Study identifier:D3254R00004
ClinicalTrials.gov identifier:NCT06172751
EudraCT identifier:N/A
CTIS identifier:N/A
TrinetX Study of Hypereosinophilic Syndrome (HES) without an identifiable non-haematological secondary cause
Hypereosinophilic Syndrome (HES)
N/A
No
-
All
250
Observational
n/a - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Feb 2025 by AstraZeneca
AstraZeneca
-
The purpose of this study is to build the knowledge base on clinical characteristics, clinical management, and treatment outcomes of HES.
Retrospective database analysis using TriNetX database to describe HES patient characteristics, journey, and disease burden.
Location
Location
Cambridge, Massachusetts, United States, 02140
Arms | Assigned Interventions |
---|---|
anti-IL-5/IL-5R therapy Patients initiated anti-IL-5/IL-5R therapy | Other: no intervention not applicable, this is an observational retrospective data analysis study; no interventions in the study |
other therapies Patients initiated other therapies. | Other: no intervention not applicable, this is an observational retrospective data analysis study; no interventions in the study |
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