Icotrokinra, a Targeted Oral Peptide, in Participants With Moderate-to-Severe Plaque Psoriasis and Self-Reported Psoriatic Arthritis: Results From a Pooled Analysis of the Phase 3 ICONIC-LEAD, ICONIC-ADVANCE 1, and ICONIC-ADVANCE 2 Trials.
10 affiliations
- 1MVLS College Office, Wolfson Medical School Building, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
- 2Henry Ford Health System, West Bloomfield, MI, USA.
- 3Innovaderm Research, Montreal, QC, Canada.
- 4Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
- 5Johnson & Johnson, Spring House, PA, USA.
- 6Johnson & Johnson, Horsham, PA, USA.
- 7Drexel University College of Medicine, Philadelphia, PA, USA.
- 8Johnson & Johnson, San Francisco, CA, USA.
- 9Department of Dermatology, University of California Los Angeles, Los Angeles, CA, USA.
- 10Department of Dermatology, and Department of Medicine, Division of Rheumatology, UT Southwestern Medical Center and O'Donnell School of Public Health, Dallas, TX, USA.
Abstract
Background
Icotrokinra, a targeted oral peptide that precisely blocks the interleukin-23 receptor, is approved to treat adult and pediatric (≥12 years, ≥40 kg) patients with moderate-to-severe plaque psoriasis (PsO).Objective
Assess psoriatic arthritis (PsA)-specific outcomes through Week (W) 16 in a subgroup of phase-3 study participants with moderate-to-severe plaque PsO and self-reported medical history of PsA (PsO+PsA).Methods
Post-hoc analyses pooled data from ICONIC-LEAD and ICONIC-ADVANCE 1 and 2 among PsO+PsA participants randomized to once-daily icotrokinra 200 mg or placebo through W16. PsA-specific outcomes included mean change from baseline and ≥50% improvement in Patient's Global Assessment (PtGA) of PsA disease activity and Patient's Assessment of PsA Pain, and percent change from baseline in modified Nail Psoriasis Severity Index (mNAPSI). P values are nominal.Results
Analyses included 216 participants (149 icotrokinra, 67 placebo). At W8, icotrokinra-treated participants reported greater improvements vs placebo in PtGA of PsA disease activity (-18.5 vs -4.8; P < 0.001) and PsA Pain (-17.1 vs -4.6; P < 0.001), with improvement sustained at W16 (-19.2 vs -0.8; P < 0.001; -19.5 vs -7.8; P = 0.003). At W16, greater proportions of icotrokinra-treated vs placebo-treated participants achieved ≥50% improvement in PtGA of PsA disease activity (47.0% vs 10.7%; P < 0.001) and PsA Pain (45.5% vs 16.1%; P < 0.001). At W16, icotrokinra improved mNAPSI by 41.6% (vs 118.6% worsening with placebo; P < 0.001). Adverse event rates were similar between icotrokinra and placebo.Conclusions
Icotrokinra demonstrated early, substantial improvements in participant-reported PsA activity and PsA Pain, and nail psoriasis, with a favorable safety profile through W16 in participants with PsO+PsA.
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BibTeX
@article{mcinnes2026icotrokinra,
title = {{Icotrokinra, a Targeted Oral Peptide, in Participants With Moderate-to-Severe Plaque Psoriasis and Self-Reported Psoriatic Arthritis: Results From a Pooled Analysis of the Phase 3 ICONIC-LEAD, ICONIC-ADVANCE 1, and ICONIC-ADVANCE 2 Trials.}},
author = {Iain B McInnes and Linda Stein Gold and Robert Bissonnette and Mark G Lebwohl and Ofelia Reyes-Servin and Joseph Cafone and Ya-Wen Yang and Soumya D Chakravarty and Charles Iaconangelo and Shu Li and Tasneam Shagroni and Karissa Lozenski and April W Armstrong and Joseph F Merola},
journal = {Journal of psoriasis and psoriatic arthritis},
year = {2026},
month = oct,
doi = {10.1177/24755303261494526},
url = {https://europepmc.org/article/MED/42898453},
note = {CC BY},
}
RIS
TY - JOUR
TI - Icotrokinra, a Targeted Oral Peptide, in Participants With Moderate-to-Severe Plaque Psoriasis and Self-Reported Psoriatic Arthritis: Results From a Pooled Analysis of the Phase 3 ICONIC-LEAD, ICONIC-ADVANCE 1, and ICONIC-ADVANCE 2 Trials.
AU - Iain B McInnes
AU - Linda Stein Gold
AU - Robert Bissonnette
AU - Mark G Lebwohl
AU - Ofelia Reyes-Servin
AU - Joseph Cafone
AU - Ya-Wen Yang
AU - Soumya D Chakravarty
AU - Charles Iaconangelo
AU - Shu Li
AU - Tasneam Shagroni
AU - Karissa Lozenski
AU - April W Armstrong
AU - Joseph F Merola
PY - 2026
DA - 2026/10/18
JO - Journal of psoriasis and psoriatic arthritis
DO - 10.1177/24755303261494526
UR - https://europepmc.org/article/MED/42898453
AB - Background Icotrokinra, a targeted oral peptide that precisely blocks the interleukin-23 receptor, is approved to treat adult and pediatric (≥12 years, ≥40 kg) patients with moderate-to-severe plaque psoriasis (PsO).Objective Assess psoriatic arthritis (PsA)-specific outcomes through Week (W) 16 in a subgroup of phase-3 study participants with moderate-to-severe plaque PsO and self-reported medical history of PsA (PsO+PsA).Methods Post-hoc analyses pooled data from ICONIC-LEAD and ICONIC-ADVANCE 1 and 2 among PsO+PsA participants randomized to once-daily icotrokinra 200 mg or placebo through W16. PsA-specific outcomes included mean change from baseline and ≥50% improvement in Patient's Global Assessment (PtGA) of PsA disease activity and Patient's Assessment of PsA Pain, and percent change from baseline in modified Nail Psoriasis Severity Index (mNAPSI). P values are nominal.Results Analyses included 216 participants (149 icotrokinra, 67 placebo). At W8, icotrokinra-treated participants reported greater improvements vs placebo in PtGA of PsA disease activity (-18.5 vs -4.8; P < 0.001) and PsA Pain (-17.1 vs -4.6; P < 0.001), with improvement sustained at W16 (-19.2 vs -0.8; P < 0.001; -19.5 vs -7.8; P = 0.003). At W16, greater proportions of icotrokinra-treated vs placebo-treated participants achieved ≥50% improvement in PtGA of PsA disease activity (47.0% vs 10.7%; P < 0.001) and PsA Pain (45.5% vs 16.1%; P < 0.001). At W16, icotrokinra improved mNAPSI by 41.6% (vs 118.6% worsening with placebo; P < 0.001). Adverse event rates were similar between icotrokinra and placebo.Conclusions Icotrokinra demonstrated early, substantial improvements in participant-reported PsA activity and PsA Pain, and nail psoriasis, with a favorable safety profile through W16 in participants with PsO+PsA.
SN - 2475-5303
SN - 2475-5311
ER -