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TrinetX Study of Hypereosinophilic Syndrome (HES) Without an Identifiable Non-haematological Secondary Cause

TrinetX Study of Hypereosinophilic Syndrome (HES) Without an Identifiable Non-haematological Secondary Cause

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06172751
Enrollment
250
Registered
2023-12-15
Start date
2023-12-15
Completion date
2024-04-26
Last updated
2025-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypereosinophilic Syndrome (HES)

Brief summary

The purpose of this study is to build the knowledge base on clinical characteristics, clinical management, and treatment outcomes of HES.

Detailed description

Retrospective database analysis using TriNetX database to describe HES patient characteristics, journey, and disease burden.

Interventions

OTHERno intervention

not applicable, this is an observational retrospective data analysis study; no interventions in the study

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosis record of HES (ICD-10-CM D72.11) anytime during 01 October 2020 to 30 June 2023 * At least 12 months of patient insurance record prior to first HES record.

Exclusion criteria

* Any mutation in PDGFRA, PDGFRB or FGFR1 genes (to exclude clonal HES). * History of BCR-ABL tyrosine kinase inhibitor use: imatinib, dasatinib, nolitinib, bosutinib, ponatinib, asciminib (to exclude clonal HES) * History of myeloid leukemia, myeloproliferative disorder, myelodysplastic disorder, myelomonocytic leukemia, acute erythroid leukemia, acute megakaryoblastic leukaemia, acute panmyelosis with myelofibrosis, and other specified leukaemias (to exclude reactive HES) * History of helminthiasis or use of anthelmintic medication (to exclude reactive HES) * History of autoimmune disease (to exclude reactive HES) * History of use of specific drugs: antiepileptics, sulfonamides, allopurinol, and immune checkpoint inhibitors (to exclude reactive HES)

Design outcomes

Primary

MeasureTime frameDescription
Number of organ systems with HES signs and/or symptoms01 October 2020 - the most recent data available in 2023To describe the disease burden of HES.
Comorbidities prior to first HES record01 October 2020- the most recent data available in 2023To describe clinical characteristics of patients with HES.
Other eosinophilic conditions01 October 2020- the most recent data available in 2023To describe the clinical characteristics of HES patients.
Organ system with HES signs and/or symptoms01 October 2020- the most recent data available in 2023To describe the disease burden of HES.

Secondary

MeasureTime frameDescription
Demographic characteristics01 October 2020- the most recent data available in 2023To describe the demographic characteristics of HES patients and sub-group analysis patients.
Patient journey in diagnostic phase01 October 2020 - the most recent data available in 2023To describe the patient journey in diagnostic phase and in sub-group analysis.
HES and non-HES therapies & treatment pattern01 October 2020 - the most recent data available in 2023To describe the treatment pattern of HES patients and sub-group analysis patients.
Clinical outcomes01 October 2020 - the most recent data available in 2023To describe clinical outcome pre and post index date and compare between biologics and patients treated with anti-IL-5/IL-5Rα therapies.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026