Long-term benefits of upadacitinib for Atopic Dermatitis: deep responses in patient-reported outcomes over 140 weeks from the Measure Up 1 and Measure Up 2 clinical trials

OBJECTIVES: Atopic dermatitis (AD), a chronic, immune-mediated inflammatory disease, is characterized by intense itch, eczematous rash, and skin pain, which can have negative impacts to quality-of-life (QoL), sleep, and mental health (especially anxiety and depression). Evaluation of the impacts of AD on the patient's lived experience are most accurately assessed by the patient, making measures of patient-reported outcomes (PROs) indispensable. The objective of the current study was to assess the long-term impact of upadacitinib, a once-daily oral selective Janus kinase inhibitor approved for the treatment of moderate-to-severe AD, on patient-reported outcomes, providing a comprehensive in-depth evaluation of results of patient experience across multiple domains. METHODS: Using integrated data from the Measure Up 1 & 2 trials, the current study characterizes the efficacy of upadacitinib on several measures that assess the impact of AD on patients' lives, including patient-reported disease and symptom severity, sleep, emotional well-being, daily activities, QoL, and treatment satisfaction. RESULTS: Results demonstrated that rapid improvements in PRO measures of itch, sleep, daily activities, QoL, and emotional well-being reported at week 16 and week 52 were sustained or further improved at week 140 for patients with moderate-to-severe AD continuing upadacitinib 15 mg or 30 mg therapy, with no new safety signals observed. CONCLUSIONS: These findings support upadacitinib as a long-term treatment option to improve patient-reported burdensome symptoms of AD across 140 weeks of exposure.

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Publication Details

Journal
Journal of Dermatological Treatment
Published
2026-05-11
DOI
https://doi.org/10.1080/09546634.2026.2665961
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Long-term benefits of upadacitinib for Atopic Dermatitis: deep responses in patient-reported outcomes over 140 weeks from the Measure Up 1 and Measure Up 2 clinical trials

Ignasi Figueras‐Nart, Y. Armendáriz, Brian Calimlim, L. Stein Gold et al.
Journal of Dermatological Treatment
Dermatology and Skin Diseases
article

Long-term benefits of upadacitinib for Atopic Dermatitis: deep responses in patient-reported outcomes over 140 weeks from the Measure Up 1 and Measure Up 2 clinical trials

Ignasi Figueras‐Nart, Y. Armendáriz, Brian Calimlim, L. Stein Gold, Christopher G. Bunick, Alena Pechonkina, Xiaofei Hu, Ayman Grada, Raj Chovatiya, Vimal H. Prajapati, Bang Truong, Eric L. Simpson, Chao Li, Norito Katoh
article en

Abstract

OBJECTIVES: Atopic dermatitis (AD), a chronic, immune-mediated inflammatory disease, is characterized by intense itch, eczematous rash, and skin pain, which can have negative impacts to quality-of-life (QoL), sleep, and mental health (especially anxiety and depression). Evaluation of the impacts of AD on the patient's lived experience are most accurately assessed by the patient, making measures of patient-reported outcomes (PROs) indispensable. The objective of the current study was to assess the long-term impact of upadacitinib, a once-daily oral selective Janus kinase inhibitor approved for the treatment of moderate-to-severe AD, on patient-reported outcomes, providing a comprehensive in-depth evaluation of results of patient experience across multiple domains. METHODS: Using integrated data from the Measure Up 1 & 2 trials, the current study characterizes the efficacy of upadacitinib on several measures that assess the impact of AD on patients' lives, including patient-reported disease and symptom severity, sleep, emotional well-being, daily activities, QoL, and treatment satisfaction. RESULTS: Results demonstrated that rapid improvements in PRO measures of itch, sleep, daily activities, QoL, and emotional well-being reported at week 16 and week 52 were sustained or further improved at week 140 for patients with moderate-to-severe AD continuing upadacitinib 15 mg or 30 mg therapy, with no new safety signals observed. CONCLUSIONS: These findings support upadacitinib as a long-term treatment option to improve patient-reported burdensome symptoms of AD across 140 weeks of exposure.

Journal of Dermatological TreatmentVol. 37(1)
Henry Ford Health System (US), Oregon Health & Science University (US), University of Calgary (CA), Kyoto Prefectural University (JP), Rosalind Franklin University of Medicine and Science (US), Bellvitge University Hospital (ES), AbbVie (United States) (US), Kyoto Prefectural University of Medicine (JP), SKiN Health (CA), Probity Medical Research (CA), Institute of Immunology (HR), Dermatology Research Center (US)
AbbVie Canada
Good health and well-being
Openalex Percentile: Top 5%
Dermatology and Skin Diseases
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