drugset / Trial / NCT05611710

Anakinra in Dengue With Hyperinflammation ( AnaDen )

NCT05611710

RandomizedSequentialDouble-blindTreatment

Summary

This study aims to evaluate the effect of anakinra in dengue patients with hyperinflammation as compared to placebo Primary Objective: To evaluate the efficacy of Anakinra in moderate-severe dengue patients with hyperinflammation. Secondary Objectives: * To assess the safety of anakinra therapy in dengue with hyperinflammation * To assess the effect of anakinra therapy in patients with dengue on physiological, clinical and virological parameters * To assess the immunomodulation effects of anakinra in dengue * Immune cell signatures in dengue with and without anakinra * To assess difference in gene expression between treatment group compared to non-treatment population

Timeline

Start
2023-01-02
Primary completion
2025-10-20
Completion
2027-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Anakinra Protein / enzyme biologic 2 mg/kg Intravenous
Subject Anakinra Protein / enzyme biologic 200 mg Intravenous