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 May 2024 by AstraZeneca
AstraZeneca
-
No locations available
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 |