ANCA-associated vasculitis is a rare, life-threatening autoimmune disease with a relapsing nature. ANCA-Associated vasculitis comprises three autoimmune disorders, i.e. Granulomatosis with Polyangiitis (GPA), Microscopic Polyangiitis (MPA), and Eosinophilic Granulomatosis with Polyangiitis (EGPA). The global yearly incidence of ANCA-associated vasculitis ranges from 1.2 to 3.3 cases per 100,000 people, with a prevalence of 4.6-42.1 instances per 100,000 people.
As per DelveInsight’s estimates, as of 2022, ~210K people were diagnosed with ANCA-associated vasculitis across the 7MM. In the 7MM, the United States, EU4, the UK, and Japan accounted for aroun...
