Study identifier:D3250R00099
ClinicalTrials.gov identifier:NCT05180357
EudraCT identifier:N/A
CTIS identifier:N/A
Retrospective, Observational Study in Patients with Severe Eosinophilic Asthma and Nasal Polyps treated by FASENRA®
Severe Eosinophilic Asthma
N/A
No
-
All
252
Observational
N/A
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2022 by AstraZeneca
AstraZeneca
-
The purpose of this observational study is to describe the population of patients with SEA + NP who have been prescribed FASENRA and assess available clinical outcomes for both NP and asthma.
In light of the increasing importance of comorbidities in driving choice for biologics in severe asthma there is a knowledge gap to understand SEA patients with comorbid NP for whom the decision to start biologics was based on the presence of severe, uncontrolled asthma. This retrospective, observational study will describe the population of patients with SEA + NP who have been prescribed FASENRA and assess available clinical outcomes for both NP and asthma.
Location
Location
Rochester, NY, United States, 14642
Location
Wiesbaden, Germany, 65183
Location
Catanzaro, Italy, 88100
Location
Salerno, Italy, 84131
Location
Rome, Italy, 00161
Location
Monserrato, Italy, 09042
Location
Marseille, France, 13015
Location
Napoli, Italy, 80131
Arms | Assigned Interventions |
---|---|
SEA+NP Patients on FASENRA (benralizumab) SEA+NP Patients on FASENRA (benralizumab) | - |
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