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ABPAPhase 4NCT04108962

Benralizumab in the Treatment of Patients With Severe Asthma With ABPA

A Phase 4 study testing Fasenra, 30 Mg/mL Subcutaneous Solution in people with ABPA and Severe Asthma, run by Baylor Research Institute at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

Phase IV, open-label study will evaluate effects of Benralizumab in the treatment of severe asthma in patients with allergic bronchopulmonary aspergillosis Read more about this study

Who is it for?
Ages 18 to 75 years
What is being tested?
Fasenra, 30 Mg/mL Subcutaneous Solution
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
1 siteUnited States
Study dates
23 Dec 2019to 1 Oct 2021
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

SELECT INCLUSION CRITERIA

  • Female and Male patients aged 18-75 years inclusively at the time of Visit 1 with a physician diagnosis of Allergic Bronchopulmonary Aspergillosis has met the ISHAM Working Group Diagnostic Criteria for ABPA:
  • Predisposing condition: Bronchial asthma
  • Obligatory criteria (both should be present)
  • Type I aspergillus skin test positive (immediate cutaneous hypersensitivity Aspergillus antigen) or elevated IgE level against Aspergillus fumigatus (Af)
  • Aspergillus niger or Aspergillus flavus may be eligible provided antigen-specific IgE and IgG measurements are available for use.
  • Elevated total IgE levels (>1,000IU/mL)*
  • Other criteria (at least two of three)
  • Presence of precipitating or IgG antibodies against Af in serum
  • Radiographic pulmonary opacities consistent with ABPA
  • Total eosinophil count >500 cells/uL in steroid naïve patients (may be historical)
  • (if the patient meets all other criteria, an IgE value <1,000 IU/mL may be acceptable)
  • Severe chronic asthma (for at least 12 months) requiring treatment with high dose ICS plus asthma controller prior to Visit 1
  • Other acceptable asthma controllers include long acting bronchodilators (e.g. a long acting beta-agonist (LABA) or long-acting muscarinic antagonists (LAMA)), a leukotriene inhibitor, theophylline preparations and/or maintenance OCS (daily or every other day OCS requirement in order to maintain asthma control
  • Documented current treatment with high daily doses of ICS ( >500ug of FP equivalent) plus at least one other asthma controller for at least 3 months prior to Visit 1
  • For ICS/LABA combination preparation, highest-strength maintenance doses approved in the U.S. will meet this criterion
  • If the ICS and the other asthma controller therapies are given by separate inhalers, then the patient must be on a high daily ICS dose for 3 months prior to entering the study.
  • History of at least 2 asthma exacerbations while on ICS plus another asthma controller (see inclusion criterion 2 for examples) that required treatment with systemic corticosteroids (IM, IV, or oral) in the 12 months prior to Visit 1. For patients receiving oral corticosteroids as a maintenance therapy, an exacerbation is defined as a temporary increase of their maintenance dose for a minimum of 3 days.
  • Weight > 40kg

SELECT EXCLUSION CRITERIA

  • Clinical important pulmonary disease other than asthma with allergic bronchopulmonary aspergillosis (ie. chronic obstructive pulmonary disease (COPD), cystic fibrosis, sarcoid, and pulmonary fibrosis)
  • History of anaphylaxis to any biologic therapy
  • Known history of allergy or hypersensitivity reaction to benralizumab or any of its components
  • Current smokers or former smokers with a smoking history of > 10 pack years. A former smoker is defined as a patient who quit smoking at least 6 months prior to Visit 1.
  • Currently pregnant, breastfeeding, or lactating women
  • Concurrent enrollment in another interventional or post-authorization safety study, unless it is observational.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Baylor University Medical Center

    Dallas, Texas, 75246

Other trials in United States

About this study

Official title: Phase IV, Single-Center, Open-Label Study Evaluating the Effects of an Anti-IL5 Receptor Alpha (Benralizumab) Monoclonal Antibody in the Treatment of Severe Asthma in Patients With Allergic Bronchopulmonary Aspergillosis

Phase IV, open-label study will evaluate effects of Benralizumab in the treatment of severe asthma in patients with allergic bronchopulmonary aspergillosis

Read the detailed description

Subjects who have been identified to have severe asthma with ABPA will be consented and enrolled in the study to receive benralizumab injections administered every 4 weeks for the first 3 injections with an additional injection eight weeks to follow for a total of 16 weeks active treatment with a follow-up/termination visit eight weeks from the last injection. The termination visit will occur week 24 for subjects who complete the study treatment. Subjects who receive the first dose of benralizumab but withdraw from the study or terminate study treatment for any reason should complete all the procedures outlined for the termination visit.

Being tested
Fasenra, 30 Mg/mL Subcutaneous Solution
Keywords
ABPA, Benralizumab
Medical subject headings
Asthma, Aspergillosis, Allergic Bronchopulmonary

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Fasenra, 30 Mg/mL Subcutaneous SolutionDrug

    Also called Benralizumab

    Anti-IL5 receptor alpha monoclonal antibody

Study groups in NCT04108962
Study groupRoleWhat they receive
TreatmentExperimentalBenralizumab treatment will be given by injections administered every 4 weeks for the first 3 injections with an additional injection eight weeks to follow for a total of 16 weeks active treatment
Receives: Drug: Fasenra, 30 Mg/mL Subcutaneous Solution

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of steroid requiring exacerbations

    Number of asthma exacerbations requiring the initiation of (or temporary increase in) systemic corticosteroids in severe asthma complicated by ABPA

    Measured: 26 Weeks

Secondary outcomes (3)
  1. Patient-Reported Quality of Life as assessed by Saint George Respiratory Questionnaire

    The change from baseline score in Saint George Respiratory Questionnaire

    Measured: 26 Weeks

  2. Asthma Control as assessed by Asthma Control Questionnaire 6

    The change from baseline score in Asthma Control Questionnaire 6

    Measured: 26 Weeks

  3. Lung Function (FEV1)

    The FEV1 change from baseline to End of Treatment

    Measured: 26 Weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Sep 2019
  2. Study start23 Dec 2019
  3. Primary completion24 Sep 2021
  4. Study completion1 Oct 2021

Why it stopped: Difficult to find eligible patients willing to participate.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04108962
Sponsor's protocol ID
019-294
Status last verified
Jan 2022
First submitted
24 Sep 2019
Last updated
1 Feb 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: no subjects enrolled

Publications

  • Kao CC, Hanania NA, Parulekar AD. The impact of fungal allergic sensitization on asthma. Curr Opin Pulm Med. 2021 Jan;27(1):3-8. doi: 10.1097/MCP.0000000000000740.

    PubMed 33027187

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Fasenra, 30 Mg/mL Subcutaneous Solution in people with ABPA and Severe Asthma, run by Baylor Research Institute at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 1 Feb 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of steroid requiring exacerbations (time frame: 26 Weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04108962, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Feb 2022.

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