Monoclonal antibodies for moderate-to-severe atopic dermatitis: a look at phase III and beyond

被引:3
作者
David, Eden [1 ]
Hawkins, Kelly [1 ,2 ]
Shokrian, Neda [1 ,2 ]
Del Duca, Ester [1 ,3 ]
Guttman-Yassky, Emma [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Dermatol, 5 East 98th St, New York, NY 10029 USA
[2] Albert Einstein Coll Med, Dept Dermatol, New York, NY USA
[3] Sapienza Univ Rome, Dept Clin Internal Anesthesiol & Cardiovasc Sci, Dermatol Clin, Rome, Italy
关键词
Atopic dermatitis; biologics; clinical trials; monoclonal antibodies; Phase; 3; Th2; ACTIVATION-REGULATED CHEMOKINE; 2-PHASE; 3; TRIALS; QUALITY-OF-LIFE; M RECEPTOR-BETA; DOUBLE-BLIND; DENDRITIC CELLS; ADULT PATIENTS; INTERLEUKIN-31; RECEPTOR; TOPICAL CORTICOSTEROIDS; ADOLESCENT PATIENTS;
D O I
10.1080/14712598.2024.2368192
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
IntroductionThe understanding of atopic dermatitis (AD) pathogenesis has rapidly expanded in recent years, catalyzing the development of new targeted monoclonal antibody treatments for AD.Areas coveredThis review aims to summarize the latest clinical and molecular data about monoclonal antibodies that are in later stages of development for AD, either in Phase 3 trials or in the pharmacopoeia for up to 5 years, highlighting the biologic underpinning of each drug's mechanism of action and the potential modulation of the AD immune profile.Expert opinionThe therapeutic pipeline of AD treatments is speedily progressing, introducing the potential for a personalized medical approach in the near future. Understanding how targeting pathogenic players in AD modifies disease progression and symptomatology is key in improving therapeutic choices for patients and identifying ideal patient candidates.
引用
收藏
页码:471 / 489
页数:19
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