By Ben Glickman

 

AstraZeneca said Monday that a Phase 3 trial of its treatment for eosinophilic granulomatosis with polyangiitis, a rare form of vasculitis, met its primary endpoint.

The pharmaceutical company said that its trial of Fasenra also demonstrated non-inferior rates of remission compared to mepolizumab, the only approved treatment for EGPA.

The company said that EGPA is a rare disease caused by inflammation of small to medium-sized blood vessels. About half of patients with EGPA develop a form of asthma, and the disease can cause damage to organs.

Fasenra received orphan drug designation from the U.S. Food and Drug Administration as a treatment for EGPA. The company said that the treatments safety and tolerability profile in the trial was consistent with Fasenra's profile, and that the full results of the trial would be presented at an upcoming medical meeting.

 

Write to Ben Glickman at ben.glickman@wsj.com

 

(END) Dow Jones Newswires

September 11, 2023 13:33 ET (17:33 GMT)

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