drugset / Trial / NCT05583227

Efficacy and Safety of Tezepelumab in Patients With Eosinophilic Esophagitis

NCT05583227

Phase 3 Active not recruiting 368 enrolled AstraZeneca Amgen · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomized, double-blind, placebo-controlled multicenter, phase 3 study to evaluate the efficacy and safety of tezepelumab administered subcutaneously (SC) using an accessorized pre-filled syringe (APFS) versus placebo in adult and adolescent patients with eosinophilic esophagitis (EoE).

Timeline

Start
2022-11-10
Primary completion
2026-07-14
Completion
2027-03-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Tezepelumab Monoclonal antibody Subcutaneous