Evaluating the Efficacy of Convalescent Plasma in Symptomatic Outpatients Infected With COVID-19

Metro Infectious Disease Consultants

Status and phase: Completed; Phase 2

Conditions: COVID-19

Treatments: Biological: CCP

Study type: Interventional

Funder types: Other

Identifiers

NCT04438057

MIDC-CCP

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 103 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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103 participants in 2 patient groups

Standard of Care

No Intervention group

Description:

Patient will receive standard of care therapy.

Treatment Arm

Active Comparator group

Description:

Patient will receive convalescent plasma

Treatment:

Biological: CCP