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Clinical trialNCT04157348Active, not recruitingPhase 3Interventional

Efficacy and Safety of Benralizumab in EGPA Compared to Mepolizumab.

SponsorAstraZenecaEnrollment140Eosinophilic Granulomatous Vasculitis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a randomized, double blind, active-controlled, parallel group, multicenter 52-week Phase 3 study to compare the efficacy and safety of benralizumab 30 mg versus mepolizumab 300 mg administered by subcutaneous (SC) injection in patients with relapsing or refractory EGPA on corticosteroid therapy with or without stable immunosuppressive therapy. All patients who complete the 52-week double-blind treatment period on IP may be eligible to continue into an open label extension (OLE) period. The OLE period is intended to allow each patient at least 1 year of treatment with open-label benralizumab 30 mg administered SC (earlier enrolled patients may therefore be in the OLE for longer than 1 year).

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

50 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Belgium
  • Research Site

    Brussels, Belgium

  • Research Site

    Brussels, Belgium

Canada
  • Research Site

    Calgary, Alberta, Canada

  • Research Site

    Hamilton, Ontario, Canada

  • Research Site

    Toronto, Ontario, Canada

  • Research Site

    Toronto, Ontario, Canada

France
  • Research Site

    Dijon, France

  • Research Site

    Marseille, France

  • Research Site

    Montpellier, France

  • Research Site

    Nantes, France

  • Research Site

    Paris, France

  • Research Site

    Paris, France

  • Research Site

    Suresnes, France

  • Research Site

    Toulouse, France

Germany
  • Research Site

    Bamberg, Germany

  • Research Site

    Freiburg im Breisgau, Germany

  • Research Site

    Hamburg, Germany

  • Research Site

    Kirchheim, Germany

  • Research Site

    Lübeck, Germany

Israel
  • Research Site

    Ashkelon, Israel

  • Research Site

    Beersheba, Israel

  • Research Site

    Jerusalem, Israel

  • Research Site

    Ramat Gan, Israel

  • Research Site

    Rehovot, Israel

  • Research Site

    Tel Aviv, Israel

Italy
  • Research Site

    Cuneo, Italy

  • Research Site

    Florence, Italy

  • Research Site

    Milan, Italy

  • Research Site

    Milan, Italy

  • Research Site

    Naples, Italy

  • Research Site

    Roma, Italy

  • Research Site

    Torino, Italy

Japan
  • Research Site

    Chiba, Japan

  • Research Site

    Kita-gun, Japan

  • Research Site

    Sagamihara-shi, Japan

  • Research Site

    Sendai, Japan

  • Research Site

    Shinjuku-ku, Japan

United Kingdom
  • Research Site

    Cambridge, United Kingdom

  • Research Site

    Leicester, United Kingdom

  • Research Site

    London, United Kingdom

10 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Benralizumab →Mepolizumab →Placebo to BenralizumabPlacebo to Mepolizumab
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
29 Oct 2019
Primary completion
10 Aug 2023
Completion
30 Nov 2026
Last update posted
12 Aug 2026
Registered enrollment
140
Registry id
NCT04157348

Cross-registrations

EU-CTR / CTIS (EudraCT)2019-001832-77EU-CTR / CTIS (EudraCT)2023-510248-19-00

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.