Efficacy and safety of crisaborole ointment in Chinese and Japanese patients aged=2 years with mild-to-moderate atopic dermatitis

被引:7
|
作者
Ma, Lin [1 ]
Zhang, Litao [2 ]
Kobayashi, Michiko [3 ]
Tao, Xiaohua [4 ]
Qian, Qiufang [5 ]
Cheng, Hao [6 ]
Liu, Sujun [7 ]
Zhou, Yangmei [8 ]
Chen, Yayuan [8 ]
Zhang, Jianzhong [9 ,10 ]
机构
[1] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Beijing, Peoples R China
[2] Tianjin Acad, Tradit Chinese Med Affiliated Hosp, Tianjin, Peoples R China
[3] Sugamo Kobayashi Derma Clin, Tokyo, Japan
[4] Zhejiang Prov Peoples Hosp, Hangzhou, Zhejiang, Peoples R China
[5] Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Sch Med, Shanghai, Peoples R China
[6] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Hangzhou, Zhejiang, Peoples R China
[7] Hangzhou Third Peoples Hosp, Hangzhou, Zhejiang, Peoples R China
[8] Pfizer R&D China, Clin Dev, Shanghai, Peoples R China
[9] Peking Univ Peoples Hosp, Beijing, Peoples R China
[10] Peking Univ Peoples Hosp, Dept Dermatol, Beijing 100044, Peoples R China
关键词
Asian population; atopic dermatitis; crisaborole; efficacy; safety; SKIN-STRUCTURE; PETROLATUM; RESPONSES; CHILDREN; BURDEN; ECZEMA;
D O I
10.1111/1346-8138.16792
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis is a chronic inflammatory skin disease with a significant impact on the overall wellbeing of patients and their families. Crisaborole ointment, 2%, is a nonsteroidal phosphodiesterase 4 inhibitor approved for the treatment of mild-to-moderate atopic dermatitis in multiple countries. However, in the key pivotal trials, a low proportion of the overall patient population was Asian, therefore the safety and efficacy of crisaborole in the Asian population with atopic dermatitis remains unclear. CrisADe CLEAR was a multicenter, randomized, double-blind, vehicle-controlled, phase 3 study (NCT04360187) to assess the efficacy and safety of crisaborole ointment in Chinese and Japanese patients aged >= 2 years with mild-to-moderate atopic dermatitis involving >= 5% treatable body surface area. Patients were randomly assigned 2:1 to receive crisaborole or vehicle twice daily for 28 days. The primary endpoint was percentage change from baseline in the Eczema Area and Severity Index total score at day 29. Additional endpoints were improvement and success per Investigator's Static Global Assessment score at day 29 and change from baseline on the Peak Pruritus Numerical Rating Scale at week 4. Safety was assessed using rates of treatment emergent adverse events, serious adverse events, and clinically significant changes in vital signs and clinical laboratory parameters. Crisaborole-treated patients showed a significantly greater reduction versus vehicle in percentage change from baseline in Eczema Area and Severity Index total score at day 29 (P = 0.0002). Response rates for achievement of Investigator's Static Global Assessment improvement and success at day 29 were significantly higher for patients treated with crisaborole versus vehicle (P = 0.0124 and P = 0.0078, respectively). Crisaborole-treated patients showed a significantly greater reduction versus vehicle in change from baseline on the Peak Pruritus Numerical Rating Scale at week 4 (P = 0.0009). No new safety signals were identified. Treatment with crisaborole was effective and well tolerated in Chinese and Japanese patients with mild-to-moderate atopic dermatitis.
引用
收藏
页码:847 / 855
页数:9
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