This is a non-interventional, study to assess demographic characteristics and patient reported outcomes in China patients with SEA treated with benralizumab - SPEED

Study identifier:D3250R00131

ClinicalTrials.gov identifier:NCT06862206

EudraCT identifier:N/A

CTIS identifier:N/A

Will Be Recruiting

Official Title

A multicentre, single arm, non-interventional, prospective study to assess demographic characteristics and patient reported outcomes in patients with severe eosinophilic asthma treated with benralizumab in China

Medical condition

Chronic Obstructive Pulmonary Disease

Phase

N/A

Healthy volunteers

No

Study drug

-

Sex

All

Estimated Enrollment

1000

Study type

Observational

Age

n/a - n/a

Date

Study Start Date: 31 May 2025
Estimated Primary Completion Date: 31 Jan 2026
Estimated Study Completion Date: 31 Jan 2026

Study design

Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Apr 2025 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria