Drug intelligence / Profile preview

TAS5315

Development stage
Phase 2
Lead developer
Taiho Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

TAS5315 is a highly potent and selective small molecule inhibitor of Bruton’s tyrosine kinase (BTK), developed by Taiho Pharmaceutical for the treatment of autoimmune and allergic diseases, including rheumatoid arthritis (RA) and chronic spontaneous urticaria (CSU). It acts as an irreversible covalent inhibitor of BTK, blocking B-cell receptor signaling pathways that are implicated in the pathogenesis of these conditions. Preclinical studies demonstrated anti-inflammatory effects in models of arthritis and lupus, with reductions in inflammatory cytokines such as TNF-alpha, IL-1β, and IL-6. Clinical trials have shown dose-dependent BTK occupancy, inhibition of basophil activation, improvements in RA disease activity measures, and efficacy signals in CSU patients refractory to antihistamines. The drug is administered orally

Other names
TAS5315TAS-5315TAS 5315
02

Targets

ERBB4 (Erb-b2 receptor tyrosine kinase 4)EGFR T790M (Epidermal growth factor receptor T790M mutant)JAK3 (Janus kinase 3)BTK (Bruton tyrosine kinase)

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