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Completed Phase 3 Interventional Results available

Safety and Tolerability of OXC XR as Adjunctive Therapy in Subjects With Refractory Partial Epilepsy

ClinicalTrials.gov ID: NCT00908349

Public ClinicalTrials.gov record NCT00908349. 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 27, 2026, 5:11 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

Multicenter, Open-Label Extension Study to Evaluate the Long-Term Safety and Tolerability of OXC XR as Adjunctive Therapy in Subjects With Refractory Partial Epilepsy

Brief summary

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

Open-Label Extension Study to Evaluate the Long-Term Safety and Tolerability of Oxcarbazepine Extended-Release (OXC XR)

Study identification

NCT ID
NCT00908349
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Supernus Pharmaceuticals, Inc.
Industry
Enrollment
214 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 66 Years
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
Jun 2009 (Type not available)
Primary completion
Nov 2011 (Actual)
Completion
Nov 2011 (Actual)
Last update posted
May 31, 2017

2009 – 2011

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Not listed Huntsville Alabama — —
Not listed Northport Alabama — —
Not listed Phoenix Arizona — —
Not listed Tucson Arizona — —
Not listed Little Rock Arkansas — —
Not listed Riverside California — —
Not listed West Los Angeles California — —
Not listed Aurora Colorado — —
Not listed Jacksonville Florida — —
Not listed Miami Florida — —
Not listed Sarasota Florida — —
Not listed Springfield Illinois — —
Not listed Lexington Kentucky — —
Not listed Bethesda Maryland — —
Not listed Missoula Montana — —
Not listed New York New York — —
Not listed Oklahoma City Oklahoma — —
Not listed Nashville Tennessee — —
Not listed Baytown Texas — —
Not listed Temple Texas — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00908349, 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 May 31, 2017 · Synced Oct 27, 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 NCT00908349 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →