Evidence map›Paper›PMID 31049972›Full record

Trial reportAllergy2019

The clinical benefit of mepolizumab replacing omalizumab in uncontrolled severe eosinophilic asthma.

Kenneth R Chapman, Frank C Albers, Bradley Chipps, Xavier Muñoz, Gilles Devouassoux, Miguel Bergna, Dmitry Galkin, Jay Azmi, Dalal Mouneimne, Robert G Price and 1 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Allergy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 3 pooled it
10.8field-weighted citation impact, top 1% of its field
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

77 citing papers in PubMed, 3 syntheses or guidelines pooled it, 157 citations in OpenAlex.

  1. Pooled it
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  8. Comparative effectiveness of mepolizumab and omalizumab in patients eligible for both: a retrospective cohort study.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2026
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  17. Improving patient outcomes: Mepolizumab's impact in IL-5-mediated diseases.Lung India : official organ of Indian Chest Society · 2025
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17 more citing papers are in PubMed but not listed here.

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

11 authors at 10 institutions in 7 countries.

Kenneth R ChapmanAsthma and Airway Centre, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Frank C AlbersGlobal Respiratory Medical Franchise, GSK, Research Triangle Park, North Carolina.ORCID 0000-0001-7039-4621
Bradley ChippsCapital Allergy and Respiratory Disease Center, Sacramento, California.
Xavier MuñozPulmonology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Gilles DevouassouxService de Pneumologie, Hôpital de la Croix Rousse, Hospices Civils de Lyon, UCB Lyon 1, Lyon, France.
Miguel BergnaRespiratory Research, CEMER, Vicente Lopez, Buenos Aires, Argentina.
Dmitry GalkinGlobal Respiratory Medical Franchise, GSK, Research Triangle Park, North Carolina.
Jay AzmiRespiratory TAU, GSK, Uxbridge, UK.
Dalal MouneimneGlobal Medical Affairs, GSK House, Brentford, Middlesex, UK.
Robert G PriceClinical Statistics, GSK, Stevenage, UK.
Mark C LiuDivisions of Allergy and Clinical Immunology, Pulmonary and Critical Care Medicine, Johns Hopkins Asthma and Allergy Center, Baltimore, Maryland.
Research Triangle Park Foundation · USAge UK · GBBrunel University of London · GBCapital Allergy and Respiratory Disease Center · USCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESGlaxoSmithKline (Germany) · DENational Institute of Industrial Technology · ARPulmonary and Allergy Associates · USUniversité Claude Bernard Lyon 1 · FRUniversity Health Network · CA

Funding

GlaxoSmithKline 204471
6 · The paper itself

Abstract

backgroundMepolizumab and omalizumab are treatments for distinct but overlapping severe asthma phenotypes.

objectiveTo assess if patients eligible for both biologics but not optimally controlled with omalizumab experience improved asthma control when switched directly to mepolizumab.

methodsOSMO was a multicenter, open-label, single-arm, 32-week trial in patients with ≥2 asthma exacerbations in the year prior to enrollment, despite receiving high-dose inhaled corticosteroids and other controller(s), plus omalizumab (≥4 months). At baseline, patients with blood eosinophil counts ≥150 cells/µL (or ≥300 cells/µL in the prior year) and an Asthma Control Questionnaire (ACQ)-5 score ≥1.5 discontinued omalizumab and immediately commenced mepolizumab 100 mg subcutaneously every 4 weeks. Endpoints included change from baseline in ACQ-5 score (primary), St George's Respiratory Questionnaire (SGRQ) score and the proportions of ACQ-5 and SGRQ responders, all at Week 32, and the annualized exacerbation rate over the study period.

resultsAt Week 32 (intent-to-treat population [n = 145]), the least squares (LS) mean changes (standard error [SE]) in ACQ-5 and SGRQ total scores were -1.45 (0.107) and -19.0 (1.64) points; with 77% and 79% of patients achieving the minimum clinically important differences (ACQ-5: ≥0.5 points; SGRQ: ≥4 points), respectively. The annualized rate of clinically significant exacerbations was 1.18 events/year, a 64% reduction from 3.26 events/year during the previous year. Safety and immunogenicity profiles were consistent with previous trials.

conclusionAfter directly switching from omalizumab to mepolizumab, patients with uncontrolled severe eosinophilic asthma experienced clinically significant improvements in asthma control, health status, and exacerbation rate, with no tolerability issues reported.

Indexed as

Drug SubstitutionAdolescentAdultAgedAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedAsthmaChildEosinophilsFemaleHumansLeukocyte CountMaleMiddle AgedOmalizumabQuality of LifeAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedmepolizumabOmalizumabACQ-5asthma controlmepolizumabomalizumabsevere eosinophilic asthma

Identifiers

PMID31049972
PMCPMC6790683
OpenAlexW2943295610

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.