Evidence map›Paper›PMID 38187863›Full record

ArticleThe journal of allergy and clinical immunology. Global2024

Phase 2b randomized trial of OX40 inhibitor telazorlimab for moderate-to-severe atopic dermatitis.

Barbara Rewerska, Lawrence D Sher, Sady Alpizar, Sylvia Pauser, Grazyna Pulka, Neelufar Mozaffarian, Yacine Salhi, Camille Martinet, Wafaa Jabert, Girish Gudi and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in The journal of allergy and clinical immunology. Global, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03568162 (A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of ISB 830 in Adult Subjects With Moderate to Severe Atopic Dermatitis.), which is not on this map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
11.7field-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.

NCT03568162 phase2completednot on this map

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of ISB 830 in Adult Subjects With Moderate to Severe Atopic Dermatitis.

TypeinterventionalSponsorIchnos Sciences SARan2018 to 2021Enrolled462ConditionsModerate to Severe Atopic DermatitisArmsISB 830 - Part 1 Group 1, ISB 830 - Part 1 Group 2, ISB 830 - Part 1 Group 3, Placebo - Part 1 Group 4, ISB 830 - Part 2 Group 5
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Atopic Dermatitis: New Targets and Emerging Systemic Therapies.American journal of clinical dermatology · 2026
    Review
  4. OX40/OX40L modulation: A target for regulating T cells in cutaneous inflammatory disorders.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Review
  5. Review
  6. Review
  7. The Role of OX40 Pathway Inhibition as a New Therapeutic Strategy for Atopic Dermatitis.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. From Pathways to Patients in Atopic Dermatitis: Advanced Systemic Therapies.International journal of molecular sciences · 2025
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Type 2 Inflammation and Its Role in Dermatologic Diseases.International journal of dermatology · 2025
    Review
  19. Review
  20. Article
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

19 authors at 5 institutions in 4 countries.

Barbara RewerskaDiamond Clinic, Krakow, Poland.
Lawrence D SherPeninsula Research Associates, Rolling Hills Estates, Calif.
Sady AlpizarClinical Research Trials of Florida Inc, Tampa, Fla.
Sylvia PauserKliFOs-Klinische Forschung Osnabrück, Osnabrück, Germany.
Grazyna PulkaSchool of Medicine, Jagiellonian University Medical College, Krakow, Poland.
Neelufar MozaffarianIchnos Sciences, New York, NY.
Yacine SalhiIchnos Sciences, New York, NY.
Camille MartinetKeyrus Life Science, Levallois-Perret, France.
Wafaa JabertIchnos Sciences, New York, NY.
Girish GudiIchnos Sciences, New York, NY.
Vinu CaIchnos Sciences, New York, NY.
Sunitha GnGlenmark Pharmaceuticals, Mumbai, India.
Julie MacoinIchnos Sciences, New York, NY.
Victor AnstettIchnos Sciences, New York, NY.
Riccardo TurriniIchnos Sciences, New York, NY.
Marie-Agnès DouceyIchnos Sciences, New York, NY.
Stanislas BleinIchnos Sciences, New York, NY.
Cyril KontoIchnos Sciences, New York, NY.
Martina MachkovaCCR Prague sro, Prague, Czech Republic.
Ichnos Sciences (United States) · USHoneywell (France) · FRJagiellonian University · PLKrakow Cardiovascular Research Institute · PLPeninsula Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Telazorlimab is a humanized anti-OX40 monoclonal antibody being studied for treatment of T-cell-mediated diseases. Objective: This randomized, placebo-controlled, phase 2b dose-range finding study investigated efficacy, safety, pharmacokinetics, and immunogenicity of telazorlimab in subjects with atopic dermatitis. Methods: In this 2-part study (NCT03568162), adults (≥18 years) with moderate-to-severe disease were randomized to various regimens of subcutaneous telazorlimab or placebo for 16 weeks' blinded treatment, followed by 38 weeks' open-label treatment and 12 weeks' drug-free follow-up. Telazorlimab treatment groups (following a loading dose) in part 1 were 300 mg every 2 weeks; 300 mg every 4 weeks; or 75 mg every 4 weeks. Part 2 evaluated telazorlimab 600 mg every 2 weeks. The primary end point was percentage change from baseline in Eczema Area and Severity Index (EASI) at week 16. Safety assessments included incidence of treatment-emergent adverse events. Results: The study randomized 313 subjects in part 1 and 149 in part 2. At 16 weeks, the least squares mean percentage change from baseline in EASI was significantly greater in subjects receiving telazorlimab 300 mg every 2 weeks (part 1) and 600 mg every 2 weeks (part 2) versus placebo (-54.4% vs -34.2% for part 1 and -59.0% vs -41.8% for part 2, Conclusion: Telazorlimab, administered subcutaneously at 300 mg every 2 weeks or 600 mg every 2 weeks following a loading dose, was well tolerated and induced significant and progressive clinical improvement in adults with moderate-to-severe atopic dermatitis.

Indexed as

anti-OX40 receptorAtopic dermatitishumanized monoclonal antibodyphase 2telazorlimab

Identifiers

PMID38187863
PMCPMC10770725
OpenAlexW4388915211

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.