2018
DOI: 10.1111/bjd.16505
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After the approval of dupilumab for moderate-to-severe atopic dermatitis: what is next on the research agenda?

Abstract: Linked Article: de Bruin‐Weller et al. Br J Dermatol 2018; 178:1083–1101.

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“…Recently, multiple clinical trials have demonstrated the efficacy of targeted therapy involving the blocking of cytokines or mediators that play a pivotal role in the pathogenesis of AD. Dupilumab is currently the only biologic drug that has been approved by both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of adult patients with inadequately controlled moderate-to-severe AD [ 12 ]. Biological drugs appear to be promising treatments for adult AD patients because they offer more convenient dose regimens and allow less frequent laboratory monitoring than other systemic therapies, as well as having fewer side effects [ 1 ].…”
Section: Biologic Drugsmentioning
confidence: 99%
“…Recently, multiple clinical trials have demonstrated the efficacy of targeted therapy involving the blocking of cytokines or mediators that play a pivotal role in the pathogenesis of AD. Dupilumab is currently the only biologic drug that has been approved by both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of adult patients with inadequately controlled moderate-to-severe AD [ 12 ]. Biological drugs appear to be promising treatments for adult AD patients because they offer more convenient dose regimens and allow less frequent laboratory monitoring than other systemic therapies, as well as having fewer side effects [ 1 ].…”
Section: Biologic Drugsmentioning
confidence: 99%