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NCT02075255 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety Study of Benralizumab to Reduce OCS Use in Patients With Uncontrolled Asthma on High Dose Inhaled Corticosteroid Plus LABA and Chronic OCS Therapy

A Phase 3 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 3
Development phase
220
Enrollment target

NCT02075255: Completed Phase 3 study, sponsored by AstraZeneca.

NCT02075255 is a Phase 3 study that has completed, run by AstraZeneca. The registered enrollment target is 220 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02075255, a Phase 3 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 3
Development phase
220 participants
Enrollment target

Study Summary

The purpose of this trial is to confirm if benralizumab can reduce the use of maintenance OCS in systemic corticosteroid dependent patients with severe refractory asthma with elevated eosinophils.

Primary Outcome

Baseline OCS dose is the dose upon which the patient is stabilised at randomisation (Week 0). Final OCS dose is the dose at Week 28. The percentage reduction from baseline is defined as: {(Baseline dose-final dose)/baseline dose}\*100%. If a patient discontinues from the study during a given dose reduction period, or the patient experiences an exacerbation between Weeks 24 and 28 or immediately before discontinuation, then the final OCS dose will be 1 dose level higher than that which directly p

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL Benralizumab

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2014-04-28
Est. Completion 2016-08-08
Phase Phase 3
AstraZeneca

1,285 total trials

What the finished NCT02075255 record still lists

NCT02075255 is an interventional study that assigns participants to a tested intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02075255 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02075255 about?

NCT02075255 is a clinical study titled "Efficacy and Safety Study of Benralizumab to Reduce OCS Use in Patients With Uncontrolled Asthma on High Dose Inhaled Corticosteroid Plus LABA and Chronic OCS Therapy". The purpose of this trial is to confirm if benralizumab can reduce the use of maintenance OCS in systemic corticosteroid dependent patients with severe refractory asthma with elevated eosinophils.

What is the current status of trial NCT02075255?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 220 participants. The study started on 2014-04-28. Estimated completion is 2016-08-08.

What interventions are being tested in trial NCT02075255?

The interventions under investigation include: Placebo (BIOLOGICAL), Benralizumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT02075255?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02075255's enrollment target sits among peer trials

220 1318th of 2000 higher than 672 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02075255, the US trial registry maintained by the National Library of Medicine. NCT02075255 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.