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Completed Phase 3 Interventional Results available

Evaluation of Efficacy and Safety of OXC XR as Adjunctive Therapy for Partial Seizures

ClinicalTrials.gov ID: NCT00772603

Public ClinicalTrials.gov record NCT00772603. 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 Nov 1, 2026, 5:29 AM EST

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

Official title

Phase III Study to Evaluate the Efficacy and Safety of OXC XR as Adjunctive Therapy in Subjects With Refractory Partial Seizures

Brief summary

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

Evaluation of the safety and efficacy of Oxcarbazepine XR as adjunctive treatment for adults with partial onset seizures

Study identification

NCT ID
NCT00772603
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Supernus Pharmaceuticals, Inc.
Industry
Enrollment
366 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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
Nov 2008 (Type not available)
Primary completion
Apr 2010 (Actual)
Completion
Nov 2010 (Actual)
Last update posted
Feb 11, 2014

2008 – 2010

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
23
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 Atlanta Georgia — —
Not listed Springfield Illinois — —
Not listed Lexington Kentucky — —
Not listed Bethesda Maryland — —
Not listed Missoula Montana — —
Not listed Camden New Jersey — —
Not listed New York New York — —
Not listed Oklahoma City Oklahoma — —
Not listed Philadelphia Pennsylvania — —
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 48 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00772603, 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 Feb 11, 2014 · Synced Nov 1, 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 NCT00772603 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →