BenRalizumab Effect on Airway Remodeling in Severe Eosinophilic asTHmatics

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Response to biologic therapies in severe asthma is variable, with patients being either non-responders, responders or super-responders. There is currently no explanation for this broad variation in response. It is important to examine whether these patients have distinct characteristics that could help the treating physician in making the correct diagnosis in clinical practice. Aim of this clinical study is to evaluate the efficacy of benralizumab, a humanized an anti-interleukin 5 receptor α monoclonal antibody in patients with severe eosinophilic asthma and to evaluate airway remodeling before and after benralizumab treatment. Hypothesis Identification of pathological and clinical characteristics in patients with severe eosinophilic asthma after benralizumab treatment regarding the airway remodeling, inflammatory cells, and other biomarkers on a long-term basis. Research questions Is there any improvement in airway remodeling? Are there any biomarkers to predict response to benralizumab treatment in severe eosinophilic asthmatic patients?

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
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• Written informed consent must be obtained at screening visit, before any assessment will be performed. Subjects should be able to provide informed written consent (study participation informed consent form): Able to give written informed consent prior to participation in the study, which will include the ability to comply with the requirements and restrictions listed in the consent form. Subjects must be able to read, comprehend, and write at a level sufficient to complete study related materials.

• Confirmed severe asthma diagnosis and treatment requirements according to American Thoracic Society(ATS)/European Respiratory Society (ERS) guidelines and Global Initiative for Asthma (GINA) 2023.

• Blood eosinophils ≥150cells/ul at screening visit or ≥300cells/ul the last 12 months.

• Patients with history ≥ 1 exacerbation the previous year under the treatment of high dose of inhaled corticosteroid(ICS)+LABA±LAMA or receiving oral/systemic corticosteroids at least 3 days. For subjects on maintenance oral corticosteroids, an exacerbation requiring oral corticosteroids was defined as the use of oral/systemic corticosteroids at least double the existing dose for at least 3 days.

• Meet requirements for biologic therapy with Benralizumab.

Locations
Other Locations
Greece
Pulmonary Clinic, Aristotle University of Thessaloniki, George Papanikolaou Hospital
RECRUITING
Thessaloniki
Contact Information
Primary
Kalliopi Domvri, Dr
kdomvrid@auth.gr
00306940904246
Backup
Konstantinos Porpodis, Ass Prof
kporpodis@yahoo.gr
00306944728818
Time Frame
Start Date: 2024-03-01
Estimated Completion Date: 2026-06-01
Participants
Target number of participants: 45
Treatments
Experimental: Benralizumab Arm A
Benralizumab (30mg) administered subcutaneously every 4 weeks for the first 3 dose and then every 8 weeks.
No_intervention: No intervention Arm B
No intervention. Standard of care as treatment.
Related Therapeutic Areas
Sponsors
Collaborators: University Hospital of Crete, Pulmonary Clinic, Democritus University of Thrace, Pulmonary Clinic, University of Ioannina, 2nd Pulmonary Clinic, Kapodistrian University of Athens, Pulmonary and Respiratory Failure Department, National and Kapodistrian University of Athens, University Hospital of Patras
Leads: Aristotle University Of Thessaloniki

This content was sourced from clinicaltrials.gov