A Review of Phase 3 Trials of Dupilumab for the Treatment of Atopic Dermatitis in Adults, Adolescents, and Children Aged 6 and Up

被引:7
|
作者
Cather, Jennifer [1 ]
Young, Melodie [1 ]
DiRuggiero, Douglas C. [2 ]
Tofte, Susan [3 ]
Williams, Linda [4 ]
Gonzalez, Tayler [5 ]
机构
[1] Mindful Dermatol & Modern Res Associates, Dallas, TX USA
[2] Skin Canc & Cosmet Dermatol Ctr, Rome, GA USA
[3] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[4] Regeneron Pharmaceut Inc, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
[5] Sanofi, Cambridge, MA 02139 USA
关键词
Atopic dermatitis; Dupilumab; Efficacy; Safety; Adults; Children; Adolescents; PERSISTENT ASTHMA; SYSTEMIC THERAPY; INCREASED RISK; MODERATE; PLACEBO; HUMANIZATION; INFECTIONS; MANAGEMENT; HEALTH; SAFETY;
D O I
10.1007/s13555-022-00778-y
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis (AD) is a chronic pruritic skin disease that can have a profound negative impact on patients' quality of life, especially in cases of inadequate disease control. Dupilumab, a dual inhibitor of IL-4 and IL-13 signaling, is approved in the United States for the treatment of moderate-to-severe AD in adults (>= 18 years old) and in children (>= 6 years old). In this review, we present results from phase 3 trials evaluating dupilumab's efficacy and safety in adults, adolescents, and children. These trials demonstrate that dupilumab provides rapid improvements (in as little as 1 week) and sustained efficacy (up to 4 years) when used as a treatment for moderate-to-severe AD. Dupilumab not only improves skin signs and symptoms, but also provides multiple health benefits beyond the skin, including improvements in quality of life, itch, sleep disturbances, and pain/discomfort. Dupilumab is generally well tolerated, has a favorable safety profile in adults, adolescents, and children, has no serious drug-drug interactions, does not require routine laboratory testing, and is not an immunosuppressant. Taken together, phase 3 trials demonstrate that dupilumab provides rapid and sustained efficacy and is generally well tolerated for the treatment of moderate-to-severe AD across age groups.
引用
收藏
页码:2013 / 2038
页数:26
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