Convalescent Plasma Therapy vs. SOC for the Treatment of COVID-19 in Hospitalized Patients

Cristina Avendaño Solá350 enrolled

Overview

A total of 278 patients are planned. All patients will be in an early-stage of COVID-19. They must be adults and hospitalized. In this study, all participating patients will receive the standard treatment provided according to the current treatment protocols for coronavirus disease. In addition to this treatment, each patient will be randomly assigned to receive additional treatment with convalescent plasma transfusion (CP; blood plasma from patients who have been cured of coronavirus), or continue with standard treatment but without adding transfusion. 50% of the chances of additional treatment with CP, and 50% of the chances of receiving only the standard treatment for coronavirus. The duration of the study shall be one month from the assignment of the treatment. The patient and the doctor will know the treatment assigned.

A multi-center, randomized, clinical trial with two arms to study the efficacy and safety of passive immunotherapy with CP compared to a control of standard of care (SOC). All trial participants will receive SOC: * Treatment arm: Pathogen-reduced CP from patients recovered from COVID-19, whom, for the purpose of this trial, are herein designated as donors. * Control arm: SOC for COVID-19. Randomization among the two arms will be 1:1 and will be stratified per center. Of note, in the current status of a worldwide pandemic for which we have no approved vaccines or drugs, for the purpose of this trial SOC would also accept any drugs that are being used in clinical practice (e.g. lopinavir/ritonavir; darunavir/cobicistat; hydroxy/chloroquine, tocilizumab, etc.), other than those used as part of another clinical trial. The study is planned with a sequential design. Interim analyses: comprehensive safety data monitoring analyses will be conducted when 20%, 40%, 60% and 80% of patients, or at the discretionary DSMB criteria when needed. A DSMB charter will be set before the trial initiation where criteria for prematurely stopping the trial due to safety issues will be set. Interim analyses will be predefined upfront based on the DSMB recommendations.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Written informed consent prior to performing study procedures. Witnessed oral consent will be accepted in order to avoid paper handling. Written consent by patient or representatives will be obtained as soon as possible. 2. Male or female adult patient ≥18 years of age at time of enrolment. 3. Has laboratory-confirmed SARS-CoV-2 infection as determined by PCR in naso/oropharyngeal swabs or any other relevant specimen in the ongoing COVID-19 symptomatic period. Alternative test (i.e antigenic tests) are also acceptable as laboratory confirmation if their adequate specificity has been accepted by the sponsor. 4. Patients requiring hospitalization for COVID-19 without mechanical ventilation (invasive or non-invasive) or high flow oxygen devices and at least one of the following: * Radiographic evidence of pulmonary infiltrates by imaging (chest x-ray, CT scan, etc.), OR * Clinical assessment (evidence of rales/crackles on exam) AND SpO2 ≤ 94% on room air that requires supplemental oxygen. 5. No more than 7 days between the onset of symptoms (fever or cough) and treatment administration day. Exclusion Criteria: 1. Requiring mechanical ventilation (invasive or non-invasive) or high flow oxygen devices. 2. More than 7 days since symptoms (fever or cough). 3. Participation in any other clinical trial of an experimental treatment for COVID-19. 4. In the opinion of the clinical team, progression to death is imminent and inevitable within the next 24 hours, irrespective of the provision of treatments. 5. Any incompatibility or allergy to the administration of human plasma. 6. Stage 4 severe chronic kidney disease or requiring dialysis (i.e. eGFR \<30).

Locations (29)

Hospital Clínico Universitario Lozano Blesa

Zaragoza, Aragon, Spain

Hospital Universitario Mútua Terrassa

Terrassa, Barcelona, Spain

Hospital Universitario Puerta de Hierro Majadahonda

Majadahonda, Madrid, Spain

Hospital General de Albacete

Albacete, Spain

Hospital del Mar

Barcelona, Spain

Outcomes

Primary Outcomes

Category Changes in the "7-Ordinal Scale"

Proportion of patients in categories 5, 6 or 7 of the 7-point ordinal scale at day 15 7- Ordinal scale: 1. Not hospitalized, no limitations on activities. 2. Not hospitalized, limitation on activities. 3. Hospitalized, not requiring supplemental oxygen. 4. Hospitalized, requiring supplemental oxygen. 5. Hospitalized, on non-invasive ventilation or high flow oxygen devices. 6. Hospitalized, on invasive mechanical ventilation or ECMO. 7. Death.

Time frame: 15 days

Secondary Outcomes

Status at day 30 in the "7-point ordinal scale"

Time frame: 30 days

Time to category 5, 6 or 7 of the " 7-Ordinal scale"

Time to change from baseline category to worsening into 5,6 or 7 categories of the "7-Ordinal scale"

Time frame: 29 days

Time to an improvement of one category from admission in the "7-Ordinal scale"

Time frame: 29 days

Time to first deterioration

Time frame: 60 days

Mean change in the ranking in the "7-Ordinal scale" from baseline to days 3,5,8,11,15,29 and 60

Mean change in the ranking in the "7-Ordinal Scale" from baseline to days 3,5,8,11,15,29 and 60

Time frame: 60 days

Mean change in the ranking in the "11-Ordinal scale from baseline to days 3,5,8,11,15,29 and 60.

Mean change in the ranking in the "11- Ordinal scale" from baseline to days 3,5,8,11,15,29 and 60.

Time frame: 60 days

Status at day 15 and 30 in the "11-Ordinal scale"

Status at day 15 and 30 in the "11-Ordinal scale" Status at day 15 and 30 in the "11-Ordinal scale"

Time frame: 30 days

Mortality of any cause at 15 days

Rate of mortality of any cause within first 15 days.

Time frame: 15 days

Mortality of any cause at 28 days (day 29)

Rate of mortality of any cause within first 28 days.

Time frame: 28 days (day 29)

Mortality of any cause at 60 days

Rate of mortality of any cause within first 60 days.

Time frame: 60 days

Oxygenation free days

days free from oxygen supplementation

Time frame: 29 days

Ventilator free days

days free from mechanical ventilation

Time frame: 29 days

Duration of hospitalization (days)

days of hospitalization

Time frame: 60 days

Incidence of thrombotic arterial events

incidence of thrombotic arterial events

Time frame: 60 days

Incidence of thrombotic venous events

incidence of thrombotic venous events

Time frame: 60 days

Status at day 30 in the "11-Ordinal scale"

Status at day 30 in the "11-Ordinal scale" "11-Ordinal scale" : 0\. Uninfected ; no viral RNA detected. 1. Asymptomatic; viral RNA detected, limitation on activities. 2. Symptomatic; independent 3. Symptomatic; assistance needed 4. Hospitalized, no oxygen therapy. 5. Hospitalized, oxygen by mask or nasal prongs 6. Oxygen by mask or nasal prongs 7. Intubation and mechanical ventilation, pO2/FiO2 ≥150 or SpO2/FiO2 ≥200 8. Mechanical ventilation pO2/FIO2 \<150 (SpO2/FiO2 \<200) or vasopressors 9. Mechanical ventilation pO2/FiO2 \<150 and vasopressors, dialysis, or ECMO 10. Dead

Time frame: 30 days

Infusion-related adverse events

Infusion-related adverse events Cumulative incidence of serious adverse events (SAEs) Cumulative incidence of Grade 3 and 4 adverse events (AEs).

Time frame: 60 days

Incidence of Treatment-Emergent Adverse Events

cumulative incidence of Grade 3 and 4 adverse events (AEs) Cumulative incidence of serious adverse events (SAEs) Cumulative incidence of Grade 3 and 4 adverse events (AEs).

Time frame: 60 days

rate of rehospitalizations

rehospitalizations

Time frame: 60 days

Antibodies levels in CP donors recovered from COVID-19

Quantitative total antibodies and neutralizing antibody activity against SARSCoV-2 in the sera from donors and patients using viral pseudotypes

Time frame: 3 months

Viral load

Change in PCR for SARS-CoV-2 in naso/oropharyngeal swabs at baseline and at discharge

Time frame: Days 1,3,5,8,11,15, 29 and 60

Viral load

Change in PCR for SARS-CoV-2 in blood on Days 3,5,8,11,15,29 and 60 (while hospitalized) until two of them are negative consecutively

Time frame: Days 1,3,5,8,11,15,29 and 60

Convalescent Plasma Therapy vs. SOC for the Treatment of COVID-19 in Hospitalized Patients

Overview

Conditions

Interventions

Eligibility

Locations (29)

Outcomes

Primary Outcomes

Secondary Outcomes