Official Title
A Phase 1, Multi-Center, Open-Label, Safety and Tolerability Study of Intravenous Administration of ST266 in Subjects With Confirmed COVID-19 Infection
Brief Summary

The primary aim of the study is to evaluate the safety and tolerability of open-label ST266 given to subjects with confirmed COVID-19 infection through IV administration once a day of 5 consecutive days.

Detailed Description

This clinical trial will utilize a 3+3 enrollment design with sentinel approach.

Completed
Cytokine Release Syndrome

Biological: ST266

1X ST266

Eligibility Criteria

Inclusion Criteria:

1. Males and non-pregnant/non-breastfeeding females age 18-70 years of age.

2. Laboratory confirmed SARS-CoV-2 infection determined by PCR or other commercial/public
health assay (test results must be obtained within 7-days of the Screening Visit).

3. BMI between 18 and 39 inclusive, with a maximum weight of 150 kg (330lbs).

4. Asymptomatic or mildly symptomatic COVID-19 positive subject with a score of 1 or 2 on
the WHO 7-point ordinal scale.

5. Subjects with pulse oximetry of > 94% on room air

6. Subjects have controlled blood pressure of < 160/100 mmHg or systolic BP > 90 mmHg (or
20 mmHg less than usual range, whichever is higher)

7. Subjects with pulse < 120 bpm

8. Willingness and ability to comply with study-related procedures and assessments.

9. If female, subjects must use an effective method of birth control or abstain from
sexual relations with a male partner (unless has undergone tubal ligation or is 1 year
postmenopausal) for their duration of study participation.

10. If male, subjects must use an effective method of birth control or abstain from sexual
relations with a female partner (unless has undergone a vasectomy and it has been more
than 6 months) for their duration of study participation.

11. Subject or subject's legal representative provides written consent prior to the
initiation of any Screening or study specific procedures.

Exclusion Criteria:

1. Subjects requiring immediate admission to the hospital due to complications of
COVID-19 infection.

2. Subject has an untreated active bacterial, fungal, viral or other infection not
related to COVID-19 infection.

3. Subjects with chronic lung diseases of any etiology including idiopathic pulmonary
fibrosis, Tuberculosis, COPD, persistent asthma, and pulmonary hypertension.

4. Subjects with a severe history of cardiac disease (such as congestive heart failure,
coronary artery disease, cardiac arrhythmia)

5. Subjects with a history of neurological disorders (such as epilepsy, stroke,
encephalopathy, Guillain-Barré syndrome)

6. Subjects with D-dimer > 2 ug/mL

7. Subjects with a history of coagulopathy or currently taking anti-coagulation
medication

8. Subjects with PTT ≥ 100s or INR ≥ 2.75

9. Malignancy in the last 5 years (except successfully treated basal cell carcinoma).

10. Stage 4 severe chronic kidney disease or requiring dialysis (i.e., eGFR < 30).

11. Subjects with a reactive or positive screening test result For Hepatitis A virus
immunoglobulin M (HAV IgM), Hepatitis B Surface Antigen (HBsAg), Hepatitis C Virus
Antibody (HCVAb) or Human Immunodeficiency Virus Antibody (HIVAb).

12. TBIL> 2×ULN, ALT > 3×ULN, AST> 3×ULN, or ALP> 3×ULN.

13. Neutrophils <1000/mm3, PLT<50×10^9/L, or HGB<8g/dL

14. Previous participation in any other interventional clinical trial for the treatment
for COVID-19.

15. Subject actively participating in any other clinical study (with the exception of
observational studies where there is no intervention with an investigational product
or device)

16. Use of anti-cancer or immunomodulatory biological drug or kinase inhibitor (e.g.,
tocilizumab, sarilumab) or, JAK inhibitors (within 30 days of enrollment or five times
the half-life [whichever is longer]).

17. Chronic glucocorticosteroid use equivalent to daily oral prednisone > 10 mg per day
(10 mg oral prednisone every other day is allowed).

18. Live (live-attenuated) vaccines are not permitted within 2 weeks prior to enrollment
or during the study treatment and safety follow-up periods, including the SARS-CoV-2
vaccine (with the exception of the Flu vaccine which is allowed at any time)

19. Subject is pregnant or breastfeeding or plans to become pregnant within 12 months.

20. Subjects with a history of alcohol or drug abuse, or the use of illicit drugs within
the 12 months prior to Screening or use of medical marijuana within 1 month prior to
Screening.

21. Subject is considered by the Investigator, for any reason, to be an unsuitable
candidate for the study.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 70 Years
Countries
United States
Locations

Innovative Research of West Florida
Clearwater, Florida, United States

Great Lakes Clinical Trials
Chicago, Illinois, United States

WR-ClinSearch, LLC
Chattanooga, Tennessee, United States

David L Steed, MD, Study Director
Noveome Biotherapeutics, Inc

IQVIA Biotech
NCT Number
Keywords
Covid-19
MeSH Terms
COVID-19
Cytokine Release Syndrome