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Clinical Trials in China / NCT07257835
Recruiting

Dupilumab Therapy for EGIDs

NCT07257835 · tracked via the Priya Life Science China tracker
Sponsor
Children's Hospital of Fudan University
Phase
Started
2025-01-01
Last updated
2025-12-02

Condition(s) studied

Eosinophilic Gastrointestinal Disorders (EGIDs)

Investigational drug(s) / intervention(s)

Dupilumab - Standard Dosesubcutaneous injection

Dupilumab - Standard Dose: Dose: For patients with weight ≥ 15kg but \< 30kg, take 200mg each time, every two weeks; for those with weight ≤ 30kg but \< 60kg, take 300mg each time, every two weeks; for those with weight ≥ 60kg, take 300mg each time, once a week.

subcutaneous injection: Dose: For patients with weight ≥ 15kg but \< 30kg, take 200mg each time, every two weeks; for those with weight ≤ 30kg but \< 60kg, take 300mg each time, every two weeks; for those with weight ≥ 60kg, take 300mg each time, once a week.

Study summary

This is a single-center observational study to investigate the efficacy and tolerability of dupilumab in children with refractory eosinophilic gastrointestinal disorders.

Eligibility

Sex
ALL
Min age
1 Year
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Clinical diagnosis of Refractory Peptic Ulcers * with Refractory Eosinophilic Gastrointestinal Disorders Exclusion Criteria: * with Active Helicobacter pylori infection at present. * with Inflammatory bowel disease * with Parasite infection * with Cancer

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
201102 Shanghai China Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07257835 on ClinicalTrials.gov ↗ ← All trials in China