This study will provide investigational convalescent plasma for patients infected with the SARS-CoV-2 with mild to moderate symptoms who meet inclusion criteria as judged by physician evaluation.
This study will provide investigational convalescent plasma for patients infected with the
SARS-CoV-2 with mild to moderate symptoms who meet inclusion criteria as judged by physician
evaluation.
Following patient enrollment into the study, completion of informed consent and
randomization, the patient will receive one unit of convalescent COVID plasma or standard of
care. The plasma will be infused in an outpatient infusion center by highly trained and
experienced staff. Vitalant will be providing the plasma as per their normal screening and
distribution protocols. Patients will be monitored for safety during the infusion and per
protocol following the infusion for a period of 28 days. Primary efficacy and safety
endpoints will be statistically analyzed and compared between the two groups.
Biological: CCP
Randomized open label study to receive 2:1 CCP to standard of care
Other Name: convalescent plasma
Inclusion Criteria:
- Laboratory confirmed diagnosis of infection with SARS-CoV-2
- Symptoms of COVID -19 - cough, fever, sore throat, SOB, anosmia, diarrhea, myalgia
- Symptoms less than 14 days
- ID Physician determination that the patient does not need hospitalization
- O2 saturation of >93%
- Informed consent provided by the patient or healthcare proxy
- Age ≥ 18 years
- Ambulatory Outpatient when informed consent obtained and study drug is administered
Exclusion Criteria:
- Age < 18 y/o
- Patients currently receiving intravenous immunoglobulin
- Hypercoagulable state - neoplasia, Collagen vascular disease, Myelodysplastic
syndrome, chronic anticoagulation treatment, etc.
- Need to be hospitalized
- O2 sat < 93%
- D-Dimer > 2x normal
- Chronic oxygen therapy
- Renal insufficiency with Creatinine clearance < 30
- Long term care or assisted living facility resident
- Ongoing usage of hydroxychloroquine for any indication
- History of blood or plasma transfusion related complications
- Enrollment into any other investigational drug or device study within the previous 30
days
- Any drug, chemical or alcohol dependency as determined by the investigator through
history that may affect study procedures and follow up
- Pregnant or breast feeding
- Any acute or chronic medical comorbidity, psychiatric, social or other circumstance
that, in the opinion of the investigator, may interfere with study compliance,
completion, or accurate assessment of the study outcomes/safety
- Admitted to or expected to be admitted to a medical facility
Metro Infectious Disease Consultants
Burr Ridge, Illinois, United States