Official Title
Efficacy and Safety of High-Titer Anti-SARS-CoV-2 (COVID19) Convalescent Plasma for Hospitalized Patients With Infection Due to COVID-19 to Decrease Complications: A Phase II Trial
Brief Summary

This is a single arm phase II trial to assess efficacy and confirm safety of infusions of anti-SARS-CoV-2 convalescent plasma in hospitalized patients with acute respiratory symptoms,with or without confirmed interstitial COVID-19 pneumonia by chest Xray or CT. A total of 29 eligible subjects will be enrolled to receive anti-SARS-CoV-2 plasma.Outcomes will be compared to hospitalized controls with confirmed COVID-19 disease through retrospective chart review.

Detailed Description

There are no proven treatments for coronavirus disease (COVID-19) and associated pneumonia
caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Recent experience in
China suggests that convalescent immune plasma(CIP)may be an effective treatment for
COVID-19. In the pandemic situation where there are no vaccines for COVID-19, specific
antibodies in convalescent plasma induced by infection may provide passive protective
immunity. Passive antibody therapy was the first immunotherapy dating back to the 1890's for
the treatment of infectious diseases before the development of antibiotics 1940's. Experience
from prior outbreaks with other coronaviruses, such as SARS-CoV-1 shows that such
convalescent plasma contains neutralizing antibodies to the relevant virus. In SARS-CoV-2,
passive antibody therapy from CIP probably provided protection by viral neutralization. CIP
was also used in the 2013 Ebola epidemic. A small non-randomized study in Sierra Leone
revealed a significant increase in survival for who received CIP4. CIP administration is the
only approach that provides immediate immunity to patients who have been exposed or who have
active disease.

This approach is immediately available from individuals who have recovered, are viral
free,and can donate immune plasma (IP) containing high titer neutralizing antibodies. Passive
antibody therapy can be given to a patient recently exposed or a patient who is developing an
infection with COVID-19 by obtaining plasma units from immune individuals by standard
plasmapheresis using FDA-approved blood banking procedures, cross matching the unit(s) to the
recipients and infusing the unit(s) using standard transfusion procedures for blood products.
Based on the safety and long-term experience with plasma infusions, plasma exchanges, and
other procedures involving plasma or plasma product, this protocol was designed as a phase II
single arm trial that involves the administration of antibodies to a given agent to a
susceptible individual for the purpose of preventing or treating an infectious disease due to
that agent.

The only antibody formulation that is available for emergent use is that found in
convalescent plasma. As more individuals contract COVID-19 and recover, the number of
potential donors will increase.

The principle of passive antibody therapy is that it is more effective when used for
prophylaxis than for treatment of disease. When used for therapy, antibody is most effective
when administered shortly after the onset of symptoms. The reason for temporal variation in
efficacy is not well understood but could reflect that passive antibody works by neutralizing
the initial inoculum, which is likely to be much smaller than that of established disease.
Alternatively, antibodies may dampen the early inflammatory response leaving the infected
individual asymptomatic. For example, antibody therapy for pneumococcal pneumonia was most
effective when given shortly after the onset of symptoms and was of no benefit if antibody
therapy was delayed beyond the third day of disease. For passive antibody therapy to be
effective, a sufficient amount of antibody must be infused. The antibody will circulate in
the blood, reach tissues,and provide protection against infection. Depending on the type of
antibody, amount, and composition, the half-life can vary from weeks to months. It is under
these circumstances, the investigators plan to treat patients who are sick enough to be
hospitalized before the onset of overwhelming disease involving a systemic inflammatory
response, sepsis, and/or ARDS.

Completed
Corona Virus Infection
SARS-CoV 2
SARS Pneumonia
Pneumonia

Drug: High-Titer Anti-SARS-CoV-2 (COVID 19) Convalescent Plasma

Pathogen reduced SARS-CoV-2 convalescent plasma (1-2 units; ~200 mL each for a total of 200-400mls) given preferably in one day, but allowable to be given over 2 days if clinical circumstances delay infusions in 1 day), with titer to be determined after the unit has been infused.

Eligibility Criteria

Inclusion Criteria:

- Patients must be 18 years of age or older

- Patients hospitalized with COVID-19 respiratory symptoms within 72 hours of admission
to a"floor" bed (non-ICU bed) and confirmation via SARS-CoV-2 RT-PCR testing.

- Patient and/or surrogate is willing and able to provide written informed consent and
comply with all protocol requirements.

- Patients with hematologic malignancies or solid tumors are eligible.

- Patients with autoimmune disorders are eligible.

- Patients with immunodeficiency and organ or stem cell transplant recipients are
eligible.

- Patients who have received or are receiving hydroxychloroquine or chloroquine are
eligible (but will be taken off the drug)

- Prior use of IVIG is allowed but the investigator should consider the potential for a
hypercoagulable state.

Exclusion Criteria:

- Patients requiring mechanical ventilation or >6 liters per minute nasal cannula oxygen

- Patients on other anti-COVID-19 trials being treated with tocilizumab (anti-IL-6
receptor), Siltuximab (anti-IL-2), Remdesivir, or other pharmacological trials that
may be initiated hereafter.

- A pre-existing condition or use of a medication that, in the opinion of the site
investigator, may place the individual at a substantially increased risk of thrombosis
(e.g., cryoglobulinemia, severe refractory hypertriglyceridemia, or clinically
significant monoclonal gammopathy).

- Contraindication to transfusion or history of prior reactions to transfusion blood
products.

- Medical conditions for which receipt of 500-600 mL of intravenous fluid may be
dangerous to the subject (e.g., decompensated congestive heart failure).

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

University of Virginia Medical Center
Charlottesville, Virginia, United States

University of Virginia
Charlottesville, Virginia, United States

University of Virginia
NCT Number
MeSH Terms
Infections
Pneumonia
Coronavirus Infections