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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

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