Clinical Trials Directory

Trials / Completed

CompletedNCT01702623

Crossover Bioequivalence Study of Oxcarbazepine 600 mg Suspension Under Fasted Conditions

A Single Dose, Two-Period, Two-Treatment, Two-Sequence Crossover Bioequivalence Study of Oxcarbazepine 600 mg Suspension Under Fasted Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
64 (actual)
Sponsor
Roxane Laboratories · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to prove the bioequivalence of Roxane Laboratories' Oxcarbazepine Suspension 600 mg under fasted conditions.

Conditions

Interventions

TypeNameDescription
DRUGOxcarbazepine

Timeline

Start date
2009-09-01
Primary completion
2009-09-01
Completion
2009-09-01
First posted
2012-10-08
Last updated
2018-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01702623. Inclusion in this directory is not an endorsement.

Crossover Bioequivalence Study of Oxcarbazepine 600 mg Suspension Under Fasted Conditions (NCT01702623) · Clinical Trials Directory