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Reducing COVID-19 Related Hospital Admission in Elderly by BCG Vaccination

Primary Purpose

COVID-19

Status
Unknown status
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
BCG vaccine
Placebo
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for COVID-19 focused on measuring BCG, Bacille Calmette-Guérin, COVID-19, SARS-CoV-2, trained immunity, off-target effects

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adult (≥ 60 years)

Exclusion Criteria:

  • Fever (>38 ºC) within the past 24 hours
  • Suspicion of current active viral or bacterial infection
  • Expected vaccination during the first three months of the study period
  • Severely immunocompromised subjects. This exclusion category comprises: a) subjects with known infection by the human immunodeficiency virus (HIV-1); b) neutropenic subjects with less than 500 neutrophils/mm3; c) subjects with solid organ transplantation; d) subjects with bone marrow transplantation; e) subjects under chemotherapy; f) subjects with primary immunodeficiency; g) severe lymphopenia with less than 400 lymphocytes/mm3; h) treatment with any immunosuppressant drugs such as anti-cytokine therapies, and treatment with oral or intravenous steroids defined as daily doses of 10mg prednisone or equivalent for longer than 3 months, or probable use of oral or intravenous steroids in the following four weeks.
  • Active solid or non-solid malignancy or lymphoma within the prior two years
  • Active participation in another research study that involves BCG administration

Sites / Locations

  • Radboud University
  • UMC Utrecht

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Treatment

Placebo

Arm Description

BCG vaccine (Danish strain 1331, SSI, Denmark)

0.9% NaCl

Outcomes

Primary Outcome Measures

SARS-CoV-2 related hospital admission

Secondary Outcome Measures

the duration of hospital admission due to documented COVID-19
the cumulative incidence of documented SARS-CoV-2 infection
the cumulative incidence of self-reported acute respiratory symptoms or fever
the cumulative incidence of death due to documented SARS-CoV-2 infection
the cumulative incidence of hospital admission for any reason
the cumulative incidence of Intensive Care Admission due to documented SARS-CoV-2 infection

Full Information

First Posted
May 25, 2020
Last Updated
June 3, 2020
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04417335
Brief Title
Reducing COVID-19 Related Hospital Admission in Elderly by BCG Vaccination
Official Title
Reducing Hospital Admission of Elderly in SARS-CoV-2 Pandemic Via the Induction of Trained Immunity by Bacillus Calmette-Guérin Vaccination, a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 16, 2020 (Actual)
Primary Completion Date
May 2021 (Anticipated)
Study Completion Date
May 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bacillus Calmette-Guérin (BCG) vaccine not only protects against tuberculosis, but has also been shown to induce protection against various infections with a viral aetiology, leading to significant reductions in morbidity and mortality. We hypothesize that BCG vaccination might be a potent preventive measure against SARS-CoV-2 infection and/or may reduce disease severity in elderly people, who are known to be at increased risk of illness and death from SARS-CoV-2 infection. Therefore, we will in this placebo-controlled adaptive multi-centre randomized controlled trial evaluate the ability of BCG to reduce hospital admission and its efficacy to improve the clinical course of SARS-CoV-2 infection in elderly people((≥ 60 years of age).
Detailed Description
On March 11 2020 the World Health Organization (WHO) declared the coronavirus (SARS-CoV-2) outbreak a pandemic. The number of confirmed cases continues to rise, leading to significant morbidity and mortality worldwide. Although individuals of any age can acquire SARS-CoV-2, adults of middle age and older are most commonly affected. Moreover, recent reports demonstrate that mortality rates rise significantly among patients 60 years and older. Therefore, strategies to prevent SARS-CoV-2 infection or to reduce its clinical consequences in elderly are desperately needed. Bacillus Calmette-Guérin (BCG) vaccine not only protects against tuberculosis, but has also been shown to induce protection against various infections with a viral aetiology, leading to significant reductions in morbidity and mortality. We hypothesize that BCG vaccination may reduce hospital admission and improve the clinical course of symptoms of elderly people during the SARS-CoV-2 outbreak. Primary objective: To reduce hospital admission of community dwelling older persons during the pandemic of SARS-CoV-2. Secondary objective: To reduce disease severity, the duration of hospital admission, ICU admission, or death in elderly during the pandemic of SARS-CoV-2. Study design: A placebo-controlled adaptive multi-centre randomized controlled trial. Study population: Elderly people (≥ 60 years of age). Intervention: Participants will be randomized between intracutaneous administration of BCG vaccine or placebo in a 1:1 ratio.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
Keywords
BCG, Bacille Calmette-Guérin, COVID-19, SARS-CoV-2, trained immunity, off-target effects

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
placebo-controlled adaptive multi-centre randomized controlled trial
Masking
Participant
Allocation
Randomized
Enrollment
2014 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
BCG vaccine (Danish strain 1331, SSI, Denmark)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
0.9% NaCl
Intervention Type
Biological
Intervention Name(s)
BCG vaccine
Intervention Description
Bacille Calmette-Guérin is a live attenuated strain of Mycobacterium bovis developed in 1921 to prevent tuberculosis and other mycobacterial related infections.
Intervention Type
Biological
Intervention Name(s)
Placebo
Intervention Description
0.9% NaCl
Primary Outcome Measure Information:
Title
SARS-CoV-2 related hospital admission
Time Frame
Maximum of 1 year
Secondary Outcome Measure Information:
Title
the duration of hospital admission due to documented COVID-19
Time Frame
Maximum of 1 year
Title
the cumulative incidence of documented SARS-CoV-2 infection
Time Frame
Maximum of 1 year
Title
the cumulative incidence of self-reported acute respiratory symptoms or fever
Time Frame
Maximum of 1 year
Title
the cumulative incidence of death due to documented SARS-CoV-2 infection
Time Frame
1 year
Title
the cumulative incidence of hospital admission for any reason
Time Frame
Maximum of 1 year
Title
the cumulative incidence of Intensive Care Admission due to documented SARS-CoV-2 infection
Time Frame
Maximum of 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adult (≥ 60 years) Exclusion Criteria: Fever (>38 ºC) within the past 24 hours Suspicion of current active viral or bacterial infection Expected vaccination during the first three months of the study period Severely immunocompromised subjects. This exclusion category comprises: a) subjects with known infection by the human immunodeficiency virus (HIV-1); b) neutropenic subjects with less than 500 neutrophils/mm3; c) subjects with solid organ transplantation; d) subjects with bone marrow transplantation; e) subjects under chemotherapy; f) subjects with primary immunodeficiency; g) severe lymphopenia with less than 400 lymphocytes/mm3; h) treatment with any immunosuppressant drugs such as anti-cytokine therapies, and treatment with oral or intravenous steroids defined as daily doses of 10mg prednisone or equivalent for longer than 3 months, or probable use of oral or intravenous steroids in the following four weeks. Active solid or non-solid malignancy or lymphoma within the prior two years Active participation in another research study that involves BCG administration
Facility Information:
Facility Name
Radboud University
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525 GA
Country
Netherlands
Facility Name
UMC Utrecht
City
Utrecht
ZIP/Postal Code
3584 CX
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35247264
Citation
Moorlag SJCFM, Taks E, Ten Doesschate T, van der Vaart TW, Janssen AB, Muller L, Ostermann P, Dijkstra H, Lemmers H, Simonetti E, Mazur M, Schaal H, Ter Heine R, van de Veerdonk FL, Bleeker-Rovers CP, van Crevel R, Ten Oever J, de Jonge MI, Bonten MJ, van Werkhoven CH, Netea MG. Efficacy of BCG Vaccination Against Respiratory Tract Infections in Older Adults During the Coronavirus Disease 2019 Pandemic. Clin Infect Dis. 2022 Aug 24;75(1):e938-e946. doi: 10.1093/cid/ciac182.
Results Reference
derived

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Reducing COVID-19 Related Hospital Admission in Elderly by BCG Vaccination

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