Effect of secukinumab on clinical activity and disease burden of nail psoriasis: 32-week results from the randomized placebo-controlled TRANSFIGURE trial
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F19%3A43917263" target="_blank" >RIV/00216208:11120/19:43917263 - isvavai.cz</a>
Result on the web
<a href="https://doi.org/10.1111/bjd.17351" target="_blank" >https://doi.org/10.1111/bjd.17351</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/bjd.17351" target="_blank" >10.1111/bjd.17351</a>
Alternative languages
Result language
angličtina
Original language name
Effect of secukinumab on clinical activity and disease burden of nail psoriasis: 32-week results from the randomized placebo-controlled TRANSFIGURE trial
Original language description
BACKGROUND: Nail psoriasis is associated with functional impairment, pain and reduced quality of life. OBJECTIVE: To demonstrate the superiority of secukinumab vs. placebo in clearing nail psoriasis as assessed by NAil Psoriasis Severity Index (NAPSI) at Week 16 and over time up to Week 132. Presented here is the Week 32 interim analysis. Impact on quality of life was assessed by Nail Assessment in Psoriasis and Psoriatic Arthritis (NAPPA) patient questionnaires. METHODS: TRANSFIGURE is a double-blind, randomized, placebo-controlled study in subjects with moderate to severe plaque and nail psoriasis. RESULTS: The primary objective of this study was met: both doses of secukinumab were superior to placebo at Week 16 (NAPSI improvement of -45.3%, -37.9%, and -10.8%, for secukinumab 300 mg, 150 mg and placebo, respectively, P<0.0001). Significant improvements were seen in patients' quality of life: NAPPA-QOL total score median decrease at Week 16 was 60.9%, 49.9% and 15.8% for secukinumab 300 mg, 150 mg and placebo, respectively (P<0.0001). Improvement in nail psoriasis continued to Week 32: NAPSI % change reached -63.2% and -52.6%, for secukinumab 300 mg and 150 mg, respectively. Skin clearance was significant (PASI 90: 72.5%, 54.0% and 1.7% for secukinumab 300 mg, 150 mg and placebo at Week 16, respectively, P<0.0001) and was sustained to Week 32. The most common adverse events were nasopharyngitis, headache, and upper respiratory tract infections. CONCLUSIONS: Secukinumab demonstrated significant and clinically meaningful efficacy and quality of life improvements for patients with nail psoriasis up to Week 32.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30216 - Dermatology and venereal diseases
Result continuities
Project
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Continuities
N - Vyzkumna aktivita podporovana z neverejnych zdroju
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
British Journal of Dermatology
ISSN
0007-0963
e-ISSN
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Volume of the periodical
181
Issue of the periodical within the volume
5
Country of publishing house
GB - UNITED KINGDOM
Number of pages
13
Pages from-to
954-966
UT code for WoS article
000493737200016
EID of the result in the Scopus database
2-s2.0-85060149116