A randomized, open-label, 2 arm, pilot trial of Lambda 180 mcg administeredsubcutaneously once weekly, for up to two weeks (2 injections at most), in addition tostandard supportive care, compared to standard supportive care alone, in a population ofCOVID-19 infected patients.patients will be randomized according to 1:1 ratio to one of the 2 trial arms: Lambda 180mcg S.C + standard care (intervention arm) or standard care only (control arm).
Recently, a novel coronavirus (SARS-CoV-2) has been identified as the causative pathogen
of a rapidly spreading infection associated with pneumonia and severe acute respiratory
syndrome (COVID-19), for which there is currently no approved therapy. Interferon Lambda
(IFN Lambda) is a type III interferon with broad anti-viral activity and receptor
distribution limited to the respiratory and gastrointestinal epithelium. Studies in
animal models suggest that IFN Lambda may ameliorate infection with respiratory viruses
such as influenza coronaviruses. The WHO has recently included pegylated interferon
lambda in its landscape analysis of potential therapeutics for COVID-19.
In this randomized, open-label, 2 arms, pilot trial, up to 40 patients diagnosed with
COVID-19 and mild to moderate respiratory infection, will be randomized to one of 2
treatment arms in 1:1 ratio: 1. Lambda 180 mcg administered S.C once weekly, for up to
two weeks (2 injections at most) + standard care, Or 2. Standard care alone.
Efficacy of Lambda will be assessed by PCR analysis for COVID-19 (Fluxergy, Irvine CA),
from respiratory secretions obtained by nasopharyngeal and oropharyngeal swabs, collected
consecutively at day 1, 3, 5, 7, 10, 14 and 21 following initial diagnosis or until
patients are discharged following achievement of two consecutive PCR negative tests for
COVID-19. Safety and tolerability of Lambda will be assessed by adverse event (AE)
monitoring, vital signs assessment and clinical laboratory tests (CBC, and extended
chemistry panel).
Drug: Lambda 180 mcg S.C
Prefilled injection syringe of 180 microgram Pegylated interferon lambda, administered on
day 0 and if needed on day 7
Other Name: Lambda
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)
Soroka UMC
Be'er Sheva, Israel
Ohad Etzion, MD, Principal Investigator
Soroka Univeersity Medical Center