| Eligibility |
Inclusion Criteria:
1. Female and male patients over the age of 18.
2. Confirmed COVID-19 infection by PCR analysis
3. Hospitalized at Soroka University Medical Center.
4. Display mild to moderate symptoms of respiratory infection (Temperature <39.0 oC,
respiratory rate < 25, O2 % Sat > 95% in room air or with supplemental oxygen through
nasal cannula, P/F ratio > 150).
5. Willing and able to convey informed consent.
6. Willing and able to comply with all study procedures
7. Female patients of childbearing potential and male patients with partners of
childbearing potential must agree to use adequate methods of contraception during the
study and through 90 days after the last dose of study medication. Female patients of
childbearing potential are all those except patients who are surgically sterile, who
have medically documented ovarian failure, or who are at least 1 year postmenopausal.
For females: 2 of the following contraceptive methods, with at least 1 being a barrier
method:
- Hormonal contraceptives for = 27 days before dosing
- Intrauterine device (IUD) in place = 27 days before dosing
- Double-barrier methods (use of condom [male partner] with either diaphragm with
spermicide or cervical cap with spermicide) from screening
- Surgical sterilization of the partner (vasectomy = 1 month before screening) Female
patients must have a negative urine pregnancy test (minimum sensitivity 25 IU/L or
equivalent units of human chorionic gonadotropin [hCG]) within 24 hours prior to the
start of investigational product.
For males:
- Surgical sterilization (vasectomy = 1 month before screening) Or
- Both of the following contraceptive methods from screening:
- Consistently and correctly use a condom
- Partner must use a hormonal contraceptive or a nonhormonal barrier method (IUD or
diaphragm with spermicide or cervical cap with spermicide).
Exclusion Criteria:
1. Treatment with interferons (IFNs) immunomodulators and/or immunosuppressive or B-cell
depleting medications within 12 months before screening.
2. Previous use of Interferon Lambda. Patients who previously participated in a clinical
trial of Interferon Lambda but are confirmed to have received placebo or another
non-Lambda IFNs are allowed.
3. History or evidence of any intolerance or hypersensitivity to IFNs.
4. Patients with respiratory infection requiring invasive or non-invasive ventilatory
support (bipap or intubation and mechanical ventilation).
5. Participation in a clinical trial with use of any investigational drug within 30 days
before screening.
6. History of any of the following diseases or conditions:
- Advanced or decompensated liver disease (presence or history of bleeding varices,
ascites, encephalopathy or hepato-renal syndrome)
- Immunologically mediated disease (e.g., rheumatoid arthritis, inflammatory bowel
disease, severe psoriasis, systemic lupus erythematosus) that requires more than
intermittent nonsteroidal anti-inflammatory medications for management or that
requires use of systemic corticosteroids in the 6 months before screening
(inhaled asthma medications are allowed).
- Retinal disorder or clinically relevant ophthalmic disorder.
- Any malignancy within 5 years before screening. Exceptions are superficial
dermatologic malignancies (e.g., squamous cell or basal cell skin cancer treated
with curative intent).
- Cardiomyopathy, significant ischemic cardiac or cerebrovascular disease
(including history of angina, myocardial infarction, or interventional procedure
for coronary artery disease), or cardiac rhythm disorder.
- Chronic pulmonary disease (e.g., chronic obstructive pulmonary disease)
associated with functional impairment.
- Pancreatitis.
- Severe or uncontrolled psychiatric disorder, e.g., depression, manic condition,
psychosis, acute and/or chronic cognitive dysfunction, suicidal behavior, and
relapse of substance abuse.
- Active seizure disorder defined by either an untreated seizure disorder or
continued seizure activity within the preceding year despite treatment with
anti-seizure medication.
- Bone marrow or solid organ transplantation
- Other significant medical condition that may require intervention during the
trial (such as uncontrolled diabetes or thyroid disease) Patients with any
serious condition that, in the opinion of the investigator, would preclude
evaluation of response or make it unlikely that the contemplated course of
therapy and follow-up could be completed. Patients for whom participation in the
trial would increase their risk.
- Current eating disorder
- Current alcohol abuse (excessive alcohol intake, defined as follows: >20 g/day
for females [1.5 standard alcohol drinks] or >30 g/day for males [2.0 standard
alcohol drinks]. A standard drink contains 14 g of alcohol: 360 mL of beer, 150
mL of wine, or 45 mL of spirits
- Drug abuse within the previous 6 months before screening, with the exception of
cannabinoids and their derivatives
7. Any of the following abnormal laboratory test in the 12 months prior to enrollment
- Platelet count <90,000 cells/mm3
- White blood cell (WBC) count <3,000 cells/mm3
- Absolute neutrophil count (ANC) <1,500 cells/mm3
- Hemoglobin <11 g/dL for women and <12 g/dL for men
- Estimated creatinine clearance (CrCl) < 50 mL/min by Cockroft-Gault formulation
- ALT and/or ALT levels > 10 times the upper limit of normal
- Bilirubin level = 2.5 mg/dL unless due to Gilbert's syndrome
- Serum albumin level <3.5 g/dL
- International normalized ratio (INR) =1.5 (except patients maintained on
anticoagulant medications)
|
