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Active, not recruiting Phase 3 Interventional

Efficacy and Safety of Tezepelumab in Patients With Eosinophilic Esophagitis

ClinicalTrials.gov ID: NCT05583227

Public ClinicalTrials.gov record NCT05583227. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 2:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Phase 3 Efficacy and Safety Study of Tezepelumab in Patients With Eosinophilic Esophagitis (CROSSING).

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT05583227
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
368 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
12 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 10, 2022 (Actual)
Primary completion
Jul 14, 2026 (Actual)
Completion
Mar 23, 2027 (Estimated)
Last update posted
Jul 30, 2026

2022 – 2027

United States locations

U.S. sites
24
U.S. states
20
U.S. cities
23
Facility City State ZIP Site status
Research Site Phoenix Arizona 85016 —
Research Site Little Rock Arkansas 72202 —
Research Site Los Angeles California 90033 —
Research Site Aurora Colorado 80045 —
Research Site Inverness Florida 34452 —
Research Site Jacksonville Florida 32256 —
Research Site Saint Augustine Florida 32086 —
Research Site Normal Illinois 61761 —
Research Site Iowa City Iowa 52242 —
Research Site Topeka Kansas 66606 —
Research Site White Marsh Maryland 21162 —
Research Site Boston Massachusetts 02111 —
Research Site Chesterfield Michigan 48047 —
Research Site Lincoln Nebraska 68503 —
Research Site Ocean City New Jersey 07712 —
Research Site Brooklyn New York 11235 —
Research Site Chapel Hill North Carolina 27599 —
Research Site Cincinnati Ohio 45229 —
Research Site Philadelphia Pennsylvania 19104 —
Research Site Uniontown Pennsylvania 15401 —
Research Site Nashville Tennessee 37232 —
Research Site Houston Texas 77030 —
Research Site Salt Lake City Utah 84107 —
Research Site Salt Lake City Utah 84132 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 100 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05583227, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 30, 2026 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05583227 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →