Collection of Anti-SARS-CoV-2 Immune Plasma
NCT04344977 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 151
Last updated 2021-03-05
Summary
Background:
The human disease caused by SARS-CoV-2 is called COVID-19. In most cases, COVID-19 is a mild to moderate respiratory illness. But it can also be more severe and even lead to death. There is no vaccine to prevent SARS-CoV-2 infection. There is also no therapy to treat COVID-19. Researchers want to collect plasma from adults who have recovered from COVID-19, which may help them develop treatments.
Objective:
To collect anti-SARS-CoV-2 immune plasma from adult volunteers who have recovered from COVID-19.
Eligibility:
Males and females ages 18 to 70 who have a history of COVID-19 like illness or positive test for SARS-CoV-2, and have a minimum level of SARS-CoV-2 antibodies as specified by the study.
Design:
This study consists of 2 parts: 1) screening for SARS-CoV-2 antibody titer and eligibility to donate plasma and 2) plasma collection by apheresis. Study sites may participate in 1 part alone (either screening or plasma collection only) or both parts (screening and plasma collection).
For screening part: Participants will be screened for their eligibility to join this research study with a medical history and physical exam. Their vital signs (blood pressure, heart rate, temperature, respiration rate) will be taken. Their weight and height will be recorded. They will give a blood sample for clinical laboratory tests of their general health and a research test for SARS-CoV-2 antibodies. They will discuss their history of COVID-19-like illness and any testing for SARS-CoV-2. They will be evaluated for their ability to donate plasma.
For plasma collection part: Subjects meeting criteria for plasma donation and found to have high neutralizing antibody titers and who plan to donate plasma under this part of the study will be scheduled for 1 (and up to 20) plasma collection sessions. These will occur no less than 7 days apart.
Prior to each donation, participants will have a brief physical exam and complete a donor history questionnaire. They will be asked about any current SARS-CoV-2 infection symptoms.
At each donation, plasma will be taken through a standard apheresis procedure. For this, blood will be withdrawn through a needle placed in the participant's arm vein. A machine will separate the plasma from the red cells. The red cells will be returned to the participant, either through the same needle or through a second needle in the other arm.
Participation may last up to 240 days.
Conditions
- Coronavirus Disease 2019 (COVID-19)
Sponsors & Collaborators
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-06-01
- Primary Completion
- 2020-11-20
- Completion
- 2021-03-03
Countries
- United States
Study Locations
More Related Trials
-
COVID-19 Convalescent Plasma
NCT04340050 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
COVID-19 Convalescent Plasma Treatment in SARS-CoV-2 Infected Patients
NCT04474340 ·Status: UNKNOWN ·Phase: PHASE1
-
Convalescent Plasma as Treatment for Acute Coronavirus Disease (COVID-19)
NCT04390178 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Convalescent Plasma for the Treatment of COVID-19 (Coronavirus Disease 2019)
NCT04554992 ·Status: COMPLETED ·Phase: PHASE1
-
SARS-COV2 Pandemic Serosurvey and Blood Sampling
NCT04334954 ·Status: COMPLETED
-
Efficacy of Convalescent Plasma Therapy in Patients With COVID-19
NCT04425915 ·Status: COMPLETED ·Phase: PHASE3
-
Convalescent Plasma vs. Standard Plasma for COVID-19
NCT04344535 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
COVID-19 Plasma Collection
NCT04344015 ·Status: COMPLETED ·Phase: NA
-
Treatment Of CORONAVIRUS DISEASE 2019 (COVID-19) With Anti-Sars-CoV-2 Convalescent Plasma (ASCoV2CP)
NCT04360486 ·Status: NO_LONGER_AVAILABLE
-
Convalescent Plasma Therapy - Zurich Protocol
NCT04869072 ·Status: COMPLETED ·Phase: PHASE1
-
A Longitudinal Study of COVID-19 Sequelae and Immunity
NCT04411147 ·Status: ACTIVE_NOT_RECRUITING
-
Efficacy and Safety of Convalescent Plasma in Treating COVID-19 Hospitalized Patients
NCT04354831 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy of Reinforcing Standard Therapy in COVID-19 Patients With Repeated Transfusion of Convalescent Plasma
NCT04803370 ·Status: COMPLETED ·Phase: NA
-
An Observational Cohort Trial of Outcomes and Antibody Responses Following Treatment With COVID19 Convalescent Plasma in Hospitalized COVID-19 Patients
NCT04471051 ·Status: COMPLETED
-
COVID-19 Convalescent Plasma for Mechanically Ventilated Population
NCT04388527 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Efficacy of Convalescent Plasma in Symptomatic Outpatients Infected With COVID-19
NCT04438057 ·Status: COMPLETED ·Phase: PHASE2
-
Convalescent Plasma to Limit SARS-CoV-2 Associated Complications
NCT04373460 ·Status: COMPLETED ·Phase: PHASE2
-
Use of Convalescent Plasma for COVID-19
NCT04408040 ·Status: TERMINATED ·Phase: PHASE2
-
Efficacy of Convalescent Plasma to Treat COVID-19 Patients, a Nested Trial in the CORIMUNO-19 Cohort
NCT04345991 ·Status: COMPLETED ·Phase: PHASE2
-
Anti-SARS-CoV-2 Inactivated Convalescent Plasma in the Treatment of COVID-19
NCT04292340 ·Status: UNKNOWN
-
Convalescent Plasma in Outpatients With COVID-19
NCT04355767 ·Status: COMPLETED ·Phase: PHASE3
-
Convalescent Plasma for Early Treatment of COVID-19
NCT04390503 ·Status: TERMINATED ·Phase: PHASE2
-
Plasma Therapy of COVID-19 in Severely Ill Patients
NCT04359810 ·Status: COMPLETED ·Phase: PHASE2
-
Convalescent Plasma for Treatment of COVID-19 Patients With Pneumonia
NCT04374565 ·Status: COMPLETED ·Phase: PHASE2
-
Convalescent Plasma as Treatment for Hospitalized Subjects With COVID-19 Infection
NCT04343755 ·Status: TERMINATED ·Phase: PHASE2