Emerging pharmacotherapies for chronic spontaneous urticaria: spotlight on BTK inhibitors.

Abstract

Introduction: Chronic spontaneous urticaria (CSU) results from multiple interacting pathogenic mechanisms. Despite available treatments, a proportion of patients remain inadequately controlled, supporting the need for therapeutic options.

Areas covered: This review examines the role of Bruton's tyrosine kinase (BTK) in CSU and summarizes the development of BTK inhibitors. Data on fenebrutinib, remibrutinib, rilzabrutinib, TAS5315, and other emerging agents are reviewed, focusing on mechanisms of action, efficacy, safety, and their potential place in practice. TAS5315 remains at an earlier stage of development, with CSU findings available from conference abstracts and registry data. The literature search included PubMed-indexed articles, clinical trial reports, regulatory documents, and congress presentations relevant to BTK inhibition in CSU.

Expert opinion: BTK inhibitors act on intracellular pathways involved in mast-cell activation, basophil signaling, and B-cell mediated immune responses. Studies have shown reductions in disease activity across multiple BTK inhibitors, with benefit observed early after treatment initiation in several studies. Remibrutinib is the first BTK inhibitor approved for CSU and has the most extensive phase 3 evidence. Oral administration may provide a treatment option for patients. Defining the place of BTK inhibitors within treatment algorithms and identifying patients most likely to benefit from this approach remain areas for future research.