Oral Icotrokinra for Plaque Psoriasis in Adults and Adolescents

Selective blockade of the interleukin-23 receptor with the targeted oral peptide icotrokinra resulted in a significantly higher incidence of skin clearance at week 16 than placebo among adults and adolescents with moderate-to-severe plaque psoriasis. Longer-term data will provide a more complete understanding of the benefit-risk profile of icotrokinra. (Funded by Johnson & Johnson; ICONIC-LEAD ClinicalTrials.gov number, NCT06095115.)See also in <i>NEJM Evidence</i>: Targeted Oral Peptide Icotrokinra for Psoriasis Involving High‑Impact Sites.

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Publication Details

Journal
New England Journal of Medicine
Published
2025-11-05
DOI
https://doi.org/10.1056/nejmoa2504187
Citations
9
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
Field-Weighted Citation Impact
7.18
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article

Oral Icotrokinra for Plaque Psoriasis in Adults and Adolescents

Jingzhi Jiang, Jennifer Soung, Andreas Pinter, Andrew Pink et al.
9 citations
New England Journal of Medicine
Psoriasis: Treatment and Pathogenesis
7.18
article

Oral Icotrokinra for Plaque Psoriasis in Adults and Adolescents

Jingzhi Jiang, Jennifer Soung, Andreas Pinter, Andrew Pink, Robert Bissonnette, Mark Lebwohl, Fabio P. Nunes, Adelaide A. Hebert, Cynthia Marie Carver DeKlotz, Angela Moore, Wenhui Wang, Shu Li, Yuling Shi, Joseph Cafone, Darryl Toth, Megan Miller-Kassamali
article en
9 citations

Abstract

Selective blockade of the interleukin-23 receptor with the targeted oral peptide icotrokinra resulted in a significantly higher incidence of skin clearance at week 16 than placebo among adults and adolescents with moderate-to-severe plaque psoriasis. Longer-term data will provide a more complete understanding of the benefit-risk profile of icotrokinra. (Funded by Johnson & Johnson; ICONIC-LEAD ClinicalTrials.gov number, NCT06095115.)See also in <i>NEJM Evidence</i>: Targeted Oral Peptide Icotrokinra for Psoriasis Involving High‑Impact Sites.

New England Journal of MedicineVol. 393(18)
Goethe University Frankfurt (DE), Tongji University (CN), University of North Texas (US), Texas Christian University (US), Johnson & Johnson (United States) (US), University of North Texas Health Science Center (US), Guy's and St Thomas' NHS Foundation Trust (GB), Peking University (CN), UCLA Medical Center (US), Baylor University Medical Center (US), Probity Medical Research (CA), University Hospital Frankfurt (DE), Johnson & Johnson (Israel) (IL), Innovaderm (Canada) (CA), Peking University Third Hospital (CN), Shanghai Skin Disease Hospital (CN), XLV Diagnostics (Canada) (CA), Arlington Center for Dermatology (US), Beijing Haidian Hospital (CN), Harbor–UCLA Medical Center (US), The University of Texas Medical Branch at Galveston (US), The University of Texas Health Science Center at Houston (US), Icahn School of Medicine at Mount Sinai (US)
Openalex Percentile: Top 2%
Psoriasis: Treatment and Pathogenesis
7.18
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