CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 277 enrolled
Drug / intervention
lirentelimab (AK002) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04322708
NCT04322708Phase 3Completed

A Phase 2/3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Lirentelimab (AK002) in Adult and Adolescent Patients With Active Eosinophilic Esophagitis

Allakos Inc.·interventional·Posted Mar 26, 2020·Updated Jan 2, 2024

In Brief

A Phase 3 clinical trial evaluating Placebo and lirentelimab (AK002) for Eosinophilic Esophagitis. Completed, enrolled 277 participants across 78 sites in 3 countries.

Detailed Summary

This is a Phase 2/3, multi-center, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of lirentelimab (AK002) given monthly for 6 doses in adult and adolescent patients with active eosinophilic esophagitis. Subjects who complete the randomized, double-blind, placebo-controlled treatment may have the option to receive 6 doses of open-label lirentelimab (AK002) through the OLE Period of the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Netherlands, United States
Collaborators--

Timeline

Phase 3CompletedFinished
202120222023202420252026
First PostedMar 26, 2020
Enrollment StartJul 6, 2020
Primary CompletionJun 4, 2021
Study CompletionJan 18, 2022
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 6.3 years ago

Interventions

Placeboother

Placebo

lirentelimab (AK002)drug

Lirentelimab (AK002) is a humanized non-fucosylated immunoglobulin G1 (IgG1) monoclonal antibody directed against Siglec-8.