collected in-home on Days 5, 14, 28, and 42

4. Agree to return to clinic for additional safety evaluations if needed, as
determined by the study team;

5. An aggregate patient-reported COVID-19 symptom score of at ≥3 on the first day of
drug administration (Study Day 1).

6. Must agree not to enroll in another study of an investigational agent prior to
completion of Day 42 of the study;

7. Able to take ARAKODA according to Prescribing Information

8. Have been symptomatic no longer than 7 days inclusive of Day 1 when the first dose
of study medication is administered.

9. If female, agree to use an acceptable method of birth control from the time of
consent through 56 days after the last dose of study drug.

10. Possess a smart phone or tablet, or are willing to utilize a sponsor-provided device
if available.

Exclusion Criteria:

1. Have any of the contraindications for ARAKODA in the prescribing information
including:

1. G6PD deficiency

2. Breastfeeding

3. Psychotic disorder or current psychotic symptoms

4. Known hypersensitivity reaction to TQ

2. Evidence of severe or critical illness, defined by at least one of the following:

1. Clinical signs indicative of severe systemic illness with COVID-19, such as
respiratory rate ≥30 breaths per minute, heart rate ≥125 beats per minute, SpO2
≤93% on room air

2. Respiratory failure defined based on resource utilization requiring at least
one of the following: i. Endotracheal intubation and mechanical ventilation,
oxygen delivered by high flow nasal cannula (heated, humidified, oxygen
delivered via reinforced nasal cannula at flow rates >20 L/min with fraction of
delivered oxygen ≥0.5), noninvasive positive pressure ventilation,
extracorporeal membrane oxygenation (ECMO), or clinical diagnosis of
respiratory failure (i.e., clinical need for one of the preceding therapies,
but preceding therapies not able to be administered in setting of resource
limitation); ii. Shock (defined by systolic blood pressure <90 mmHg, or
diastolic blood pressure <60 mmHg or requiring vasopressors); iii. Multi-organ
dysfunction/failure

3. Any other clinically significant acute illness unrelated to COVID-19 within seven
days prior to first study drug administration;

4. Receipt of any approved or experimental small molecule treatment for COVID-19
(FDA-approved, off-label, compassionate use, or study-related) within the 30 days
prior to the time of the screening evaluation

5. Receipt of any approved or experimental biologic therapeutic for COVID-19
(FDA-approved, off-label, compassionate use, or study-related) within the 90 days
prior to the time of the screening evaluation

6. Have been diagnosed (and confirmed by PCR or rapid antigen test) with COVID-19 in
the 90 days prior to randomization (other than for this infection);

7. Any excluded concomitant medication as described in the ARAKODA package insert.
Receipt of a COVID-19 vaccine is not exclusionary;

8. Any COVID-19 symptoms which, in the opinion of the investigator, is suggestive of
possible requirement to hospitalize within 48 hours of enrollment.

9. Positive pregnancy test;

10. Are ≥65 years of age and have a clinical frailty score > 5;

11. Have cystic fibrosis;

12. Have received a transplant;

13. Known to be infected with human immunodeficiency virus (HIV);

14. Have received any B-Cell depleting monoclonal antibody in the last six months;

15. Have a disease or condition which in the opinion of the investigator presents an
unacceptable risk of disease progression;

16. Have an aggregate symptom score ≥ 15 and any one of the following risk factors for
COVID-19 disease progression: Obesity (BMI ≥31), are a smoker, have never been
vaccinated for COVID-19, diabetes with complications, dementia or other
neurocognitive disorders, chronic kidney disease, chronic liver disease, COPD or
other chronic lung disease, bronchiectasis, coronary atherosclerosis and other heart
disease, stroke or other cerebrovascular disease, sickle cell disease or
thalassemia, current mood disorder or depression, substance abuse disorder,
tuberculosis, cancer that is not invasive squamous and basal carcinomas of the skin
or prostate cancer under active surveillance;

17. Have two or more of the following risk factors for COVID-19 disease progression:
Obesity (BMI ≥31), are a smoker, diabetes with complications, dementia or other
neurocognitive disorders, chronic kidney disease, chronic liver disease, COPD or
other chronic lung disease, bronchiectasis, coronary atherosclerosis and other heart
disease, stroke or other cerebrovascular disease, sickle cell disease or
thalassemia, current mood disorder or depression, substance abuse disorder,
tuberculosis, cancer that is not invasive squamous and basal carcinomas of the skin
or prostate cancer under active surveillance;

18. Have an aggregate symptom score >32.