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. 2018 Jan 16;10(2):183–203. doi: 10.1080/19420862.2018.1415671

Table 1.

Antibody therapeutics approved in the European Union or United States during 2017*.

International non-proprietary name Brand name Target; Format Indication first approved Date of first EU approval Date of first US approval
Brodalumab Siliq, Lumicef, Kyntheum IL-17RA; Human IgG2 Plaque psoriasis 7/17/17 2/15/17
Avelumab Bavencio PD-L1; Human IgG1 Merkel cell carcinoma 9/18/17 3/23/17
Dupilumab Dupixent IL-4Rα; Human IgG4 Atopic dermatitis 9/27/17 3/28/17
Ocrelizumab Ocrevus CD20; Humanized IgG1 Multiple sclerosis EC decision pending 3/29/17
Durvalumab Imfinzi PD-L1; Human IgG1 Bladder cancer In review 5/1/17
Sarilumab Kevzara IL-6R; Human IgG1 Rheumatoid arthritis 6/23/17 5/22/17
Guselkumab Tremfya IL-23 p19; Human IgG1 Plaque psoriasis 11/23/17 7/13/17
Inotuzumab ozogamicin Besponsa CD22; Humanized IgG4; ADC Acute lymphoblastic leukemia 6/29/17 8/17/17
Benralizumab Fasenra IL-5R α; Humanized IgG1 Asthma EC decision pending 11/14/17
Emicizumab Hemlibra Factor IXa, X; Humanized IgG4, bispecific Hemophilia A In review 11/16/17

Table notes: Sarilumab's first global approval was granted in Canada on January 12, 2017; brodalumab's first global approval was granted in Japan on July 4, 2016. *Data available as of December 1, 2017

Abbreviations: ADC, antibody drug conjugate; CD, cluster of differentiation; EC, European Commission; EU, European Union; IL, interleukin; IgG, immunoglobulin G; PD-L1, programmed cell death 1.