Evidence map›Paper›PMID 39455575›Full record

Trial reportNature communications2024

The regulatory T cell-selective interleukin-2 receptor agonist rezpegaldesleukin in the treatment of inflammatory skin diseases: two randomized, double-blind, placebo-controlled phase 1b trials.

Jonathan I Silverberg, David Rosmarin, Raj Chovatiya, Thomas Bieber, Stephen Schleicher, Lisa Beck, Melinda Gooderham, Sohail Chaudhry, Christie Fanton, Danni Yu and 8 more

2 registry-linked trialsAbstract readRandomized Controlled TrialClinical Trial, Phase I
In one paragraph

Trial report in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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.

NCT04081350 phase1completednot on this map

A Phase 1, Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous LY3471851 in Patients With Atopic Dermatitis

TypeinterventionalSponsorNektar TherapeuticsRan2019 to 2022Enrolled48ConditionsDermatitis, AtopicArmsLY3471851, Placebo
NCT04119557 phase1completednot on this map

A Phase 1, Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous LY3471851 in Patients With Psoriasis

TypeinterventionalSponsorNektar TherapeuticsRan2019 to 2021Enrolled30ConditionsPsoriasisArmsPlacebo, LY3471851
3 · Its place in the literature

Who cites it

34 citing papers in PubMed.

  1. Trial
  2. Review
  3. Regulatory T cells: From Foxp3 to tolerance-inducing therapies.The Journal of investigative dermatology · 2026
    Review
  4. Defining the Potential for Disease Modification in Atopic Dermatitis.American journal of clinical dermatology · 2026
    Review
  5. Review
  6. Atopic Dermatitis: New Targets and Emerging Systemic Therapies.American journal of clinical dermatology · 2026
    Review
  7. Review
  8. Article
  9. Selective impact on regulatory T cells with sustained functional phenotypes by the interleukin-2 mutein VIS171 in a nonhuman primate model.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  10. Atopic dermatitis.Nature reviews. Disease primers · 2026
    Review
  11. Bridging Rare to Common Diseases: Precision Medicine and the Transforming Landscape of Pediatric Allergy and Immunology.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Review
  12. Memory Cells in Atopic Dermatitis: Paving the Way to Disease Modification.International journal of molecular sciences · 2026
    Review
  13. Atopic Dermatitis-like mouse model using early inoculation of patient-derivedJID innovations : skin science from molecules to population health · 2026
    Article
  14. Review
  15. Single-CellInternational journal of molecular sciences · 2026
    Article
  16. Article
  17. Review
  18. 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

18 authors.

Jonathan I SilverbergDepartment of Dermatology, George Washington University School of Medicine, Washington, DC, USA.
David RosmarinIndiana University School of Medicine, Indianapolis, IN, USA.
Raj ChovatiyaChicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.ORCID 0000-0001-6510-399X
Thomas BieberDepartment of Dermatology, University Hospital, Zürich, Switzerland.
Stephen SchleicherDermDox Centers for Dermatology, Sugarloaf, PA, USA.
Lisa BeckUniversity of Rochester Medical Center, Rochester, NY, USA.ORCID 0000-0002-8452-667X
Melinda GooderhamDepartment of Medicine, Queen's University, Kingston, ON, Canada.
Sohail ChaudhryNektar Therapeutics, San Francisco, CA, USA.
Christie FantonNektar Therapeutics, San Francisco, CA, USA.
Danni YuNektar Therapeutics, San Francisco, CA, USA.
Joshua LevyLevy Informatics LLC, Chapel Hill, NC, USA.
Yi LiuNektar Therapeutics, San Francisco, CA, USA.
Takahiro MiyazakiNektar Therapeutics, San Francisco, CA, USA.
Mary TagliaferriNektar Therapeutics, San Francisco, CA, USA.
Carsten SchmitzEli Lilly and Company, Indianapolis, IN, USA.
Ajay NirulaRecludix Pharma, San Diego, CA, USA, formerly affiliated with Eli Lilly and Company, Indianapolis, IN, USA.
Brian KotzinNektar Therapeutics, San Francisco, CA, USA.
Jonathan ZalevskyNektar Therapeutics, San Francisco, CA, USA. JZalevsky@nektar.com.ORCID 0000-0003-2707-1709

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cell (Treg) impairment is implicated in the pathogenesis of chronic inflammatory diseases, but relatively little is known about the therapeutic potential of Treg restoration. Here we present clinical evidence for the Treg-selective interleukin-2 receptor agonist rezpegaldesleukin (REZPEG) in two randomized, double-blind, placebo-controlled Phase 1b trials in patients with moderate-to-severe atopic dermatitis (AD) (NCT04081350) or chronic plaque psoriasis (PsO) (NCT04119557). Key inclusion criteria for AD included an Eczema Area and Severity Index (EASI) score ≥ 16 and a validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) ≥ 3, and for PsO included a Psoriasis Area and Severity Index (PASI) score of ≥ 12 and a static Physician's Global Assessment (sPGA) score of ≥ 3. REZPEG is safe and well-tolerated and demonstrates consistent pharmacokinetics in participants receiving subcutaneous doses of 10 to 12 µg/kg or 24 µg/kg once every 2 weeks for 12 weeks, meeting the primary and secondary objectives, respectively. AD patients receiving the higher dose demonstrate an 83% improvement in EASI score after 12 weeks of treatment. EASI improvement of ≥ 75% (EASI-75) and vIGA-AD responses are maintained for 36 weeks after treatment discontinuation in 71% and 80% of week 12 responders, respectively. These exploratory clinical improvements are accompanied by sustained increases in CD25

Indexed as

Dermatitis, AtopicPsoriasisT-Lymphocytes, RegulatoryAdolescentAdultAgedDouble-Blind MethodFemaleHumansMaleMiddle AgedReceptors, Interleukin-2Treatment OutcomeYoung AdultReceptors, Interleukin-2

Identifiers

PMID39455575
PMCPMC11511931

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.