Crossover Bioequivalence Study of Oxcarbazepine 600 mg Suspension Under Fed Conditions
Completed · Phase 1
Conditions studied: Seizures
In brief
The objective of this study was to prove the bioequivalence of Roxane Laboratories' Oxcarbazepine Suspension 600 mg under fed conditions
Key facts
- Study ID
- NCT01703468
- Run by
- Roxane Laboratories
- People needed
- 59
- Starts
- 2009-09-01
- Expected to finish
- 2009-10-01
- Last updated by the study team
- 2018-01-23
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening
You may not qualify if…
- Positive test for HIV, Hepatitis B, or Hepatitis C.
- Treatment with known enzyme altering drugs.
- History of allergic or adverse response to oxcarbazepine or any comparable or similar product.
Where it is running
- Worldwide Clinical Trials Drug Development Solutions (formerly CEDRA Clinical Research) — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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