This post-hoc analysis examined T2T outcomes in patients from UNCOVER-3 receiving the label dose of ixekizumab receiving the label dose of ixekizumab, finding early and maintained response was defined as achievement of T2T goals at Week12 maintained at 5 years (Week264).
Abstract
Background. The National Psoriasis Foundation recommends evaluating treatment response at Week12, with a target body surface area (BSA) ≤1% affected and an acceptable response of BSA≤3%1. European consensuses emphasize a shift from relative outcomes such as Psoriasis Area and Severity Index (PASI) scores of 90/100 towards absolute endpoints including PASI≤22. Early achievement and long-term maintenance of these treat-to-target (T2T) outcomes are important, providing patients with more days of minimal disease burden.Methods. UNCOVER-3 (NCT01646177) was a multicenter, randomized, double-blind, placebo-controlled study of ixekizumab in patients with moderate-to-severe psoriasis3. This post-hoc analysis examined T2T outcomes in patients from UNCOVER-3 receiving the label dose of ixekizumab (N=385). Baseline demographics and patient characteristics were similar to those previously presented4. Early and maintained response was defined as achievement of T2T goals at Week12 maintained at 5 years (Week264). Assessments included absolute PASI≤2, absolute PASI≤1, BSA≤3%, and BSA≤1%, reported as observed. No statistical testing for significance was conducted.Results. At Week12, absolute PASI
Xeligekimab provides rapid symptom resolution across all clinical dimensions, high and sustained achievement of treatment targets, and comprehensive restoration of quality of life in Chinese patients.
Kun Huang, Yi Zhao, Chun-Jun Yang et al.· Frontiers in Immunology· 0 citations
Introduction. Overweight and obesity affect 60%-78% of patients with psoriasis, impacting disease severity, treatment response (i.e., complete skin clearance), and clinical outcomes. This trial evaluated efficacy and safety of ixekizumab (IXE) with or without tirzepatide (TZP) in participants with psoriasis and overwei...
Associazione Dermatologi-Venereologi Ospedalieri Italiani e della Sanità Pubblica· Dermatology Reports· 0 citations
Abstract Objective This post hoc analysis of the SELECT-PsA 2 study evaluated long-term efficacy and safety of upadacitinib 15 mg once daily in patients with psoriatic arthritis (PsA) and exposure to one prior tumour necrosis factor inhibitor (TNFi). Methods Patients were randomised to upadacitinib 15 mg once daily or...
L. Coates, P. Mease, A. Kavanaugh et al.· RMD Open· 0 citations
Adalimumab, a monoclonal antibody targeting tumor necrosis factor-alpha, has been approved for the treatment of severe plaque psoriasis in children aged 4 years and older. Data on its use in the clinical management of pediatric psoriasis in China remains limited. This study is the first prospective analysis of the adal...
Yi-Rong Huang, Ting Pan, Xin Shi et al.· Dermatologic Therapy· 0 citations
BACKGROUND
Treatment options for paediatric patients with psoriasis are limited, and additional, more advanced therapies are needed. Risankizumab is an interleukin-23 inhibitor approved to treat moderate-to-severe psoriasis in adults.
OBJECTIVES
To evaluate efficacy and safety of risankizumab through 52 weeks in paed...
N. Magnolo, Wine Lee Lara, A. Reich et al.· British Journal of Dermatolo...· 0 citations
Introduction Brodalumab is the only interleukin-17 (IL-17) receptor A blocker approved for moderate-to-severe plaque psoriasis and blocks downstream signaling of multiple IL-17 isoforms including IL-17A, IL-17F, IL-17C, IL-17E, and IL-17A/F. Here, we contextualize effectiveness and safety of brodalumab in adult patient...
Marni Wiseman, Sunil Kalia, C. Lynde et al.· SKIN The Journal of Cutaneou...· 0 citations
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