Evidence map›Paper›PMID 36041655›Full record

Trial reportThe Journal of allergy and clinical immunology2022

Phase 2 randomized clinical trial of astegolimab in patients with moderate to severe atopic dermatitis.

Marcus Maurer, Dorothy S Cheung, Wiebke Theess, Xiaoying Yang, Michael Dolton, Anna Guttman, David F Choy, Ajit Dash, Michele A Grimbaldeston, Weily Soong

Abstract readRandomized Controlled TrialClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
11.2field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Atopic Dermatitis: New Targets and Emerging Systemic Therapies.American journal of clinical dermatology · 2026
    Review
  5. Review
  6. Article
  7. Atopic dermatitis.Nature reviews. Disease primers · 2026
    Review
  8. Review
  9. Review
  10. Emerging Systemic Treatments for Asthma and Allergic Diseases: New Tricks, Same Dog?The journal of allergy and clinical immunology. In practice · 2026
    Review
  11. Article
  12. Review
  13. Review
  14. From Pathways to Patients in Atopic Dermatitis: Advanced Systemic Therapies.International journal of molecular sciences · 2025
    Review
  15. Review
  16. IL-31/33 Axis in Atopic Dermatitis.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Review
  19. Review
  20. Targeting alarmins in asthma: From bench to clinic.The Journal of allergy and clinical immunology · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Marcus MaurerFraunhofer Institute for Translational Medicine and Pharmacology, Allergology and Immunology, Berlin, Germany; Institute of Allergology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany. Electronic address: marcus.maurer@charite.de.
Dorothy S CheungGenentech, Inc, South San Francisco, Calif.
Wiebke TheessF Hoffmann-LaRoche, Basel, Switzerland.
Xiaoying YangGenentech, Inc, South San Francisco, Calif.
Michael DoltonRoche Products Australia, Millers Point, Australia.
Anna GuttmanGenentech, Inc, South San Francisco, Calif.
David F ChoyGenentech, Inc, South San Francisco, Calif.
Ajit DashGenentech, Inc, South San Francisco, Calif.
Michele A GrimbaldestonGenentech, Inc, South San Francisco, Calif.
Weily SoongAlabama Allergy and Asthma Center and Clinical Research Center of Alabama, Birmingham, Ala.
Allergy, Asthma and Clinical Research Center · USHumboldt-Universität zu Berlin · DERoche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe binding of IL-33 to its receptor ST2 (alias of IL1RL1) leads to the release of inflammatory mediators and may play a role in the pathogenesis of atopic dermatitis. Astegolimab is a fully human, IgG

objectivesThis study sought to assess the efficacy, safety, and pharmacokinetics of astegolimab in patients with atopic dermatitis.

methodsThis was a randomized, placebo-controlled, phase 2 study in which adults with chronic atopic dermatitis were randomized 1:1 to receive astegolimab 490 mg every 4 weeks or placebo, for 16 weeks. The primary outcome was the percentage of change from baseline to week 16 of the Eczema Area and Severity Index score.

resultsA total of 65 patients were enrolled in the study (placebo, n = 32; astegolimab, n = 33). The adjusted mean percentage of change from baseline to week 16 in the Eczema Area and Severity Index score was -51.47% for astegolimab compared with -58.24% for placebo, with a nonsignificant treatment difference of 6.77% (95% CI: -16.57-30.11; P = .5624). No differences were observed between treatment groups for secondary efficacy outcomes and in exploratory biomarkers (blood eosinophils, serum IL-5, serum CCL13). With the use of loading dose, pharmacokinetic exposure was sufficient from week 1. Astegolimab was well-tolerated, with a safety profile consistent with that observed in previous clinical trials.

conclusionsIn patients with atopic dermatitis, astegolimab did not show a significant difference compared to placebo for the primary or secondary outcomes.

Indexed as

Antibodies, Monoclonal, HumanizedDermatitis, AtopicHumansInterleukin-33Antibodies, Monoclonal, HumanizedastegolimabInterleukin-33Atopic dermatitisIL-33ST2

Identifiers

PMID36041655
OpenAlexW4293331135

What OpenQuestion holds

Textmetadata
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.