NCT04362176

Brief Summary

The purpose of this study is to test the safety and efficacy of convalescent donor plasma to treat COVID-19 in hospitalized adults in a randomized, placebo-controlled setting. The effect of convalescent plasma will be compared to placebo on clinical outcomes, measured using the COVID-19 7-point Ordinal Clinical Progression Outcomes Scale at Day 15, among adults with COVID-19 requiring hospitalization.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
974

participants targeted

Target at P50-P75 for phase_3 covid19

Timeline
Completed

Started Apr 2020

Typical duration for phase_3 covid19

Geographic Reach
1 country

26 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 21, 2020

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 24, 2020

Completed
Same day until next milestone

Study Start

First participant enrolled

April 24, 2020

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 6, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 6, 2021

Completed
1.2 years until next milestone

Results Posted

Study results publicly available

November 3, 2022

Completed
Last Updated

November 3, 2022

Status Verified

October 1, 2022

Enrollment Period

1.2 years

First QC Date

April 21, 2020

Results QC Date

July 6, 2022

Last Update Submit

October 6, 2022

Conditions

Keywords

COVID-19 drug treatmentconvalescent plasma

Outcome Measures

Primary Outcomes (1)

  • COVID-19 7-point Ordinal Clinical Progression Outcomes Scale Score

    Outcome measured clinical status of the participant defined by the Covid-19 7-point Ordinal Clinical Progression Outcomes Scale: This scale reflects a range from baseline to death as follows: 1. Not hospitalized with resumption of normal activities. 2. Not hospitalized, but unable to resume normal activities. 3. Hospitalized, not on supplemental oxygen. 4. Hospitalized, on supplemental oxygen. 5. Hospitalized, on nasal high-flow oxygen therapy, noninvasive mechanical ventilation, or both 6. Hospitalized, on ECMO, invasive mechanical ventilation, or both. 7. Death

    Study Day 15

Secondary Outcomes (11)

  • All-location, All-cause 14-day Mortality

    Baseline to Study Day 14

  • All-location, All-cause 28-day Mortality

    Baseline to Study Day 28

  • Survival Through 28 Days

    Baseline to Day 28 (assessed on Study Day 29)

  • COVID-19 7-point Ordinal Clinical Progression Outcomes Scale on Study Day 3

    Baseline to Study Day 3

  • COVID-19 7-point Ordinal Clinical Progression Outcomes Scale on Study Day 8

    Study Day 8

  • +6 more secondary outcomes

Other Outcomes (8)

  • Acute Kidney Injury

    Baseline to Day 28

  • Renal Replacement Therapy

    Baseline to Day 28

  • Documented Venous Thromboembolic Disease (DVT or PE)

    Baseline to Day 28

  • +5 more other outcomes

Study Arms (2)

pathogen reduced SARS-CoV-2 convalescent plasma

EXPERIMENTAL

Transfusion of convalescent plasma will be administered by clinical or research personnel while the participant is hospitalized on Study Day 0. Plasma will be administered at a rate of 500 mL/hour and will be administered within 12 hours of randomization.

Biological: pathogen reduced SARS-CoV-2 convalescent plasma

Placebo

PLACEBO COMPARATOR

Participants randomized to the control group will receive 250mL of Lactate Ringers containing multivitamins intravenously on Day 1 as a placebo.

Biological: Placebo

Interventions

Convalescent COVID-19 donor plasma is the liquid part of blood that is collected from patients who have recovered from COVID-19 infection. This plasma contains SARS-CoV-2 specific antibodies that may help fight the infection.

pathogen reduced SARS-CoV-2 convalescent plasma
PlaceboBIOLOGICAL

Lactated Ringer's solution with multivitamins

Placebo

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age greater than or equal to 18 years
  • Currently hospitalized or in an emergency department with anticipated hospitalization
  • Symptoms of acute respiratory infection, defined as one or more of the following:
  • Cough
  • Chills, or a fever (greater than 37.5° C or 99.5° F)
  • Shortness of breath, operationalized as a patient having any of the following:
  • i. Subjective shortness of breath reported by a patient or surrogate. ii. Tachypnea with respiratory rate of greater than 22 breaths per minute iii. Hypoxemia, defined as SpO2 less than 92% on room air, new receipt of supplemental oxygen to maintain SpO2 greater than or equal to 92%, or increased supplemental oxygen to maintain SpO2 greater than or equal to 92% for a patient on chronic oxygen therapy
  • Laboratory-confirmed SARS-CoV-2 infection within the past 14 days

You may not qualify if:

  • Prisoner
  • Unable to randomize within 14 days after onset of acute respiratory infection symptoms
  • Patient, legal representative, or physician not committed to full support (Exception: a patient who will receive all supportive care except for attempts at resuscitation from cardiac arrest will not be excluded.)
  • Inability to be contacted on Day 29-36 for clinical outcome assessment
  • Receipt of any SARS-CoV-2 passive immunity therapy, such as convalescent plasma, monoclonal antibodies, or pooled immunoglobulin, in the past 30 days
  • Contraindications to transfusion or history of prior reactions to transfused blood products
  • Plan for hospital discharge within 24 hours of enrollment
  • Previous enrollment in this trial
  • Previous laboratory-confirmed SARS-CoV-2 infection before the current illness
  • Enrollment in another clinical trial evaluating monoclonal antibodies, convalescent plasma, or another passive immunity therapy
  • Prior receipt of SARS-CoV-2 vaccine

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (26)

University of Arkansas for Medical Sciences

Little Rock, Arkansas, 72205, United States

Location

Scripps Health

La Jolla, California, 92037, United States

Location

University of Colorado Denver

Aurora, Colorado, 80045, United States

Location

MedStar Health Research Institute/MedStar Washington Hospital Center

Washington D.C., District of Columbia, 20010, United States

Location

Cleveland Clinic Florida

Weston, Florida, 33331, United States

Location

University of Chicago

Chicago, Illinois, 60637, United States

Location

Loyola University Medical Center

Maywood, Illinois, 60153, United States

Location

The University of Kansas Medical Center

Kansas City, Kansas, 66160, United States

Location

Our Lady of the Lake Regional Medical Center

Baton Rouge, Louisiana, 70808, United States

Location

University of Maryland, Baltimore (University of Maryland Medical Center)

Baltimore, Maryland, 21201, United States

Location

Beth Israel Deaconess Medical Center

Boston, Massachusetts, 02215, United States

Location

Newton-Wellelsey Hospital

Newton, Massachusetts, 012462, United States

Location

University of Minnesota

Minneapolis, Minnesota, 55455, United States

Location

University of Mississippi Medical Center

Jackson, Mississippi, 39216, United States

Location

University of New Mexico Health Sciences Center

Albuquerque, New Mexico, 87131, United States

Location

University at Buffalo/Buffalo General Medical Center

Buffalo, New York, 14203, United States

Location

Rochester General Hospital

Rochester, New York, 14621, United States

Location

Cleveland Clinic Ohio

Cleveland, Ohio, 44195, United States

Location

The Ohio State University Wexner Medical Center and James Cancer Hospital

Columbus, Ohio, 43210, United States

Location

Vanderbilt University Medical Center

Nashville, Tennessee, 37203, United States

Location

Meharry Medical College

Nashville, Tennessee, 37208, United States

Location

Utah Valley Hospital

Provo, Utah, 84604, United States

Location

University of Utah Health

Salt Lake City, Utah, 84132, United States

Location

Sentara Norfolk General Hospital

Norfolk, Virginia, 23507, United States

Location

Virginia Commonwealth University

Richmond, Virginia, 23298, United States

Location

University of Washington

Seattle, Washington, 98104, United States

Location

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  • Self WH, Wheeler AP, Stewart TG, Schrager H, Mallada J, Thomas CB, Cataldo VD, O'Neal HR Jr, Shapiro NI, Higgins C, Ginde AA, Chauhan L, Johnson NJ, Henning DJ, Jaiswal SJ, Mammen MJ, Harris ES, Pannu SR, Laguio-Vila M, El Atrouni W, de Wit M, Hoda D, Cohn CS, McWilliams C, Shanholtz C, Jones AE, Raval JS, Mucha S, Ipe TS, Qiao X, Schrantz SJ, Shenoy A, Fremont RD, Brady EJ, Carnahan RH, Chappell JD, Crowe JE Jr, Denison MR, Gilchuk P, Stevens LJ, Sutton RE, Thomsen I, Yoder SM, Bistran-Hall AJ, Casey JD, Lindsell CJ, Wang L, Pulley JM, Rhoads JP, Bernard GR, Rice TW; Passive Immunity Trial for Our Nation (PassITON) Investigators. Neutralizing COVID-19 Convalescent Plasma in Adults Hospitalized With COVID-19: A Blinded, Randomized, Placebo-Controlled Trial. Chest. 2022 Nov;162(5):982-994. doi: 10.1016/j.chest.2022.06.029. Epub 2022 Jul 1.

  • Self WH, Stewart TG, Wheeler AP, El Atrouni W, Bistran-Hall AJ, Casey JD, Cataldo VD, Chappell JD, Cohn CS, Collins JB, Denison MR, de Wit M, Dixon SL, Duggal A, Edwards TL, Fontaine MJ, Ginde AA, Harkins MS, Harrington T, Harris ES, Hoda D, Ipe TS, Jaiswal SJ, Johnson NJ, Jones AE, Laguio-Vila M, Lindsell CJ, Mallada J, Mammen MJ, Metcalf RA, Middleton EA, Mucha S, O'Neal HR Jr, Pannu SR, Pulley JM, Qiao X, Raval JS, Rhoads JP, Schrager H, Shanholtz C, Shapiro NI, Schrantz SJ, Thomsen I, Vermillion KK, Bernard GR, Rice TW; Passive Immunity Trial for Our Nation (PassITON) Investigators. Passive Immunity Trial for Our Nation (PassITON): study protocol for a randomized placebo-control clinical trial evaluating COVID-19 convalescent plasma in hospitalized adults. Trials. 2021 Mar 20;22(1):221. doi: 10.1186/s13063-021-05171-2.

  • Self WH, Stewart TG, Wheeler AP, El Atrouni W, Bistran-Hall AJ, Casey JD, Cataldo VD, Chappell JD, Cohn CS, Collins JB, Denison MR, de Wit M, Dixon SL, Duggal A, Edwards TL, Fontaine MJ, Ginde AA, Harkins MS, Harrington T, Harris ES, Hoda D, Ipe TS, Jaiswal SJ, Johnson NJ, Jones AE, Laguio-Vila M, Lindsell CJ, Mallada J, Mammen MJ, Metcalf RA, Middleton EA, Mucha S, O'Neal HR, Pannu SR, Pulley JM, Qiao X, Raval JS, Rhoads JP, Schrager H, Shanholtz C, Shapiro NI, Schrantz SJ, Thomsen I, Vermillion KK, Bernard GR, Rice TW. Passive Immunity Trial for Our Nation (PassITON): study protocol for a randomized placebo-control clinical trial evaluating COVID-19 convalescent plasma in hospitalized adults. Res Sq [Preprint]. 2021 Mar 2:rs.3.rs-227796. doi: 10.21203/rs.3.rs-227796/v1.

Related Links

MeSH Terms

Conditions

COVID-19Coronavirus Infections

Condition Hierarchy (Ancestors)

Pneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung DiseasesRespiratory Tract Diseases

Results Point of Contact

Title
Todd Rice, M.D., MSc
Organization
Vanderbilt University Medical Center

Study Officials

  • Todd Rice, MD

    Vanderbilt University Medical Center

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Eligible participants will be randomized 1:1 to convalescent plasma versus lactated Ringer's solution with multivitamins. Randomization will be completed in permuted blocks and stratified by site, gender, and age. Participants, treating clinicians and outcomes assessors will all be blinded to study group assignment. Study personnel will not be blinded to the study group assignment.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Medicine

Study Record Dates

First Submitted

April 21, 2020

First Posted

April 24, 2020

Study Start

April 24, 2020

Primary Completion

July 6, 2021

Study Completion

August 6, 2021

Last Updated

November 3, 2022

Results First Posted

November 3, 2022

Record last verified: 2022-10

Data Sharing

IPD Sharing
Will not share

Locations