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NOT YET RECRUITING
NCT07371689
PHASE3
ANAKINRA IN THE TREATMENT OF PEDIATRIC ACUTE MYOCARDITIS
Sponsor: Assistance Publique - Hôpitaux de Paris
View on ClinicalTrials.gov
Summary
Double blind RCT aiming to compare the efficacy of Anakinra vs placebo, on top of the standard of care, on restoration of myocardial function at 3 days following treatment initiation, in children admitted for acute myocarditis in intensive care units.
Key Details
Gender
All
Age Range
3 Months - 18 Years
Study Type
INTERVENTIONAL
Enrollment
110
Start Date
2026-02
Completion Date
2029-12
Last Updated
2026-01-28
Healthy Volunteers
No
Conditions
Interventions
DRUG
Anakinra, KINERET®
Patients will be randomized to receive Anakinra 4mg/Kg (maximum 100 mg) subcutaneously once a day for 7 days
Locations (1)
Bicêtre Hospital - APHP, Pediatric intensive care unit
Le Kremlin-Bicêtre, France, France