Evidence map›Paper›PMID 39060015›Full record

Trial reportThe European respiratory journal2024

Benralizumab for allergic asthma: a randomised, double-blind, placebo-controlled trial.

Gail M Gauvreau, Roma Sehmi, J Mark FitzGerald, Richard Leigh, Donald W Cockcroft, Beth E Davis, Irvin Mayers, Louis-Philippe Boulet, Dhuha Al-Sajee, Brittany M Salter and 18 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The European respiratory journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Rethinking asthma therapy, part 2: transdermal strategies for adjunct asthma and allergy treatments.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Predicting airway hyperresponsiveness to methacholine in patients with atopic dermatitis.The journal of allergy and clinical immunology. Global · 2025
    Article
  11. Review
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Gail M GauvreauFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada gauvreau@mcmaster.ca.ORCID https://orcid.org/0000-0002-6187-2385
Roma SehmiFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.ORCID https://orcid.org/0000-0003-0968-6304
J Mark FitzGeraldVancouver General Hospital and University of British Columbia, Vancouver, BC, Canada.
Richard LeighCumming School of Medicine, Calgary, AB, Canada.ORCID https://orcid.org/0009-0007-8959-2899
Donald W CockcroftUniversity of Saskatchewan, Saskatoon, SK, Canada.
Beth E DavisUniversity of Saskatchewan, Saskatoon, SK, Canada.
Irvin MayersUniversity of Alberta, Edmonton, AB, Canada.
Louis-Philippe BouletInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University, Québec City, QC, Canada.
Dhuha Al-SajeeFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Brittany M SalterFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Ruth P CusackFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Terence HoFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.ORCID https://orcid.org/0000-0002-0412-6538
Christiane E WhetstoneFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Nadia AlsajiFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Imran SatiaFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.ORCID https://orcid.org/0000-0003-4206-6000
Kieran J KillianFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Patrick D MitchellTrinity College, Dublin, Ireland.ORCID https://orcid.org/0000-0001-5705-9618
Iain P MageeUniversity of Saskatchewan, Saskatoon, SK, Canada.
Celine BergeronVancouver General Hospital and University of British Columbia, Vancouver, BC, Canada.
Mohit BhutaniUniversity of Alberta, Edmonton, AB, Canada.
Viktoria WerkströmAstraZeneca, Gothenburg, Sweden.
Tomasz DurżyńskiAstraZeneca, Warsaw, Poland.
Kathryn ShoemakerAstraZeneca, Gaithersburg, MD, USA.
Rohit K KatialAstraZeneca, Denver, CO, USA.
Maria JisonAstraZeneca, Gaithersburg, MD, USA.
Paul NewboldAstraZeneca, Gaithersburg, MD, USA.
Christopher McCraeAstraZeneca, Warsaw, Poland.
Paul M O'ByrneFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.ORCID https://orcid.org/0000-0003-0979-281X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBenralizumab induces rapid and near-complete depletion of eosinophils from blood and lung tissue. We investigated whether benralizumab could attenuate the allergen-induced late asthmatic response (LAR) in participants with allergic asthma.

methodsParticipants with allergic asthma who demonstrated increased sputum eosinophils and LAR at screening were randomised to benralizumab 30 mg or matched placebo given every 4 weeks for 8 weeks (3 doses). Allergen challenges were performed at weeks 9 and 12 when blood, sputum, bone marrow and bronchial tissue eosinophils and LAR were assessed.

results46 participants (mean age 30.9 years) were randomised to benralizumab (n=23) or placebo (n=23). Eosinophils were significantly reduced in the benralizumab group compared with placebo in blood at 4 weeks and sputum and bone marrow at 9 weeks after treatment initiation. At 7 h after an allergen challenge at week 9, sputum eosinophilia was significantly attenuated in the benralizumab group compared to placebo (least squares mean difference -5.81%, 95% CI -10.69- -0.94%; p=0.021); however, the LAR was not significantly different (least squares mean difference 2.54%, 95% CI 3.05-8.12%; p=0.363). Adverse events were reported for seven (30.4%) and 14 (60.9%) participants in the benralizumab and placebo groups, respectively.

conclusionBenralizumab administration over 8 weeks resulted in a significant attenuation of blood, bone marrow and sputum eosinophilia in participants with mild allergic asthma; however, there was no change in the LAR, suggesting that eosinophils alone are not a key component of allergen-induced bronchoconstriction.

Indexed as

Anti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedAsthmaEosinophilsSputumAdultAllergensDouble-Blind MethodEosinophiliaFemaleHumansMaleMiddle AgedTreatment OutcomeYoung AdultAllergensAnti-Asthmatic AgentsAntibodies, Monoclonal, Humanizedbenralizumab

Identifiers

PMID39060015
PMCPMC11391094

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Registered trials

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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.