Patient-Reported OUTcomes of Benralizumab in Real-World Use in Severe EosiNophilic Asthma Patients

NCT ID: NCT05603845

Last Updated: 2025-05-09

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 291 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-02-20
• Study Completion Date: 2025-04-10

Brief Summary

This study aims to generate real-world data on the characteristics of patients receiving benralizumab to assess early PRO parameters as well as long-term treatment effects in the Gulf cooperative council (Kingdom of Saudi Arabia, Kuwait, United Arab Emirates, Oman, and Qatar), Latin America (Brazil, Argentina, and Colombia), and India. It is anticipated that the data generated will provide practical, patient-focused real-world evidence and enhance communications between patients and physicians in an objective and structured manner to ensure better disease control in patients under benralizumab treatment.

Detailed Description

This is a multi-country, multi-center, observational, prospective study involving primary data collection within real-world pulmonary care settings for patients who receive benralizumab treatment for severe uncontrolled eosinophilic asthma.The decision by the physician to start benralizumab is made independently from study inclusion and patient informed consent. Patients will receive benralizumab injections according to the local label in the participating countries (Brazil, Argentina, Colombia, India, and the Gulf cooperative council, including the Kingdom of Saudi Arabia, United Arab Emirates, Kuwait, Oman, and Qatar). No study drug will be provided as part of the study. The entire study period duration will be 56 weeks for each subject. The study is anticipated to run for approximately 18 months and is not anticipated to exceed 24 months. A database soft lock is planned at the end of the initial 8-week period of the study, and one combined descriptive and analytical interim analysis will be performed when 50% of the enrolled subjects complete the 8-week follow-up.

Conditions

Severe Asthma

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

1. Male or female patients aged 18 years or older with a physician's confirmed diagnosis of severe eosinophilic, uncontrolled asthma.

2. Severe uncontrolled eosinophilic asthma requiring high-dose* inhaled corticosteroid plus long-acting β adrenoceptor agonist as maintenance treatment.

3. Patients who have been prescribed but not yet initiated treatment with benralizumab (Fasenra®) according to local approved prescribing information prior to signed informed consent.

4. Provision of the signed written informed consent form (ICF) indicating that they understand the purpose of the study and procedures required for participation.

5. Patients must be able and willing to read and comprehend written instructions and complete the paper PRO questionnaires required by the protocol.

Exclusion Criteria

1. Clinically important pulmonary diseases other than asthma including chronic obstructive pulmonary disease (as the main diagnosis), bronchiectasis, idiopathic pulmonary fibrosis, pulmonary hypertension, alpha-1-antitrypsin-deficiency, and malignancy of any kind (NB: the following conditions are permitted: nasal polyposis, allergic rhinitis, atopic dermatitis, non-idiopathic pulmonary fibrosis).

2. Currently enrolled in an interventional clinical study except patients being in parallel documented in a national asthma registry

3. An acute or chronic condition that, in the investigator's opinion, would limit the patients' ability to complete questionnaires or participate in this study or impact the interpretations of results.

4. Concurrent biologics for asthma are not allowed. Acceptable wash-out periods for other asthma biologics: ≥30 days from the last dose of the previous biologic.

5. Women who are currently pregnant, breastfeeding, or lactating

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

AstraZeneca

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Research Site

Bogotá, , Colombia

Research Site

Bucaramanga, , Colombia

Research Site

Ibagué, , Colombia

Research Site

Pereira, , Colombia

Research Site

Santiago de los Caballeros, , Dominican Republic

Research Site

Santo Domingo, , Dominican Republic

Research Site

Ahmedabad, , India

Research Site

Ajmer, , India

Research Site

Chennai, , India

Research Site

Delhi, , India

Research Site

Hyderabad, , India

Research Site

Jaipur, , India

Research Site

Kolkata, , India

Research Site

Pune, , India

Research Site

Secundrabad, , India

Research Site

Vadodara, , India

Research Site

Sabah Al Salem, , Kuwait

Research Site

Muscat, , Oman

Research Site

Doha, , Qatar

Research Site

Jeddah, , Saudi Arabia

Research Site

Riyadh, , Saudi Arabia

Research Site

Abu Dhabi, , United Arab Emirates

Research Site

Al Ain City, , United Arab Emirates

Research Site

Dubai, , United Arab Emirates

Countries

Colombia; Dominican Republic; India; Kuwait; Oman; Qatar; Saudi Arabia; United Arab Emirates

Other Identifiers

D3250R00113

Identifier Type: -

Identifier Source: org_study_id