drugset / Trial / NCT02052739

Study to Evaluate SAGE-547 Injection as Adjunctive Therapy for the Treatment of Super-Refractory Status Epilepticus

NCT02052739 ↗

Phase 1/2 Completed 25 enrolled Supernus Pharmaceuticals, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of SAGE-547 in participants in super-refractory status epilepticus (SRSE).

Timeline

Start
2014-03-21
Primary completion
2015-05-03
Completion
2015-05-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Brexanolone Unknown 86 ug/kg Intravenous
Subject Brexanolone Unknown 156 ug/kg Intravenous