MESSINA did not meet one of the two dual-primary endpoints, demonstrating a statistically significant improvement in histological disease remission with Fasenra, but not in dysphagia symptoms, compared to placebo

LONDON, UK I October 25, 2022 I Eosinophilic esophagitis (EoE) is a rare, progressive, chronic inflammatory disease of the esophagus currently believed to be characterised by the abnormal presence of eosinophils, a type of white blood cell, in the inner lining of the esophagus.1-3 Patients experience difficulty with swallowing (dysphagia), pain, food getting stuck and anxiety.4,5

High-level results from the MESSINA Phase III trial showed that AstraZeneca’s Fasenra (benralizumab) did not meet one of the two dual-primary endpoints. Fasenra demonstrated a statistically significant improvement in histological disease remission, but not a change in dysphagia symptoms, compared to placebo, in patients with EoE aged 12 years or older.

Mene Pangalos, Executive Vice President, BioPharmaceuticals R&D, AstraZeneca said: “The results from the MESSINA Phase III trial in eosinophilic esophagitis confirm that Fasenra achieved near complete depletion of tissue eosinophils, consistent with its mechanism of action, however this did not translate into an improvement in dysphagia symptoms. We will continue to analyse the complete data set to share with the scientific community.”

In the trial, histological disease remission was measured as the proportion of patients with less than or equal to six eosinophils per high power field at Week 24. Burden of dysphagia was assessed using the patient-reported Dysphagia Symptom Questionnaire (DSQ) and measured as a mean change from baseline at Week 24. The trial included 210 patients, who received either Fasenra or placebo at four-week intervals.

The safety and tolerability profile for Fasenra in the trial was consistent with the known profile of the medicine.

Results from MESSINA will be presented at an upcoming medical meeting.

Fasenra is currently approved as an add-on maintenance treatment for severe eosinophilic asthma in the US, EU, Japan and other countries,6 and is approved for self-administration in the US,6 EU7 and other countries.


MESSINA is a randomised, placebo-controlled, double-blind, parallel-group, multicentre, global Phase III trial designed to investigate the efficacy and safety of Fasenra compared to placebo in patients aged 12 to 65 years of age with symptomatic and histologically active EoE.8,9

The dual-primary endpoints analysed at Week 24 were the proportion of patients with a histologic response, defined as a peak esophageal eosinophil count less than or equal to 6 eosinophils per high power field, and mean changes from baseline in Dysphagia Symptom Questionnaire (DSQ).8 The peak eosinophil count is obtained when a biopsy of the tissue of the esophagus is examined under a microscope. The histologic response endpoint used in the trial is consistent with histologic remission.10 The DSQ captures the presence and severity of dysphagia symptoms in the past day in a 4-item patient-reported questionnaire and the score is calculated over 14-day periods, ranging from 0 to 84, with a lower score indicating less severe dysphagia.8

The trial period consists of a 24-week double-blind, placebo-controlled treatment period followed by a 28-week open-label treatment period.8 Eligible patients were randomised in a 1:1 ratio to receive either 30 mg of Fasenra or placebo at 4-week intervals for the double-blind period. Patients who complete the double-blind period on Fasenra continue into the open-label treatment period with all patients receiving Fasenra 30 mg at 4-week intervals until Week 52, with a further open-label extension offered to eligible patients thereafter.9

In the trial, patients were allowed to remain on background medications for EoE, including proton pump inhibitors, topical corticosteroids, and EoE-driven diet elimination, provided that they were stable prior to entry and during the first 52 weeks of treatment, unless changes were clinically indicated.8,9

Fasenra (benralizumab) is a monoclonal antibody that binds directly to IL-5 receptor alpha on eosinophils and attracts natural killer cells to induce rapid and near-complete depletion of blood and tissue eosinophils in most patients via apoptosis (programmed cell death).11

Fasenra is currently approved as an add-on maintenance treatment for severe eosinophilic asthma in the US, EU, Japan and other countries,6 and is approved for self-administration in the US,6 EU7 and other countries. Fasenra has been studied in almost 4,000 patients in global clinical trials.12-16

Fasenra is in development for other eosinophilic diseases including bullous pemphigoid, chronic obstructive pulmonary disease, chronic rhinosinusitis with nasal polyps, chronic spontaneous urticaria, eosinophilic esophagitis, eosinophilic gastritis/eosinophilic gastroenteritis, eosinophilic granulomatosis with polyangiitis, hypereosinophilic syndrome and non-cystic fibrosis bronchiectasis.

Fasenra was developed by AstraZeneca and is in-licensed from BioWa, Inc., a wholly-owned subsidiary of Kyowa Kirin Co., Ltd., Japan. 

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SOURCE: AstraZeneca