drugset / Trial / NCT03224585

Treatment of Acute Pericarditis With Anakinra

NCT03224585 ↗

Phase 2 Terminated 5 enrolled Virginia Commonwealth University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this study is to determine the safety and efficacy of anakinra for the treatment of acute pericarditis when initiated within 6 hours of diagnosis and continued for 3 or 7 days. 1. to determine the efficacy of anakinra with respect to chest pain resolution 2. to determine the safety of anakinra with respect to adverse drug events

Timeline

Start
2018-05-11
Primary completion
2020-02-01
Completion
2020-02-01

Outcome

Outcome not reported

Stopped (Enrollment): “Study was terminated because dramatic benefits seen during the first 24 hours of drug administration combined with COVID restrictions on research activities suggested it was both unethical and unnecessary to complete the planned enrollment”

Drugs

EvaluationDrugModalityDoseRoute
Subject Anakinra Protein / enzyme biologic 100 mg Subcutaneous

Indications