Abstract |
Psoriasis is a chronic inflammatory skin disorder that affects 2% of the population. Evidence suggests that interleukin (IL)-23 plays a pivotal role in the pathogenesis of psoriasis. Guselkumab is a subcutaneously administered, humanized anti-IL23 monoclonal antibody indicated for the treatment of moderate-to-severe plaque psoriasis. Data from Phase I-III trials in this patient population reveal that guselkumab has proven to be superior to placebo or adalimumab based on achieving a Psoriasis Area and Severity Index (PASI) 90% reduction, or a static Physician Global Assessment (sPGA) score of 0 or 1 from baseline. This article reviews the current status of guselkumab as a therapy for moderate-to-severe plaque psoriasis.
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Authors | Z Nawas, M Hatch, E Ramos, M Liu, Y Tong, A Peranteau, S Tyring |
Journal | Skin therapy letter
(Skin Therapy Lett)
Vol. 22
Issue 2
Pg. 8-10
(Mar 2017)
ISSN: 1201-5989 [Print] Canada |
PMID | 28329405
(Publication Type: Journal Article, Review)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- Interleukin-23
- guselkumab
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Topics |
- Antibodies, Monoclonal
(administration & dosage, therapeutic use)
- Antibodies, Monoclonal, Humanized
- Clinical Trials as Topic
- Humans
- Interleukin-23
(antagonists & inhibitors)
- Psoriasis
(drug therapy, pathology)
- Severity of Illness Index
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