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Anti–Siglec-8 Antibody for Eosinophilic Gastritis and Duodenitis

Authors :
Michael F. Vaezi
Chao Wang
Joseph A. Murray
Sandy R. Durrani
Gary W. Falk
Marc E. Rothenberg
Sabine Hazan
Paneez Khoury
Mirna Chehade
Alan T. Chang
Evan S. Dellon
Henrik S. Rasmussen
Kathryn A. Peterson
Bhupinder Singh
Ikuo Hirano
Nirmala Gonsalves
Adam C. Bledsoe
Amy D. Klion
Robert M. Genta
Camilla Shaw
Amol P. Kamboj
John Leung
Source :
N Engl J Med
Publication Year :
2020

Abstract

BACKGROUND: Eosinophilic gastritis and duodenitis are characterized by gastrointestinal mucosal eosinophilia, chronic symptoms, impaired quality of life, and a lack of adequate treatments. Mast-cell activity may contribute to the pathogenesis of the conditions. AK002 (lirentelimab) is an anti–Siglec-8 antibody that depletes eosinophils and inhibits mast cells and that has shown potential in animal models as a treatment for eosinophilic gastritis and duodenitis. METHODS: In this phase 2 trial, we randomly assigned adults who had symptomatic eosinophilic gastritis, eosinophilic duodenitis, or both conditions in a 1:1:1 ratio to receive four monthly infusions of low-dose AK002, high-dose AK002, or placebo. The primary end point was the change in gastrointestinal eosinophil count from baseline to 2 weeks after the final dose; to maximize statistical power, we evaluated this end point in the placebo group as compared with the combined AK002 group. Secondary end points were treatment response (>30% reduction in total symptom score and >75% reduction in gastrointestinal eosinophil count) and the change in total symptom score. RESULTS: Of the 65 patients who underwent randomization, 43 were assigned to receive AK002 and 22 were assigned to receive placebo. The mean percentage change in gastrointestinal eosinophil count was −86% in the combined AK002 group, as compared with 9% in the placebo group (least-squares mean difference, −98 percentage points; 95% confidence interval [CI], −121 to −76; P

Details

Language :
English
Database :
OpenAIRE
Journal :
N Engl J Med
Accession number :
edsair.doi.dedup.....2d0ab6132157a4b47283279c9f4c4700