Clinical Trials Directory

Trials / Completed

CompletedNCT00939705

Bioequivalence Study of Torrent Pharmaceutical Ltd.'s Topiramate Tablets Under Fed Conditions

Study to Evaluate the Bioequivalence of a Test Tablet Formulation of Topiramate (2 x 25 mg), Compared to an Equivalent Dose of a Commercially Available Reference Drug Product (Topamax®, Ortho-McNeil Neurologics, Inc.) in Fed, Healthy, Adult Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Torrent Pharmaceuticals Limited · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

* Objective: * Compare the bioequivalence of a test topiramate formulation (Torrent Pharmaceuticals Limited) to an equivalent oral dose of the commercially available topiramate (Topamax®, Ortho-McNeil Neurologics, Inc.) in a test population of adult subjects under fed conditions. * Clinical Design: * Studies were Randomized, Two-Way Crossover, Single-Dose,Open-Label in healthy human adult subjects.

Conditions

Interventions

TypeNameDescription
DRUGtopiramateTopiramate (brand name Topamax) is an anticonvulsant (antiepilepsy) drug. IUPAC name 2,3:4,5-Bis-O-(1-methylethylidene)-beta-D-fructopyranose sulfamate

Timeline

First posted
2009-07-15
Last updated
2011-10-10
Results posted
2011-10-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00939705. Inclusion in this directory is not an endorsement.