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A Phase III Study to Evaluate the Efficacy and Safety of Benralizumab in Patients With Hypereosinophilic Syndrome (HES)

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NCT04191304 · results posted

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
134actual
Sites
52
Countries
Argentina, Austria, Belgium +14

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2020-07-20actualWhen the study began enrolling
Primary completion2025-05-07actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-02-28estimatedThe whole study's end, after follow-up
First posted2019-12-09actualWhen this record first appeared on the registry
Results posted2026-07-10actualWhen the sponsor posted results to the registry
Record updated2026-07-10actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hypereosinophilic Syndrome

Interventions

  • Biological: Benralizumab
  • Biological: Placebo

Primary outcome

what the primary-completion date above is the date OF
Time to First HES Worsening/Flare During the DB Treatment Period
measured DB period (Baseline to Week 24)

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2024-09-26 · 4.7 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-02-05 · 5.4 MB · SAP_003.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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