Long Term Study of the Safety of OXC XR as in Pediatric Epilepsy Subjects

NCT00918424 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2017-05-09

No results posted yet for this study

Summary

Follow-on study to continue evaluation of the safety of OXC XR as adjunctive therapy in pediatric epilepsy

Conditions

Interventions

DRUG

Oxcarbazepine Extended Release

OXC XR is a once-daily formulation of oxcarbazepine and is given at the same dosage levels.

Sponsors & Collaborators

  • Supernus Pharmaceuticals, Inc.

    lead INDUSTRY

Eligibility

Min Age
4 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00918424 on ClinicalTrials.gov