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Completed Phase 1Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT02052739

Public ClinicalTrials.gov record NCT02052739. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 11:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of SAGE-547 Injection as Adjunctive Therapy for the Treatment of Super-Refractory Status Epilepticus

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT02052739
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Supernus Pharmaceuticals, Inc.
Industry
Enrollment
25 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
2 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 21, 2014 (Actual)
Primary completion
May 3, 2015 (Actual)
Completion
May 3, 2015 (Actual)
Last update posted
Sep 15, 2025

2014 – 2015

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Sage Investigational Site Birmingham Alabama 35294 —
Sage Investigational Site Sarasota Florida 34239 —
Sage Investigational Site Chicago Illinois 60611 —
Sage Investigational Site Wichita Kansas 67214 —
Sage Investigational Site New Orleans Louisiana 70121 —
Sage Investigational Site Boston Massachusetts 02114 —
Sage Investigational Site Boston Massachusetts 02115 —
Sage Investigational Site Ann Arbor Michigan 48109 —
Sage Investigational Site Detroit Michigan 48322 —
Sage Investigational Site New York New York 10032 —
Sage Investigational Site Rochester New York 14642 —
Sage Investigational Site Durham North Carolina 27710 —
Sage Investigational Site Winston-Salem North Carolina 27157 —
Sage Investigational Site Philadelphia Pennsylvania 19104 —
Sage Investigational Site Nashville Tennessee 37232 —
Sage Investigational Site Dallas Texas 75251 —
Sage Investigational Site Temple Texas 76504 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02052739, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 15, 2025 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02052739 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →