CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 36 enrolled
Drug / intervention
IRL201104 +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/NCT05084963
NCT05084963Phase 2Completed

A Phase 2a, Double-blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy, Safety, and Tolerability of IRL201104 in Adult Participants With Active Eosinophilic Esophagitis (EoE)

Revolo Biotherapeutics·interventional·Posted Oct 20, 2021·Updated May 21, 2025

In Brief

A Phase 2 clinical trial evaluating IRL201104 and Placebo for Eosinophilic Esophagitis. Completed, enrolled 36 participants across 23 sites.

Detailed Summary

The purpose of this study is to asses the efficacy, safety and tolerability of repeat doses of IRL201104 in Adult Participants with Active Eosinophilic Esophagitis (EoE)

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20222023202420252026
First PostedOct 20, 2021
Enrollment StartOct 29, 2021
Primary CompletionOct 24, 2022
TodayJul 2, 2026
Enrollment to primary: 12 monthsPosted 4.7 years ago

Interventions

IRL201104drug

lyophilised powder for reconstitution for IV dosing

Placebodrug

Matching placebo for IRL201104