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Completed Phase 1 Interventional

A Conversion Study of Immediate Release (IR) and Modified Release (MR) Forms of Topiramate (TPM)

ClinicalTrials.gov ID: NCT01114854

Public ClinicalTrials.gov record NCT01114854. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 4:41 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Conversion Study to Determine the Relative Bioavailability of TPM MR vs TPM IR in Subjects With Epilepsy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This multi-center, two-treatment study compares the pharmacokinetic profiles of Immediate Release (IR) and Modified Release (MR) formulations of Topiramate (TPM) in patients with epilepsy.

Study identification

NCT ID
NCT01114854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Supernus Pharmaceuticals, Inc.
Industry
Enrollment
69 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2010
Primary completion
Nov 30, 2010
Completion
Dec 31, 2010
Last update posted
May 17, 2017

2010 – 2011

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Kyle Patrick Phoenix Arizona 85013
Victor Biton Little Rock Arkansas 72205
Mohammed Bari National City California 91950
Dr. Segal Fort Lauderdale Florida 33308
Dr. Sackellares Gainesville Florida 32607
James Kiely Atlanta Georgia 30342
Bassem El-Nabbout Wichita Kansas 67214
Dr. Chumley Lexington Kentucky 20513
Dr. Fisher Oklahoma City Oklahoma 73112

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01114854, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 17, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01114854 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →