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.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
25 Oct 2024
Historique:
received: 16 05 2024
accepted: 08 10 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 25 10 2024
Statut: epublish

Résumé

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

Identifiants

pubmed: 39455575
doi: 10.1038/s41467-024-53384-1
pii: 10.1038/s41467-024-53384-1
doi:

Substances chimiques

Receptors, Interleukin-2 0

Types de publication

Journal Article Randomized Controlled Trial Clinical Trial, Phase I

Langues

eng

Sous-ensembles de citation

IM

Pagination

9230

Informations de copyright

© 2024. The Author(s).

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Auteurs

Jonathan I Silverberg (JI)

Department of Dermatology, George Washington University School of Medicine, Washington, DC, USA.

David Rosmarin (D)

Indiana University School of Medicine, Indianapolis, IN, USA.

Raj Chovatiya (R)

Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Center for Medical Dermatology + Immunology Research, Chicago, IL, USA.

Thomas Bieber (T)

Department of Dermatology, University Hospital, Zürich, Switzerland.
Medicine Campus, Davos, Switzerland.

Stephen Schleicher (S)

DermDox Centers for Dermatology, Sugarloaf, PA, USA.

Lisa Beck (L)

University of Rochester Medical Center, Rochester, NY, USA.

Melinda Gooderham (M)

Department of Medicine, Queen's University, Kingston, ON, Canada.

Sohail Chaudhry (S)

Nektar Therapeutics, San Francisco, CA, USA.

Christie Fanton (C)

Nektar Therapeutics, San Francisco, CA, USA.

Danni Yu (D)

Nektar Therapeutics, San Francisco, CA, USA.

Joshua Levy (J)

Levy Informatics LLC, Chapel Hill, NC, USA.

Yi Liu (Y)

Nektar Therapeutics, San Francisco, CA, USA.

Takahiro Miyazaki (T)

Nektar Therapeutics, San Francisco, CA, USA.

Mary Tagliaferri (M)

Nektar Therapeutics, San Francisco, CA, USA.

Carsten Schmitz (C)

Eli Lilly and Company, Indianapolis, IN, USA.

Ajay Nirula (A)

Recludix Pharma, San Diego, CA, USA, formerly affiliated with Eli Lilly and Company, Indianapolis, IN, USA.

Brian Kotzin (B)

Nektar Therapeutics, San Francisco, CA, USA.

Jonathan Zalevsky (J)

Nektar Therapeutics, San Francisco, CA, USA. JZalevsky@nektar.com.

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