Evaluation of Activity and Safety of Two Regimens of Low Dose Oral Selinexor in Participants With Moderate or Severe COVID-19

Inclusion Criteria:

- Confirmed laboratory diagnosis of SARS-CoV2 by standard approved reverse transcription
polymerase chain reaction (RT-PCR) assay or equivalent approved testing (by local
labs).

- Currently hospitalized and consented within the first 48 hours of hospitalization.

- Informed consent provided as above (patients must be dosed with study drug within 12
hours of consent).

- Has symptoms of moderate or severe COVID-19 as demonstrated by:

Moderate COVID-19:

1. Currently hospitalized and requiring medical care for COVID-19, and

2. Peripheral capillary oxygen saturation (SpO2, pulse oximetry) > 94% on room air at
screening, and

3. Radiographic evidence of pulmonary infiltrates

Severe COVID-19:

1. At least one of the following: fever, cough, sore throat, malaise, headache, muscle
pain, shortness of breath at rest or with exertion, confusion, or symptoms of severe
lower respiratory symptoms including dyspnea at rest or respiratory distress AND

2. Clinical signs indicative of lower respiratory infection with COVID-19, with at least
one of the following: respiratory rate ≥ 30 breaths/minute (min), heart rate ≥
125/min, Oxygen saturation (SpO2) <93% on room air or requires > 2L/minute oxygen by
NC in order to maintain SaO2 ≥93%, PaO2/FiO2 <300 millimeter per mercury (mm/hg)

- Female patients of childbearing potential must have a negative serum pregnancy
test at Screening and must use highly effective methods of contraception
throughout the study and for 3 months following the last dose of study treatment.

- Males who are sexually active must commit to use a highly effective method of
contraception while receiving selinexor and for 3 months after the last selinexor
dose, or consent to total sexual abstinence (abstinence must occur from
enrollment and continue for 3 months after the last selinexor dose).

Exclusion Criteria:

- Evidence of critical COVID-19 based on:

1. Respiratory failure (defined by endotracheal intubation and mechanical
ventilation, oxygen delivered by high-flow nasal cannula, noninvasive positive
pressure ventilation, or clinical diagnosis of respiratory failure in setting of
resource limitations)

2. Septic shock (defined by SBP < 90 mm Hg, or Diastolic BP < 60 mm Hg)

3. Multiple organ dysfunction/failure

- In the opinion of the investigator, unlikely to survive for at least 48 hours from
screening or anticipate mechanical ventilation within 48 hours

- Concurrent anti-viral and/or anti-inflammatory agents (e.g., biologics,
hydroxychloroquine) are not permitted.

- Inadequate hematologic parameters as indicated by the following labs:

1. Patients with severe neutropenia (ANC <1,000 x 10^9/liter [L]) or

2. Thrombocytopenia (e.g., platelets <100,000 per microliter of blood)

- Inadequate renal function as indicated by creatinine clearance (CrCl) <20 milliliter
per minute (mL/min) using the formula of Cockcroft and Gault.

- Inadequate hepatic function defined as AST or ALT > 5x the upper limit of normal OR
serum direct bilirubin > 2.5x the upper limit of normal.

- Hyponatremia defined as sodium < 135 milliequivalents per liter (mEq/L).

- In the opinion of the Investigator, patients who are below their ideal body weight and
would be unduly impacted by changes in their weight.

- Unable to take oral medication when informed consent is obtained.

- Patients with a legal guardian or who are incarcerated.

- Pregnant and breastfeeding women.