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Bioequivalency Study of Oxcarbazepine 600 mg Tablets Under Fed Conditions
This study has been completed.
Sponsored by: Roxane Laboratories
Information provided by: Roxane Laboratories
ClinicalTrials.gov Identifier: NCT00616863
  Purpose

The objective of this study was to assess the bioequivalence of a potential generic 600 mg oxcarbazepine tablet formulation with Novartis Pharmaceutical's 600 mg oxcarbazepine tablet, Trileptal, folloiwng a single 600 mg dose administered with food.


Condition Intervention
Epilepsy
Seizures
Drug: Oxcarbazepine

Genetics Home Reference related topics: pyridoxal 5'-phosphate-dependent epilepsy pyridoxine-dependent epilepsy
MedlinePlus related topics: Epilepsy Seizures
Drug Information available for: Oxcarbazepine
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Crossover Assignment, Bio-equivalence Study
Official Title: A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Oxcarbazapine 600 mg Tablets Under Fed Conditions

Further study details as provided by Roxane Laboratories:

Primary Outcome Measures:
  • Bioequivalence [ Time Frame: Baseline, two period, 7 day washout ] [ Designated as safety issue: No ]

Enrollment: 28
Study Start Date: July 2004
Study Completion Date: July 2004
Primary Completion Date: July 2004 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • No clinically significant abnormal finding on the physical examination, medical history, or clinical laboratory results during screening.

Exclusion Criteria:

  • Positive test for HIV, Hepatitis B, or Hepatitis C.
  • Treatment with known enzyme altering drugs.
  • History of allergic or advers response to oxcarbazepine or any other comparable or similar product.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00616863

Locations
Canada, Quebec
MDS Pharma Services
Montreal, Quebec, Canada, H4R 2N6
Sponsors and Collaborators
Roxane Laboratories
Investigators
Principal Investigator: Gaetano Morrelli, MD MDS Pharma Services
  More Information

Responsible Party: Roxane Laboratories, Inc. ( Elizabeth Ernst, Director, Drug Regulatory Affairs and Medical Affairs )
Study ID Numbers: OXCA-02
Study First Received: February 4, 2008
Last Updated: February 14, 2008
ClinicalTrials.gov Identifier: NCT00616863  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Oxcarbazepine
Malnutrition
Epilepsy
Seizures
Central Nervous System Diseases
Brain Diseases

Additional relevant MeSH terms:
Therapeutic Uses
Nervous System Diseases
Central Nervous System Agents
Pharmacologic Actions
Anticonvulsants

ClinicalTrials.gov processed this record on January 14, 2009