Evidence map›Paper›PMID 39563457›Full record

ArticleTrials2024

A phase 1 randomized controlled trial of a peptide-based group A streptococcal vaccine in healthy volunteers.

Vanessa Meier-Stephenson, Michael T Hawkes, Catherine Burton, Ainslie Calcutt, Chris Davis, Jessica Dooley, Michael Good, Michael Houghton, Eloise Keeffe, Kelly Kim and 13 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04882514 (A Randomized Double Blinded Within Dose, Controlled, Safety and Immunogenicity Study of GAS Vaccine Candidate in Healthy Individuals.), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04882514 phase1 / phase2completednot on this map

A Randomized Double Blinded Within Dose, Controlled, Safety and Immunogenicity Study of GAS Vaccine Candidate in Healthy Individuals.

TypeinterventionalSponsorUniversity of AlbertaRan2022 to 2025Enrolled30ConditionsGroup A Streptococcal InfectionArmsp*17-K4S2, J8-K4S2, Rabavert vaccine
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. [Use of vaccines to prevent the development of bacterial resistance].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2026
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  5. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Vanessa Meier-Stephenson *Department of Medicine/Division of Infectious Diseases, University of Alberta, Edmonton, AB, Canada. meierste@ualberta.ca.ORCID http://orcid.org/0000-0003-4004-4940
Michael T Hawkes *Li Ka Shing Institute of Virology, University of Alberta, Edmonton, AB, Canada.
Catherine BurtonDepartment of Pediatrics, University of Alberta, Edmonton, AB, Canada.
Ainslie CalcuttLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Chris DavisLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Jessica DooleyLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Michael GoodDepartment of Medical Microbiology and Immunology, University of Alberta, Edmonton, AB, Canada.
Michael HoughtonLi Ka Shing Institute of Virology, University of Alberta, Edmonton, AB, Canada.
Eloise KeeffeLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Kelly KimClinical Trials Office, University of Alberta, Edmonton, AB, Canada.
Ailin LepletierLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Conar O'NeilDepartment of Medicine/Division of Infectious Diseases, University of Alberta, Edmonton, AB, Canada.
Ijeoma OgbuehiClinical Trials Office, University of Alberta, Edmonton, AB, Canada.
Victoria OzberkLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Manisha PandeyLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Simone ReynoldsLaboratory of Vaccines for the Developing World, Institute for Biomedicine and Glycomics, Griffith University, Nathan, QLD, Australia.
Avi SethClinical Trials Office, University of Alberta, Edmonton, AB, Canada.
William StokesDepartment of Medicine/Division of Infectious Diseases, University of Alberta, Edmonton, AB, Canada.
Alena Tse-ChangDepartment of Pediatrics, University of Alberta, Edmonton, AB, Canada.
Ben TyrrellDepartment of Medicine/Division of Cardiology, University of Alberta, Edmonton, Canada.
D Lorne TyrrellLi Ka Shing Institute of Virology, University of Alberta, Edmonton, AB, Canada.
Gregory J TyrrellDepartment Laboratory Medicine & Pathology, University of Alberta, Edmonton, AB, Canada.
Maryna YaskinaFaculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGroup A streptococci (Strep A) orStreptococcus pyogenes is a major human pathogen causing an estimated 500,000 deaths worldwide each year. Disease can range from mild pharyngitis to more severe infections, such as necrotizing fasciitis, septicemia, and toxic shock syndrome. Untreated, Strep A infection can lead to the serious post streptococcal pathologies of rheumatic fever/rheumatic heart disease and post-streptococcal glomerulonephritis. An effective vaccine against Strep A would have great benefits worldwide. Here, we test two products, J8 and p*17-both peptide derivatives of a highly conserved region in the M protein, in combination with the protein subunit K4S2 of SpyCEP, an IL-8 protease associated with neutrophil chemoattraction. Each peptide is individually conjugated to cross reacting material (CRM

methodsThis single-site phase I, two-stage clinical trial in Edmonton, Alberta, Canada, aims to recruit a total of 30 healthy volunteers, aged 18-45 years, without any evidence of pre-existing valvular heart disease. The trial is divided into the initial unblinded safety test dose stage (stage 1) and the randomized, double-blinded, controlled trial stage (stage 2). Stage 1 will recruit 10 volunteers-5 each to receive either J8-K4S2 or p*17-K4S2 in an unblinded, staggered fashion, whereby volunteers are dosed with intentional spacing of at least 2 days in between doses to monitor for any immediate side effects before dosing the next. Once all 5 volunteers have received 3 doses of the first test vaccine, a similar process will follow for the second test vaccine. Once safety is established in stage 1, we will proceed to stage 2, which will recruit 20 volunteers to our 3-arm randomized controlled trial (RCT), receiving either of the trial vaccines, J8-K4S2 or p*17-K4S2, or comparator (rabies) vaccine. All product dosing will be at 0, 3, and 6 weeks. The primary outcome is vaccine safety; the secondary outcome is immunogenicity and comparative analyses of the different vaccine regimens. DISCUSSION: This Strep A vaccine clinical trial aims to investigate safety and immunogenicity of two novel conjugated peptide-based vaccines, J8-KS42 and p*17-K4S2. If one or both vaccine products demonstrate favorable primary and secondary outcomes, the product(s) will move into phase II and III studies.

trial registrationClinicalTrials.gov Identifier: NCT04882514. Registered on 2021-05-12, https://clinicaltrials.gov/study/NCT04882514 .

Indexed as

Streptococcal VaccinesStreptococcus pyogenesVaccines, SubunitAdolescentAdultAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsCarrier ProteinsClinical Trials, Phase I as TopicDouble-Blind MethodFemaleHealthy VolunteersHumansImmunogenicity, VaccineMaleAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsCarrier Proteinsstreptococcal M proteinStreptococcal VaccinesVaccines, SubunitGroup A streptococcus (GAS; Strep a)M proteinPhase I vaccine clinical trialSpy-CEPStreptococcus pyogenes

Identifiers

PMID39563457
PMCPMC11577953

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.