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Unmasking EGPA: Enhancing HCP Awareness, Early Detection, and Disease Management to Improve Patient Outcomes

Clinical Thought

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis, yet its prevalence is on the rise. Learn why early detection and multidisciplinary management of patients with EGPA is critical and what novel biologics are transforming the treatment landscape.

Released: August 28, 2025

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Provided by Clinical Care Options, LLC.

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Supported by an educational grant from AstraZeneca.

AstraZeneca

Disclosure

Primary Author

Anisha Dua, MD, MPH: consultant/advisor/speaker: AbbVie, Amgen, AstraZeneca, GlaxoSmithKline, Novartis, Sanofi; researcher: Amgen, Novartis.