- Part A: 60% of patients with DUPIXENT (n=42) vs 5% with placebo (n=39) (P<0.001)
DUPIXENT demonstrated greater histologic improvements compared to placebo at Week 24.1,3
Histologic improvements were observed at Week 52 with continued weekly DUPIXENT treatment.1,3
Extended active treatment period, results are descriptive at Week 52. Definitive conclusions cannot be made due to limitations associated with extended active treatment design, including lack of comparator arm and decreasing sample size.3
aCoprimary endpoint at Week 24;
secondary endpoint at Week 52.1,3
bSecondary endpoint at Weeks 24 and 52.
In Part B, this endpoint was ordered after the point at which hierarchical testing procedure failed; results are
descriptive.3
To be eligible to participate in the study, all participants must have had uncontrolled EoE as defined by ≥15 intraepithelial EOS/HPF despite an 8-week course of a high-dose PPI and a Dysphagia Symptom Questionnaire (DSQ) score of ≥10.1,4
Histologic improvements were defined as the proportion of participants who achieved peak esophageal intraepithelial eosinophil counts of <15 EOS/HPF (histologic response) or ≤6 EOS/HPF (histologic remission).1