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. 2021 Oct 13;12:724277. doi: 10.3389/fimmu.2021.724277

Table 2.

Pharmacological therapies in development for the treatment of Atopic Dermatitis.

Drug candidate Target Possible mechanism of action on Atopic Dermatitis Disease indication Level of evidence NCT Number/PubMed ID
Baricitinib JAK1/JAK2 Inhibitor of JAK1 dan JAK2 mediated signaling in the immunopathology of AD (37) Rheumatoid arthritis Phase III completed NCT03334422, NCT03334396,
Tofacitinib JAK1/JAK2 Inhibitor of JAK1 and JAK2 inhibits cytokine IL-4 directly (38). Rheumatoid arthritis Phase II completed NCT02001181
Tralokinumab 1L13 Inhibitor of IL-13 by maintaining inflammatory reaction and major skin effects (39). Asthma Phase III completed NCT03160885
Ruxolitinib JAK1/JAK2 a selective inhibitor of JAK1 and JAK2 potently inhibits proinflammatory cytokine signaling (40) Myelofibrosis Phase III ongoing NCT03745651, NCT03745638
Upadacitinib JAK1 a selective inhibitor of JAK1 inhibited the production of proinflammatory Th2 cytokines such as IL-4 (41). Rheumatoid arthritis Phase III ongoing NCT04195698
Lebrikizumab IL13 Inhibitor of IL-13 by maintaining inflammatory reaction and major skin effects (39). Asthma Phase III ongoing NCT04392154
Pitrakinra IL13/IL4 IL-4/IL-13 inhibitory activity may reduce inflammation caused by allergens (39). Asthma Phase II completed NCT00676884
Tocilizumab# IL6R inhibits IL-6 binding to soluble IL6R (42). Rheumatoid arthritis Case series 21962991
Canakinumab* IL1B IL-1β induced TSLP production and stimulated keratinocytes (43). Familial Cold Autoinflammatory Syndrome (FCAS) 30937919
Momelotinib* JAK1/JAK2 JAK1 and JAK2 inhibitor could reduce inflammatory cytokine expression, including IL4, IL5, IFN-γ, and TSLP (44). Myelofibrosis 30544712

*Represents under preclinical investigation, #case series.