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anti-IL-5/IL-5R therapy for Hypereosinophilic Syndrome
N/A
Recruiting
Research Sponsored by AstraZeneca
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 01 october 2020 - the most recent data available in 2023
Awards & highlights
Study Summary
The purpose of this study is to build the knowledge base on clinical characteristics, clinical management, and treatment outcomes of HES.
Eligible Conditions
- Hypereosinophilic Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 01 october 2020- the most recent data available in 2023
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~01 october 2020- the most recent data available in 2023
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Comorbidities prior to first HES record
Number of organ systems with HES signs and/or symptoms
Organ system with HES signs and/or symptoms
+1 moreSecondary outcome measures
Clinical outcomes
Demographic characteristics
HES and non-HES therapies & treatment pattern
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: other therapiesExperimental Treatment1 Intervention
Patients initiated other therapies.
Group II: anti-IL-5/IL-5R therapyExperimental Treatment1 Intervention
Patients initiated anti-IL-5/IL-5R therapy
Find a Location
Who is running the clinical trial?
AstraZenecaLead Sponsor
4,259 Previous Clinical Trials
288,593,652 Total Patients Enrolled
2 Trials studying Hypereosinophilic Syndrome
140 Patients Enrolled for Hypereosinophilic Syndrome
Frequently Asked Questions
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