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J Derm TreatRCT

Early response to ivarmacitinib and its impact on long-term efficacy in patients with moderate-to-severe atopic dermatitis

a post hoc analysis of a phase-III trial.

Chen J, Hu F, Zhang P, Chen L

Journal of Dermatological TreatmentIn the feed 15 Jul 2026, published online 15 Jul 2026, issue 2026 Dec, added to PubMed 15 Jul 2026

Topics: Atopic dermatitis & eczemaJAK inhibitors & other targeted pills

Abstract

BACKGROUNDIvarmacitinib, also known as SHR0302, is a novel highly selective Janus kinase 1 inhibitor that suppresses cytokine signaling pathways involved in the pathogenesis of atopic dermatitis (AD).

OBJECTIVEWe aimed to explore the early response to ivarmacitinib in patients with moderate-to-severe AD and its impact on long-term efficacy.

METHODSThis post hoc analysis included all patients receiving ivarmacitinib in the phase-III trial (NCT04875169). Patients were divided into early and nonearly responders, depending on whether they achieved an Eczema Area and Severity Index (EASI) 75 response at week (W) 4.

RESULTSAmong the 225 patients included, 83 (36.9%) were classified as early responders and 142 (63.1%) as nonearly responders. The EASI 75 (81.9% vs. 47.2%, p < 0.001) and Investigator's Global Assessment (IGA) (56.6% vs. 28.9%, p < 0.001) response rates at W16 were higher in early responders. Additionally, early responders had higher EASI 90, EASI 100, and Scoring Atopic Dermatitis 75 and 90 response rates throughout W8 to W52. The changes in Dermatology Life Quality Index and Patient-Oriented Eczema Measure scores from baseline were greater in early responders from W8 to W52.

CONCLUSIONEarly response to ivarmacitinib at W4 yields better long-term efficacy in patients with moderate-to-severe AD.

Abstract from PubMed

PMID 42454646 · DOI 10.1080/09546634.2026.2637340

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