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Completed Phase 3 Interventional Results available

An Extension Study of Lirentelimab in Eosinophilic Gastritis and/or Eosinophilic Duodenitis (Formerly Referred to as Eosinophilic Gastroenteritis)

ClinicalTrials.gov ID: NCT04620811

Public ClinicalTrials.gov record NCT04620811. 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 20, 2026, 10:57 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 Phase 3, Multicenter, Open-Label, Extension Study to Evaluate the Efficacy and Safety of AK002 in Patients That Were Previously Enrolled in AK002-016 or AK002-012 Studies and Have Eosinophilic Gastritis and/or Eosinophilic Duodenitis (Formerly Referred to as Eosinophilic Gastroenteritis)

Brief summary

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

This is a Phase 3, open-label, extension study to assess the long term efficacy and safety of lirentelimab given monthly.

Study identification

NCT ID
NCT04620811
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Allakos Inc.
Industry
Enrollment
159 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Dec 3, 2020 (Actual)
Primary completion
May 15, 2023 (Actual)
Completion
Jul 7, 2023 (Actual)
Last update posted
Apr 22, 2024

2020 – 2023

United States locations

U.S. sites
38
U.S. states
19
U.S. cities
33
Facility City State ZIP Site status
Allakos Investigational Site 216-068 Birmingham Alabama 35209 —
Allakos Investigational Site 216-002 Huntsville Alabama 35802 —
Allakos Investigational Site 216-035 Phoenix Arizona 85018 —
Allakos Investigational Site 216-032 Chula Vista California 91910 —
Allakos Investigational Site 216-014 Santa Monica California 90404 —
Allakos Investigational Site 216-038 Tustin California 92780 —
Allakos Investigational Site 216-049 Walnut Creek California 94598 —
Allakos Investigational Site 216-034 Aurora Colorado 80045 —
Allakos Investigational Site 216-063 Brandon Florida 33511 —
Allakos Investigational Site 216-027 Edgewater Florida 32132 —
Allakos Investigational Site 216-056 Jacksonville Florida 32256 —
Allakos Investigational Site 216-013 Miami Florida 33176 —
Allakos Investigational Site 216-053 New Port Richey Florida 34653 —
Allakos Investigational Site 216-007 Chicago Illinois 60611 —
Allakos Investigational Site 216-001 Crowley Louisiana 70526 —
Allakos Investigational Site 216-026 Boston Massachusetts 02111 —
Allakos Investigational Site 216-052 Boston Massachusetts 02115 —
Allakos Investigational Site 216-051 Boston Massachusetts 02215 —
Allakos Investigational Site 216-005 Rochester Minnesota 55905 —
Allakos Investigational Site 216-042 Kansas City Missouri 64108 —
Allakos Investigational Site 216-045 Reno Nevada 89511 —
Allakos Investigational Site 216-025 New York New York 10029 —
Allakos Investigational Site 216-020 Chapel Hill North Carolina 27599 —
Allakos Investigational Site 216-048 Durham North Carolina 27710 —
Allakos Investigational Site 216-050 Winston-Salem North Carolina 27157 —
Allakos Investigational Site 216-031 Cincinnati Ohio 45229 —
Allakos Investigational Site 216-028 Cincinnati Ohio 45236 —
Allakos Investigational Site 216-044 Mentor Ohio 44060 —
Allakos Investigational Site 216-021 Philadelphia Pennsylvania 19104 —
Allakos Investigational Site 216-006 Chattanooga Tennessee 37343 —
Allakos Investigational Site 216-003 Chattanooga Tennessee 37404 —
Allakos Investigational Site 216-011 Chattanooga Tennessee 37421 —
Allakos Investigational Site 216-062 Kingsport Tennessee 37663 —
Allakos Investigational Site 216-022 Austin Texas 78742 —
Allakos Investigational Site 216-039 Ogden Utah 84405 —
Allakos Investigational Site 216-030 Salt Lake City Utah 84132 —
Allakos Investigational Site 216-055 Sandy City Utah 84092 —
Allakos Investigational Site 216-064 Spokane Washington 99202 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04620811, 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 Apr 22, 2024 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04620811 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →