COVID-19Phase 3CONCOR-1NCT04348656
CONvalescent Plasma for Hospitalized Adults With COVID-19 Respiratory Illness (CONCOR-1)
A Phase 3 study testing Convalescent plasma in people with COVID-19, run by Hamilton Health Sciences Corporation at 73 sites in 3 countries.
Trial summary
There is currently no treatment available for COVID-19, the acute respiratory illness caused by the novel SAR-CoV-2. Convalescent plasma from patients who have recovered from COVID-19 that contains antibodies to the virus is a potential therapy. Read more about this study
- Who is it for?
- Ages 16 years and older
- Conditions the study is for
- COVID-19
- What is being tested?
- Convalescent plasma
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 940 participants
- Where
- 73 sitesin 3 countries
- Study dates
- 14 Mar 2020to 16 Jun 2021
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- ≥16 years old (>18 years of age in the United States)
- Admitted to hospital with confirmed COVID-19 respiratory illness
- Receiving supplemental oxygen
- 500 mL of ABO compatible convalescent plasma is available
Who cannot join
- Onset of respiratory symptoms >12 days prior to randomization
- Intubated or plan in place for intubation
- Plasma is contraindicated (e.g. history of anaphylaxis from transfusion)
- Decision in place for no active treatment
Trial locations and contacts
73 sites in 3 countries.
73 sites in 3 countries
Canada68 sites
Fraser Health Authority - Abbotsford Regional Hospital and Cancer Centre
Abbotsford British Columbia, British Columbia, V2S 0C2
Lakeridge Health Ajax Pickering
Ajax, Ontario, L1S 2J4
Vitalité Health Network - Acadie-Bathurst
Bathurst, New Brunswick, E2A 4L7
Peter Lougheed Center
Calgary, Alberta, T1Y 6J4
Foothills Medical Centre
Calgary, Alberta, T2N 2T9
Rockyview General Hospital
Calgary, Alberta, T2V 1P9
Vitalité Health Network - Restigouche
Campbellton, New Brunswick, E3N 3G2
L'Hopital Chicoutimi
Chicoutimi, Quebec, G7H 5H6
University of Alberta - Royal Alexandra Hospital
Edmonton, Alberta, T5H 3V9
University of Alberta Hospital
Edmonton, Alberta, T6G 2B7
Vitalité Health Network- Northwest
Edmundston, New Brunswick, E3V 4E4
Hamilton General Hospital
Hamilton, Ontario, L8L 2X2
Juravinski Hospital
Hamilton, Ontario, L8V 1C3
St. Joseph's Healthcare
Hamilton, Ontario, M6R 1B5
Grand River Hospital
Kitchener, Ontario, N2G 1G3
St. Mary's Hospital
Kitchener, Ontario, N2M 1B2
Hôpital de la Cité-de-la-Santé
Laval, Quebec, H7M 3L9
Hotel Dieu Hospital of Lévis
Lévis, Quebec, G6V 3Z1
London Health Sciences Centre - University Hospital
London, Ontario, N6A 5A5
Victoria Hospital
London, Ontario, N6A 5W9
Hôpital Charles-Le Moyne
Longueuil, Quebec, J4V 2H1
Markham Stouffville Hospital
Markham, Ontario, L3P 7P3
Trillium Health Partners - Mississauga Hospital
Mississauga, Ontario, L5B 1B8
Trillium Health Partners - Credit Valley
Mississauga, Ontario, L5M 2N1
Dr. Georges-L.-Dumont University Hospital Centre
Moncton, New Brunswick, E1C 2Z3
Hôpital Maisonneuve-Rosemont
Montreal, Quebec, H1T 2M4
Centre hospitalier de l'Université de Montréal
Montreal, Quebec, H2X 3E4
Montréal General Hospital
Montreal, Quebec, H3G 1A4
Centre hospitalier universitaire Sainte-Justine
Montreal, Quebec, H3T 1C5
Jewish General Hospital
Montreal, Quebec, H3T 1E2
McGill University Health Centre
Montreal, Quebec, H4A 3J1
Hôpital du Sacré-Coeur de Montreal
Montreal, Quebec, H4J 1C5
North York General Hospital
North York, Ontario, M2K 1E1
Lakeridge Health Oshawa
Oshawa, Ontario, L1G 2B9
Ottawa Hospital - General Campus
Ottawa, Ontario, K1H 8L6
Ottawa Hospital - Civic Campus
Ottawa, Ontario, K1Y 4E9
Queensway Carleton Hospital
Ottawa, Ontario, K2H 8P4
Centre Hospitalier Universitaire (CHU) de Québec - Université Laval
Québec, Quebec, G1R 2J6
Institut Universitaire de cardiologie et pneumologie de Québec
Québec, Quebec, G1V 4G5
Regina General Hospital
Regina, Saskatchewan, S4P 0W5
Pasqua Hospital
Regina, Saskatchewan, S4T 1A5
Niagara Health System - St. Catherines
Saint Catherines, Ontario, L2S 0A9
Centre hospitalier régional de St-Jérôme
Saint-Jérôme, Quebec, J7Z 5T3
Bluewater Health
Sarnia, Ontario, N7T 6S3
St. Paul's Hospital
Saskatoon, Saskatchewan, S7M 0Z9
Royal University Hospital
Saskatoon, Saskatchewan, S7N 0W8
Scarborough Health Network, Centenary Hospital
Scarborough Village, Ontario, M1E 4B9
Scarborough Health Network, General Hospital
Scarborough Village, Ontario, M1P 2V5
Scarborough Health Network, Birchmount Hospital
Scarborough Village, Ontario, M1W 3W3
Centre Hospitalier Universitaire de Sherbrooke (CHUS) - Hôpital Hôtel-Dieu
Sherbrooke, Quebec, J1G 2E8
Centre Hospitalier Universitaire de Sherbrooke (CHUS) - Hôpital Fleurimont
Sherbrooke, Quebec, J1H 5H3
Sturgeon Community Hospital
St. Albert, Alberta, T8N 6C4
Sunnybrook Health Sciences Centre
Toronto, Ontario, M4N 3M5
Unity Health St. Michael's Hospital
Toronto, Ontario, M5B 1W8
Sinai Health System
Toronto, Ontario, M5G 1X5
Toronto General Hospital
Toronto, Ontario, M5G 2C4
Toronto Western Hospital
Toronto, Ontario, M5T 2S8
Unity Health, St. Joseph's Health Care Centre
Toronto, Ontario, M6R 1B5
Centre hospitalier affilié universitaire régional de Trois-Rivières
Trois-Rivières, Quebec, G8Z 3R9
Vancouver General Hospital
Vancouver, British Columbia, V5Z 1M9
St. Paul's Hospital
Vancouver, British Columbia, V6Z 1Y6
Royal Jubilee Hospital
Victoria, British Columbia, V8R 1J8
Victoria General Hospital
Victoria, British Columbia, V8Z 6R5
Windsor Regional Hospital - Metropolitan Campus
Windsor, Ontario, N8W 1L9
Windsor Regional Hospital - Ouellette Campus
Windsor, Ontario, N9A 1E1
St. Boniface General Hospital
Winnipeg, Manitoba, R2H 2A6
Health Sciences Centre Winnipeg
Winnipeg, Manitoba, R3A 1R9
Grace General Hospital
Winnipeg, Manitoba, R3J 3M7
United States3 sites
Brooklyn Hospital
Brooklyn, New York, 11201
Lower Manhattan Hospital
New York, New York, 10038
Weill Cornell Medical Center
New York, New York, 10065
Brazil2 sites
Hospital Universitário Antônio Pedro (HUAP)
Niterói, 24070-035
Hemario
Rio de Janeiro, 20211-030
About this study
Official title: A Randomized Open-Label Trial of CONvalenscent Plasma for Hospitalized Adults With Acute COVID-19 Respiratory Illness (CONCOR-1)
There is currently no treatment available for COVID-19, the acute respiratory illness caused by the novel SAR-CoV-2. Convalescent plasma from patients who have recovered from COVID-19 that contains antibodies to the virus is a potential therapy. On March 25th, 2020, the FDA approved the use of convalescent plasma under the emergency investigational new drug (eIND) category. Randomized trials are needed to determine the efficacy and safety of COVID-19 convalescent plasma for acute COVID-19 infection.
The objective of the CONCOR-1 trial is to determine the efficacy of transfusion of COVID-19 convalescent plasma to adult patients admitted to hospital with COVID-19 infection at decreasing the frequency of in-hospital mortality in patients hospitalized for COVID-19.
Read more
It is hypothesized that treating hospitalized COVID-19 patients with convalescent plasma early in their clinical course will reduce the risk of death, and that other outcomes will be improved including risk of intubation, and length of ICU and hospital stay.
This pan-Canadian clinical trial has the potential to improve patient outcomes and reduce the burden on health care resources including reducing the need for ICU beds and ventilators.
Read the detailed description
Problem to be addressed: In December 2019, the Wuhan Municipal Health Committee (Wuhan, China) identified an outbreak of viral pneumonia cases of unknown cause. Coronavirus RNA was quickly identified in some of these patients.This novel coronavirus has been designated SARS-CoV-2, and the disease caused by this virus has been designated COVID-19.Outbreak forecasting and mathematical modelling suggest that these numbers will continue to rise [1] in many countries over the coming weeks to months.Global efforts to evaluate novel antivirals and therapeutic strategies to treat COVID-19 have intensified. There is an urgent public health need for rapid development of novel interventions. At present, there is no specific antiviral therapy for coronavirus infections.
Passive immunization:Passive immunization consists in the transfer of antibodies from immunized donor to non-immunized individual in order to transfer transient protection against an infective agent. A physiological example of passive immunization is the transfer of maternal IgG antibodies to the foetus through the placenta to confer humoral protection to newborns in the first years of life. Passive immunization differs from active immunization in which the patient develops their own immune response following contact with the infective agent or vaccine.
Known potential risks and benefits: There is a theoretical risk of antibody-dependent enhancement of infection (ADE) through which virus targeted by non-neutralizing antibodies gain entry into macrophages. Another theoretical risk is that antibody administration to those exposed to SARS-CoV-2 may avoid disease but modify the immune response such that those individuals mount attenuated immune responses, which would leave them vulnerable to subsequent re-infection. Finally, there are risks associated with any transfusion of plasma including transmission of blood transmitted viruses (e.g. HIV, HBV, HCV, etc.), allergic transfusion reactions, including anaphylaxis, febrile non hemolytic transfusion reaction, transfusion related acute lung injury (TRALI), transfusion associated cardiac overload (TACO), and hemolysis should ABO incompatible plasma be administered. Potential benefits of COVID-19 convalescent plasma include improved survival, improvement in symptoms, decreased risk in intubation for mechanical ventilation, decrease risk of intensive care unit (ICU) admission, shortened hospitalization time and suppression of viral load.
Mechanism of action: Transfusion of apheresis frozen plasma (AFP) from COVID-19 convalescent patients allows the transfer of donor neutralizing antibodies directed against SARS-CoV2 antigens to the recipient, thus allowing the generation of passive immunization. Naturally produced human antibody are polyclonal, meaning they are directed against a variety of different viral antigens and epitopes allowing for a general neutralizing effect against the virus rather than focussing on a specific target. Administration of convalescent plasma has been associated with rapid decrease in viral load. It is also possible that passive immunization contributes to improved cell-mediated immunity by favoring the phagocytosis and presentation of viral antigens to host T cells.
Participant recruitment:Only hospitalized COVID-19 patients are eligible so recruitment efforts will be focused on identified consecutive patients admitted to hospital with acute COVID-19 infection. No other external recruitment efforts are planned. At each participating hospital, a process for identifying patients with COVID-19 will be established.
Donor recruitment for Canadian sites: Recovered COVID-19 patients will be identified as potential donors in collaboration with provincial public health services, local health authorities, and individual co-investigators involved in the study. Potential donors may also be recruiting following self-identification on the routine donor questionnaire or through social media. They will be contacted by phone and invited to participate in the program as potential donors. After obtaining verbal consent and reviewing donor selection criteria, eligible participants will be directed to a Héma-Québec collection or Canadian Blood Services apheresis collection site in their area to donate.
Criteria for donors: All donors will need to meet the criteria set forth in the Manual of donor selection criteria in use at Héma-Québec or Canadian Blood ServicesIn addition, donors will require:
- Prior diagnosis of COVID-19 documented by a PCR test at time of infection or by positive anti-SARS-CoV-2 serology following infection
- Male donors, or female donors with no pregnancy history or with negative anti-HLA antibodies
- At least 6 days since last plasma donation
- Provided informed consent
- A complete resolution of symptoms at least 14 days prior to donation
Donor recruitment for United States sites: Recovered COVID-19 patients are being recruited through the New York Blood Center and Weill Cornell Medicine in separate protocols. Potential donors can self-refer via websites but also be referred by physicians or identified via the medical record system. Only donors with laboratory-confirmed history of COVID-19 will be screened. After providing consent and reviewing FDA and NYBC donor eligibility criteria, donors are screened for the presences of SARS-CoV-2 virus in the nasopharynx if screening within 14 days of complete resolution in accordance with current FDA guidance. Criteria for donation are subject to change based on future revision of FDA guidance. Those found to be eligible will be referred to NYBC for donation.
Criteria for donors:
- Provision of informed consent
- Aged 18 to 70 years. Donors are not longer eligible after their 71st birthday.
- Documented molecular diagnosis of SARS-CoV-2 by RT-PCR by nasopharyngeal swab, oropharyngeal swab, or sputum or detection of anti-SARS-CoV-2 IgG in serum.
- Complete resolution of COVID-19 symptoms at least 14 days prior to donation
- Not currently pregnant or pregnant within 6 weeks by self-report
- Male donors, or females with no pregnancy history or with negative anti-HLA antibodies
- Meets blood donor criteria specified by NYBC, which is consistent with FDA regulations.
Donors will be allowed to donate every 7 days. The following information will be collection from donors: ABO group, sex, age, date of onset of symptoms (when available), date of resolution of symptoms (when available), CCP collection date(s).
Randomization procedures: Patients will be randomized in a 2:1 ratio (convalescent plasma vs standard of care). Patients will be randomized using a secure, concealed, computer-generated, web-accessed randomization sequence. Randomization will be stratified by centre and age (<60 and ≥ 60 years). Within each stratum, variable permuted block sized will be used. This approach will ensure that concealment of the treatment sequence is maintained.
Duration of follow-up: Subjects will be followed daily until hospital discharge or death. Patients discharged from hospital before Day 30 will be contacted by telephone on Day 30 ± 3 days to ascertain any AEs, vital status (dead/alive), hospital readmission and need for mechanical ventilation after discharge. Patients discharged from hospital will be contacted at Day 90+/- 7 days to determine vital status. Patients with a prolonged hospital admission will be censored at Day 90. The local study coordinator will collect all study data and record the data in the electronic CRF or paper CRF as per study procedures for each site.
Duration of study: For an individual subject, the study ends 90 days after randomization. The overall study will end when the last randomized subject has completed 90 day follow-up. We estimate that all patient will be enrolled in a period of 6 months, data on the primary endpoint will be available 30 days after last patient enrollment and data on all secondary endpoints will be available after 90-day from last patient enrollment.
Sample size considerations: Assuming a baseline risk of intubation or death of 30% in hospitalized patients with standard of care, a sample size of 1200 (800 in the convalescent plasma arm, and 400 in the standard of care arm) would provide 80% power to detect a relative risk reduction of 25% with convalescent plasma therapy using a 2-tailed test at level α = 0.05 and a 2:1 randomization.
Interim analysis: A single interim analysis is planned when the primary outcome (intubation or mortality at 30 days) is available for 50% of the target sample. An O'Brien-Fleming stopping rule will be used at that time, but treated as a guideline, so there is minimal impact on the threshold for statistical significance for the final significance test of the primary outcome. A DSMB will monitor ongoing results to ensure patient well-being and safety as well as study integrity. The DSMB will be asked to recommend early termination or modification only when there is clear and substantial evidence of a treatment difference.
Final analysis plan: The primary analysis will be based on the intention-to-treat population which will include data from all individuals who have been randomized. Outcomes will be attributed to the arm to which individuals were randomized irrespective of whether they received the planned intervention (e.g. plasma from a convalescent COVID-19 donor).
- Conditions
- COVID-19
- Being tested
- Convalescent plasma
- Keywords
- Convalescent plasma, Transfusion, SARS-CoV-2, Passive immunization
- Medical subject headings
- COVID-19
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Convalescent plasmaBiological
Patients will receive 500 mL of convalescent plasma (from one single-donor unit of 500 mL or 2 units of 250 mL from 1-2 donations) collected by apheresis from donors who have recovered from COVID-19 and frozen (1 year expiration date from date of collection). The plasma unit will be thawed as per standard blood bank procedures and infused into the patient slowly over 4 hours. When administering 2 units of 250 mL, the 2nd unit will be administered after the first, and no longer than 12 hours later. The patient will be monitored for adverse events as per each site's policies.
| Study group | Role | What they receive |
|---|---|---|
| Convalescent plasma | Experimental | ~500 mL ABO compatible convalescent apheresis plasma Receives: Biological: Convalescent plasma |
| Standard of care | No intervention | Treated as per institutional standard of care. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants Who Were Intubated or Died
Endpoint of the need for intubation or patient death
Measured: Day 30
Secondary outcomes (16)
Time to Intubation or In-hospital Death
Time in days from randomization to occurrence of intubation or death
Measured: Day 30
Ventilator-free Days by Day 30
Number of days off ventilator at 30 days
Measured: Day 30
Death by Day 30
Occurrence of patient death at 30 days
Measured: Day 30
Length of Stay in Intensive Care Unit (ICU)
Number of days spent in the intensive care unit (ICU) over the 30-day period following randomization
Measured: Day 30
Need for Renal Replacement Therapy
Need for new renal replacement therapy
Measured: Day 30
Need for Extracorporeal Membrane Oxygenation (ECMO)
Requirement for extracorporeal membrane oxygenation (ECMO)
Measured: Day 30
Development of Myocarditis
New diagnosis of myocarditis
Measured: Day 30
In-hospital Death
Occurrence of death while in hospital, censored at 90 days. Patients who were still in hospital at Day 30 were followed until Day 90 to capture in-hospital mortality.
Measured: Day 90
Time to In-hospital Death
Time to in-hospital death at 90 days. Patients who were still in hospital at Day 30 were followed until Day 90 to capture in-hospital mortality.
Measured: Day 90
Length of Stay in Hospital
Number of days from randomization to death or hospital discharge. Patients still in hospital at Day 30 were followed until Day 90 to capture death or discharge from hospital.
Measured: Day 90
Number of Participants With Grade 3 and 4 Serious Adverse Events
Number of participants with Grade 3 and 4 (CTCAE v4.0) serious adverse events, and cumulative incidence of Grade 3 and 4 serious adverse events (using MedDRA AE terms)
Measured: Day 30
Number of Participants With CCP Transfusion-associated Adverse Events (AE)
Number of participants experiencing CCP transfusion-associated adverse events (AE), as defined by the International Society of Blood Tranfusion (ISBT ) classification
Measured: Day 30
Number of Participants With Grade 3, 4, or 5 Serious Adverse Events
Number of Participants with Grade 3-5 (CTCAE v4.0) serious adverse events reported to Day 30
Measured: Day 30
Patient Reported Outcome Using Change in EQ-5D-5L Score
Change in score on EQ-5D-5L instrument at Day 30 as compared to baseline. The EQ-5D-5L measures health-related quality of life in five dimensions, namely, mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Patients can report five level impairment, reflecting no, slight, moderate, severe, and extreme problems in each dimension. The range of possible values is -0.148 to 0.949, with a higher score reflecting a better outcome. For the change in score, a positive number indicates that the scores improved from baseline.
Measured: Baseline and Day 30
Patient Reported Outcome- Quality-adjusted Life Days
Quality-adjusted life days calculated using the EQ-5D-5L score. Quality-adjusted life days is a measure of how well a patient lives for how long. It combines the length of life and quality of life into one value. This is calculated by multiplying the health utility (derived from the EQ-5D-5L score) by the amount of time the patient is alive during the study period. A higher number is better.
Measured: Day 30
Cost of Intervention and Hospital Stay
Cost per patient calculated using cost of the intervention and costs of the hospital stay
Measured: Day 30
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Apr 2020
- Study start14 Mar 2020
- Primary completion5 Mar 2021
- Study completion16 Jun 2021
Why it stopped: Study was terminated after the planned interim analysis as the pre-defined futility threshold was met
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for COVID-19Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 940 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hamilton Health Sciences Corporation
- Sponsor type
- University, hospital or other
- Collaborators
- Canadian Blood Services, Héma-Québec, University of Toronto, Université de Montréal, Weill Medical College of Cornell University, New York Blood Center
- Responsible party
- Sponsor
- Investigators
- Donald M Arnold, MD, Principal investigator, McMaster University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04348656
- Sponsor's protocol ID
- CONCOR-1
- Acronym
- CONCOR-1
- Status last verified
- Mar 2022
- First submitted
- 13 Apr 2020
- Last updated
- 3 Mar 2022
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Wu JT, Leung K, Leung GM. Nowcasting and forecasting the potential domestic and international spread of the 2019-nCoV outbreak originating in Wuhan, China: a modelling study. Lancet. 2020 Feb 29;395(10225):689-697. doi: 10.1016/S0140-6736(20)30260-9. Epub 2020 Jan 31.
PubMed 320141142. FDA USFDA. Investigational COVID-19 Convalescent Plasma - Emergency INDs [Web]. 2020 [Available from: https://www.fda.gov/vaccines-blood-biologics/investigational-new-drug-ind-or-device-exemption-ide-process-cber/investigational-covid-19-convalescent-plasma-emergency-inds accessed March 26th 2020.
Begin P, Callum J, Jamula E, Cook R, Heddle NM, Tinmouth A, Zeller MP, Beaudoin-Bussieres G, Amorim L, Bazin R, Loftsgard KC, Carl R, Chasse M, Cushing MM, Daneman N, Devine DV, Dumaresq J, Fergusson DA, Gabe C, Glesby MJ, Li N, Liu Y, McGeer A, Robitaille N, Sachais BS, Scales DC, Schwartz L, Shehata N, Turgeon AF, Wood H, Zarychanski R, Finzi A; CONCOR-1 Study Group; Arnold DM. Convalescent plasma for hospitalized patients with COVID-19: an open-label, randomized controlled trial. Nat Med. 2021 Nov;27(11):2012-2024. doi: 10.1038/s41591-021-01488-2. Epub 2021 Sep 9.
PubMed 34504336Begin P, Callum J, Heddle NM, Cook R, Zeller MP, Tinmouth A, Fergusson DA, Cushing MM, Glesby MJ, Chasse M, Devine DV, Robitalle N, Bazin R, Shehata N, Finzi A, McGeer A, Scales DC, Schwartz L, Turgeon AF, Zarychanski R, Daneman N, Carl R, Amorim L, Gabe C, Ellis M, Sachais BS, Loftsgard KC, Jamula E, Carruthers J, Duncan J, Lucier K, Li N, Liu Y, Armali C, Kron A, Modi D, Auclair MC, Cerro S, Avram M, Arnold DM. Convalescent plasma for adults with acute COVID-19 respiratory illness (CONCOR-1): study protocol for an international, multicentre, randomized, open-label trial. Trials. 2021 May 4;22(1):323. doi: 10.1186/s13063-021-05235-3.
PubMed 33947446
Study at a glance
From the registry record, last updated by the sponsor on 3 Mar 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized Open-Label Trial of CONvalenscent Plasma for Hospitalized Adults With Acute COVID-19 Respiratory Illness (CONCOR-1)
- ClinicalTrials.gov ID
- NCT04348656
- Acronym / sponsor ID
- CONCOR-1 / CONCOR-1
- Conditions
- COVID-19
- Keywords
- Convalescent plasma, Transfusion, SARS-CoV-2, Passive immunization
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Study was terminated after the planned interim analysis as the pre-defined futility threshold was met
- Enrolment
- 940 participants (actual)
- Lead sponsor
- Hamilton Health Sciences CorporationUniversity, hospital or other
- Collaborators
- Canadian Blood Services, Héma-Québec, University of Toronto, Université de Montréal, Weill Medical College of Cornell University, New York Blood Center
- Study start
- 14 Mar 2020 (actual)
- Primary completion
- 5 Mar 2021 (actual)
- Study completion
- 16 Jun 2021 (actual)
- First posted
- 16 Apr 2020 (actual)
- Results
- Posted 3 Mar 2022
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
There is currently no treatment available for COVID-19, the acute respiratory illness caused by the novel SAR-CoV-2. Convalescent plasma from patients who have recovered from COVID-19 that contains antibodies to the virus is a potential therapy. On March 25th, 2020, the FDA approved the use of convalescent plasma under the emergency investigational new drug (eIND) category. Randomized trials are needed to determine the efficacy and safety of COVID-19 convalescent plasma for acute COVID-19 infection.
The objective of the CONCOR-1 trial is to determine the efficacy of transfusion of COVID-19 convalescent plasma to adult patients admitted to hospital with COVID-19 infection at decreasing the frequency of in-hospital mortality in patients hospitalized for COVID-19.
It is hypothesized that treating hospitalized COVID-19 patients with convalescent plasma early in their clinical course will reduce the risk of death, and that other outcomes will be improved including risk of intubation, and length of ICU and hospital stay.
This pan-Canadian clinical trial has the potential to improve patient outcomes and reduce the burden on health care resources including reducing the need for ICU beds and ventilators.
Detailed description
Problem to be addressed: In December 2019, the Wuhan Municipal Health Committee (Wuhan, China) identified an outbreak of viral pneumonia cases of unknown cause. Coronavirus RNA was quickly identified in some of these patients.This novel coronavirus has been designated SARS-CoV-2, and the disease caused by this virus has been designated COVID-19.Outbreak forecasting and mathematical modelling suggest that these numbers will continue to rise [1] in many countries over the coming weeks to months.Global efforts to evaluate novel antivirals and therapeutic strategies to treat COVID-19 have intensified. There is an urgent public health need for rapid development of novel interventions. At present, there is no specific antiviral therapy for coronavirus infections.
Passive immunization:Passive immunization consists in the transfer of antibodies from immunized donor to non-immunized individual in order to transfer transient protection against an infective agent. A physiological example of passive immunization is the transfer of maternal IgG antibodies to the foetus through the placenta to confer humoral protection to newborns in the first years of life. Passive immunization differs from active immunization in which the patient develops their own immune response following contact with the infective agent or vaccine.
Known potential risks and benefits: There is a theoretical risk of antibody-dependent enhancement of infection (ADE) through which virus targeted by non-neutralizing antibodies gain entry into macrophages. Another theoretical risk is that antibody administration to those exposed to SARS-CoV-2 may avoid disease but modify the immune response such that those individuals mount attenuated immune responses, which would leave them vulnerable to subsequent re-infection. Finally, there are risks associated with any transfusion of plasma including transmission of blood transmitted viruses (e.g. HIV, HBV, HCV, etc.), allergic transfusion reactions, including anaphylaxis, febrile non hemolytic transfusion reaction, transfusion related acute lung injury (TRALI), transfusion associated cardiac overload (TACO), and hemolysis should ABO incompatible plasma be administered. Potential benefits of COVID-19 convalescent plasma include improved survival, improvement in symptoms, decreased risk in intubation for mechanical ventilation, decrease risk of intensive care unit (ICU) admission, shortened hospitalization time and suppression of viral load.
Mechanism of action: Transfusion of apheresis frozen plasma (AFP) from COVID-19 convalescent patients allows the transfer of donor neutralizing antibodies directed against SARS-CoV2 antigens to the recipient, thus allowing the generation of passive immunization. Naturally produced human antibody are polyclonal, meaning they are directed against a variety of different viral antigens and epitopes allowing for a general neutralizing effect against the virus rather than focussing on a specific target. Administration of convalescent plasma has been associated with rapid decrease in viral load. It is also possible that passive immunization contributes to improved cell-mediated immunity by favoring the phagocytosis and presentation of viral antigens to host T cells.
Participant recruitment:Only hospitalized COVID-19 patients are eligible so recruitment efforts will be focused on identified consecutive patients admitted to hospital with acute COVID-19 infection. No other external recruitment efforts are planned. At each participating hospital, a process for identifying patients with COVID-19 will be established.
Donor recruitment for Canadian sites: Recovered COVID-19 patients will be identified as potential donors in collaboration with provincial public health services, local health authorities, and individual co-investigators involved in the study. Potential donors may also be recruiting following self-identification on the routine donor questionnaire or through social media. They will be contacted by phone and invited to participate in the program as potential donors. After obtaining verbal consent and reviewing donor selection criteria, eligible participants will be directed to a Héma-Québec collection or Canadian Blood Services apheresis collection site in their area to donate.
Criteria for donors: All donors will need to meet the criteria set forth in the Manual of donor selection criteria in use at Héma-Québec or Canadian Blood ServicesIn addition, donors will require:
- Prior diagnosis of COVID-19 documented by a PCR test at time of infection or by positive anti-SARS-CoV-2 serology following infection
- Male donors, or female donors with no pregnancy history or with negative anti-HLA antibodies
- At least 6 days since last plasma donation
- Provided informed consent
- A complete resolution of symptoms at least 14 days prior to donation
Donor recruitment for United States sites: Recovered COVID-19 patients are being recruited through the New York Blood Center and Weill Cornell Medicine in separate protocols. Potential donors can self-refer via websites but also be referred by physicians or identified via the medical record system. Only donors with laboratory-confirmed history of COVID-19 will be screened. After providing consent and reviewing FDA and NYBC donor eligibility criteria, donors are screened for the presences of SARS-CoV-2 virus in the nasopharynx if screening within 14 days of complete resolution in accordance with current FDA guidance. Criteria for donation are subject to change based on future revision of FDA guidance. Those found to be eligible will be referred to NYBC for donation.
Criteria for donors:
- Provision of informed consent
- Aged 18 to 70 years. Donors are not longer eligible after their 71st birthday.
- Documented molecular diagnosis of SARS-CoV-2 by RT-PCR by nasopharyngeal swab, oropharyngeal swab, or sputum or detection of anti-SARS-CoV-2 IgG in serum.
- Complete resolution of COVID-19 symptoms at least 14 days prior to donation
- Not currently pregnant or pregnant within 6 weeks by self-report
- Male donors, or females with no pregnancy history or with negative anti-HLA antibodies
- Meets blood donor criteria specified by NYBC, which is consistent with FDA regulations.
Donors will be allowed to donate every 7 days. The following information will be collection from donors: ABO group, sex, age, date of onset of symptoms (when available), date of resolution of symptoms (when available), CCP collection date(s).
Randomization procedures: Patients will be randomized in a 2:1 ratio (convalescent plasma vs standard of care). Patients will be randomized using a secure, concealed, computer-generated, web-accessed randomization sequence. Randomization will be stratified by centre and age (<60 and ≥ 60 years). Within each stratum, variable permuted block sized will be used. This approach will ensure that concealment of the treatment sequence is maintained.
Duration of follow-up: Subjects will be followed daily until hospital discharge or death. Patients discharged from hospital before Day 30 will be contacted by telephone on Day 30 ± 3 days to ascertain any AEs, vital status (dead/alive), hospital readmission and need for mechanical ventilation after discharge. Patients discharged from hospital will be contacted at Day 90+/- 7 days to determine vital status. Patients with a prolonged hospital admission will be censored at Day 90. The local study coordinator will collect all study data and record the data in the electronic CRF or paper CRF as per study procedures for each site.
Duration of study: For an individual subject, the study ends 90 days after randomization. The overall study will end when the last randomized subject has completed 90 day follow-up. We estimate that all patient will be enrolled in a period of 6 months, data on the primary endpoint will be available 30 days after last patient enrollment and data on all secondary endpoints will be available after 90-day from last patient enrollment.
Sample size considerations: Assuming a baseline risk of intubation or death of 30% in hospitalized patients with standard of care, a sample size of 1200 (800 in the convalescent plasma arm, and 400 in the standard of care arm) would provide 80% power to detect a relative risk reduction of 25% with convalescent plasma therapy using a 2-tailed test at level α = 0.05 and a 2:1 randomization.
Interim analysis: A single interim analysis is planned when the primary outcome (intubation or mortality at 30 days) is available for 50% of the target sample. An O'Brien-Fleming stopping rule will be used at that time, but treated as a guideline, so there is minimal impact on the threshold for statistical significance for the final significance test of the primary outcome. A DSMB will monitor ongoing results to ensure patient well-being and safety as well as study integrity. The DSMB will be asked to recommend early termination or modification only when there is clear and substantial evidence of a treatment difference.
Final analysis plan: The primary analysis will be based on the intention-to-treat population which will include data from all individuals who have been randomized. Outcomes will be attributed to the arm to which individuals were randomized irrespective of whether they received the planned intervention (e.g. plasma from a convalescent COVID-19 donor).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Convalescent plasma | Experimental | Biological: Convalescent plasma~500 mL ABO compatible convalescent apheresis plasma |
| Standard of care | No intervention | –Treated as per institutional standard of care. |
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (4 listed)
- ≥16 years old (>18 years of age in the United States)
- Admitted to hospital with confirmed COVID-19 respiratory illness
- Receiving supplemental oxygen
- 500 mL of ABO compatible convalescent plasma is available
Key exclusion criteria (4 listed)
- Onset of respiratory symptoms >12 days prior to randomization
- Intubated or plan in place for intubation
- Plasma is contraindicated (e.g. history of anaphylaxis from transfusion)
- Decision in place for no active treatment
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Convalescent plasmaPatients will receive 500 mL of convalescent plasma (from one single-donor unit of 500 mL or 2 units of 250 mL from 1-2 donations) collected by apheresis from donors who have recovered from COVID-19 and frozen (1 year expiration date from date of collection). The plasma unit will be thawed as per standard blood bank procedures and infused into the patient slowly over 4 hours. When administering 2 units of 250 mL, the 2nd unit will be administered after the first, and no longer than 12 hours later. The patient will be monitored for adverse events as per each site's policies. | Biological | Convalescent plasma |
Primary outcome
Number of Participants Who Were Intubated or Died
Time frame: Day 30
Endpoint of the need for intubation or patient death
16 secondary outcomes
Time to Intubation or In-hospital Death
Time frame: Day 30
Ventilator-free Days by Day 30
Time frame: Day 30
Death by Day 30
Time frame: Day 30
Length of Stay in Intensive Care Unit (ICU)
Time frame: Day 30
Need for Renal Replacement Therapy
Time frame: Day 30
Need for Extracorporeal Membrane Oxygenation (ECMO)
Time frame: Day 30
Development of Myocarditis
Time frame: Day 30
In-hospital Death
Time frame: Day 90
Time to In-hospital Death
Time frame: Day 90
Length of Stay in Hospital
Time frame: Day 90
Number of Participants With Grade 3 and 4 Serious Adverse Events
Time frame: Day 30
Number of Participants With CCP Transfusion-associated Adverse Events (AE)
Time frame: Day 30
Number of Participants With Grade 3, 4, or 5 Serious Adverse Events
Time frame: Day 30
Patient Reported Outcome Using Change in EQ-5D-5L Score
Time frame: Baseline and Day 30
Patient Reported Outcome- Quality-adjusted Life Days
Time frame: Day 30
Cost of Intervention and Hospital Stay
Time frame: Day 30
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Mar 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Background: PubMed 32014114Wu JT, Leung K, Leung GM. Nowcasting and forecasting the potential domestic and international spread of the 2019-nCoV outbreak originating in Wuhan, China: a modelling study. Lancet. 2020 Feb 29;395(10225):689-697. doi: 10.1016/S0140-6736(20)30260-9. Epub 2020 Jan 31.
- Background2. FDA USFDA. Investigational COVID-19 Convalescent Plasma - Emergency INDs [Web]. 2020 [Available from: https://www.fda.gov/vaccines-blood-biologics/investigational-new-drug-ind-or-device-exemption-ide-process-cber/investigational-covid-19-convalescent-plasma-emergency-inds accessed March 26th 2020.
- Derived from this study: PubMed 34504336Begin P, Callum J, Jamula E, Cook R, Heddle NM, Tinmouth A, Zeller MP, Beaudoin-Bussieres G, Amorim L, Bazin R, Loftsgard KC, Carl R, Chasse M, Cushing MM, Daneman N, Devine DV, Dumaresq J, Fergusson DA, Gabe C, Glesby MJ, Li N, Liu Y, McGeer A, Robitaille N, Sachais BS, Scales DC, Schwartz L, Shehata N, Turgeon AF, Wood H, Zarychanski R, Finzi A; CONCOR-1 Study Group; Arnold DM. Convalescent plasma for hospitalized patients with COVID-19: an open-label, randomized controlled trial. Nat Med. 2021 Nov;27(11):2012-2024. doi: 10.1038/s41591-021-01488-2. Epub 2021 Sep 9.
- Derived from this study: PubMed 33947446Begin P, Callum J, Heddle NM, Cook R, Zeller MP, Tinmouth A, Fergusson DA, Cushing MM, Glesby MJ, Chasse M, Devine DV, Robitalle N, Bazin R, Shehata N, Finzi A, McGeer A, Scales DC, Schwartz L, Turgeon AF, Zarychanski R, Daneman N, Carl R, Amorim L, Gabe C, Ellis M, Sachais BS, Loftsgard KC, Jamula E, Carruthers J, Duncan J, Lucier K, Li N, Liu Y, Armali C, Kron A, Modi D, Auclair MC, Cerro S, Avram M, Arnold DM. Convalescent plasma for adults with acute COVID-19 respiratory illness (CONCOR-1): study protocol for an international, multicentre, randomized, open-label trial. Trials. 2021 May 4;22(1):323. doi: 10.1186/s13063-021-05235-3.
- Publication of trial results in Nature MedicineLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Donald M Arnold, MD principal investigator
McMaster University
73 sites in 3 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Convalescent plasma in people with COVID-19, run by Hamilton Health Sciences Corporation at 73 sites in 3 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 3 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 73 sites in Canada, United States, Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 3 Mar 2022). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of Participants Who Were Intubated or Died (time frame: Day 30). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04348656, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2022.