Study identification

EU PAS number

EUPAS1000000531

Study ID

1000000531

Official title and acronym

Associations between biological and clinical response following treatment with anti-IL5/5R biologics (FLAME)

DARWIN EU® study

No

Study countries

Argentina
Belgium
Brazil
Bulgaria
Canada
Colombia
Denmark
Estonia
France
Greece
India
Ireland
Italy
Japan
Korea, Republic of
Kuwait
Mexico
Norway
Poland
Portugal
Saudi Arabia
Singapore
Spain
Taiwan
United Arab Emirates
United Kingdom
United States

Study description

A registry-based historical cohort study of severe asthma patients who initiated anti-IL5/5R biologic treatments. Changes in clinical outcomes (lung function and exacerbations) and changes in a biomarker (blood eosinophil count) over time following initiation of the biologic will be related to each other and to baseline patient characteristics as well as to other prior and ongoing asthma treatments.
The main aim of the study is to identify patient characteristics associated with biological and/or clinical treatment failure at different times after initiation of anti-IL5/5R biologics and the extent to which these are linked or independent events.
This information will help clinicians in selecting the best treatment for patients and provide important evidence on the information that should be collected before and after biologic initiation.

Study status

Ongoing
Research institutions and networks

Institutions

Contact details

David Price 0000-0002-9728-9992

Primary lead investigator
ORCID number:
0000-0002-9728-9992

Study timelines

Date when funding contract was signed

Planned:
Actual:

Study start date

Planned:
Actual:

Data analysis start date

Planned:

Date of interim report, if expected

Planned:

Date of final study report

Planned:
Sources of funding
Other
Pharmaceutical company and other private sector 

More details on funding

Joint funding from AstraZeneca and Optimum Patient Care Global for data collection. Funding from Optimum Patient Care Global for analysis of the data.
Regulatory

Was the study required by a regulatory body?

No

Is the study required by a Risk Management Plan (RMP)?

Not applicable