remibrutinib (LOU064) - Novartis
ligelizumab (QGE 031) - Novartis
Xolair (omalizumab) - Roche, Novartis
Tezspire (tezepelumab) - AstraZeneca, Amgen
Nucala (mepolizumab) - GSK
fenebrutinib (GDC-0853) - Roche
UB-221 - United BioPharma
CDX-0159 - Celldex
Fasenra (benralizumab) - AstraZeneca
Dupixent (dupilumab) - Sanofi, Regeneron
rilzabrutinib (SAR444671) - Sanofi
Emerging treatments for chronic urticaria. (PubMed, Expert Opin Investig Drugs) - Mar 29, 2022 - "While three omalizumab biosimilars are investigated, the assumed early approval of ligelizumab will expand the effective and safe anti-IgE approach observed with omalizumab. For other anti-IgEs like UB-221, the development is behind. Data are too limited so far to clearly define the role of anti-cytokine and anti-cytokine receptor biologics such as dupilumab, tezepelumab, mepolizumab, benralizumab, and CDX-0159, of which only dupilumab is actually investigated in phase 3. Among three selective oral BTK inhibitors, remibrutinib, rilzabrutinib, and fenebrutinib, the development of remibrutinib is most advanced (phase 3). As the pipeline addresses different targets, study results will give deeper insights into the pathomechanisms of CU. Hopefully, in the next future additional approved and also more targeted approaches will be available." 
Clinical • Journal • Review • Chronic Spontaneous Urticaria • Dermatology • Urticaria
http://www.ncbi.nlm.nih.gov/pubmed/35166638
 
Mar 29, 2022
 
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