Convalescent Plasma for COVID-19 Patients (CPCP)

Vinmec Research Institute of Stem Cell and Gene Technology

Status and phase

Completed

Early Phase 1

Conditions

COVID 19

Treatments

Biological: Convalescent COVID 19 Plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT04516954

ISC.20.11.1

Details and patient eligibility

About

The investigators propose to evaluate intravenous administration of convalescent plasma (CP) obtained from COVID19 survivors in COVID19 patients who are in the medium stage. Supportive data exist for use of convalescent plasma in the treatment of COVID19 and other overwhelming viral illnesses. The study team wants to test the hypothesis that treatment with COVID19 CP will demonstrate salutary effects on COVID19 disease severity/duration, with the primary objective to reduce mortality. In addition, a major secondary objective to reduce the requirement for and/or duration of mechanical ventilation. The first phase is to test the safety of CP therapy.

Full description

Coronaviruses are among the most common causes of the common cold in humans.1,2 In recent decades, coronavirus has caused several epidemic worldwide with a vast number of deaths such as severe acute respiratory syndrome-SARS (2003) with 8098 people infected and 774 people died over 29 countries. The disease caused by SARS CoV-2 (COVID19) is manifest by fever, fatigue, dry cough, pharyngitis, and headache. In addition to the common clinical presentation of respiratory distress, and increasing frequency of cardiovascular manifestations has become evident.

In this context, the investigators propose to evaluate the safety of intravenous administration of convalescent plasma (CP) obtained from COVID19 survivors in patients requiring hospitalization for symptomatic "high risk" COVID19 disease. The study team wants to test the hypothesis that treatment with COVID19 CP will demonstrate salutary effects on COVID19 disease severity/duration, with the primary objective to reduce mortality. In addition, a major secondary objective to reduce the requirement for and/or duration of mechanical ventilation This is a single-arm, non-randomized, open-label treatment of eligible subjects defined as those who satisfy all inclusion criteria.

Written informed consent will be obtained all eligible subjects prior to participation.

Convalescent plasma will be obtained from male donors, nulliparous females, or female donors negative for HLA antibodies at least 14 days following recovery from COVID-19 infection.

Enrollment

4 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18-75 years
SARS-CoV-19 PCR positive
Medium stage
Time from onset to screening ≤ 21 days, the SARS-CoV-2 test is still positive

Exclusion criteria

Patients with a history of autoimmune disease or IgA deficiency
Patients with a history of allergy
Multi-organ/system failure
Pregnant or breastfeeding at the time of study
Cancer, history of heart failure, stroke, bronchial asthma
Multi-organ/system failure with indications for dialysis, severe hypoxia, failure with conventional treatment methods, indications for ECMO.
The patient is infected with multidrug-resistant bacteria.
The patient is participating in another study.
Time from onset to screening> 21 days