Evidence map›Paper›PMID 37779541›Full record

ArticleThe journal of allergy and clinical immunology. Global2022

IL-33 receptor inhibition in subjects with uncontrolled asthma: A randomized, placebo-controlled trial.

Courtney Crim, Sally Stone, Valerie Millar, Sally Lettis, Elisabeth H Bel, Andrew Menzies-Gow, Pascal Chanez, Sally Wenzel, Njira Lugogo, Eugene R Bleecker

Open access · goldAbstract read
In one paragraph

Article in The journal of allergy and clinical immunology. Global, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  11. New targets for type 2-low asthma.The Korean journal of internal medicine · 2024
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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

10 authors at 7 institutions in 4 countries.

Courtney CrimResearch and Development, GSK, Research Triangle Park, NC.
Sally StoneBiostatistics, GSK, Stockley Park, London, United Kingdom.
Valerie MillarBiostatistics, GSK, Stockley Park, London, United Kingdom.
Sally LettisBiostatistics, GSK, Stockley Park, London, United Kingdom.
Elisabeth H BelDepartment of Respiratory Medicine, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Andrew Menzies-GowDepartment of Respiratory Medicine, Royal Brompton Hospital, London, United Kingdom.
Pascal ChanezDepartment of Respiratory Diseases, C2VN Inserm University of Aix-Marseille, Marseille, France.
Sally WenzelAsthma Institute at University of Pittsburgh Medical Center, Pulmonary Allergy and Critical Care Medicine Division and Department of Environmental and Occupational Health, Pittsburgh, Pa.
Njira LugogoInternal Medicine, Division of Pulmonary, Critical Care Medicine, University of Michigan, Ann Arbor, Mich.
Eugene R BleeckerDepartment of Medicine, University of Arizona, Tucson, Ariz.
Inserm · FRResearch Triangle Park Foundation · USRoyal Brompton Hospital · GBUniversity of Amsterdam · NLUniversity of Arizona · USUniversity of Michigan · USUniversity of Pittsburgh Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Most biologics for severe asthma target only type 2 immunity. Inhibition of IL-33 signaling has the potential to target type 2 and non-type 2 pathways. Objective: This multicenter phase IIA study evaluated the safety and efficacy of GSK3772847, a human mAb directed against the IL-33 receptor (IL-33R) in subjects with moderate-to-severe uncontrolled asthma. Methods: Adults with uncontrolled asthma despite inhaled corticosteroid/long-acting β Results: At week 16, 56 participants (81%) and 45 (66%) receiving placebo and GSK3772847, respectively, had loss of asthma control (an 18% reduction [95% credible interval = 2%-35%]). Early loss of asthma control prevented full analysis of the secondary efficacy end points after week 4. The most frequent classes of treatment-related adverse events were cardiac disorders (n = 3 [4%] in both groups) and musculoskeletal/connective tissue disorders (with GSK3772847, n = 3 [4%]; with placebo n = 0). Target engagement of IL-33R by GSK3772847 was demonstrated. Conclusion: Treatment with GSK3772847 may be beneficial for patients with uncontrolled asthma. Further studies are warranted.

Indexed as

AsthmaGSK37772847IL-1 receptor-like 1 proteinIL-33mAbplacebo-controlled trialrandomized trial

Identifiers

PMID37779541
PMCPMC10509964
OpenAlexW4292324093

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.