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Completed Phase 2 Interventional Results available

A Clinical Study in Subjects With Neuropathic Pain From PHN Who Have Had an Inadequate Response to Gabapentin Treatment

ClinicalTrials.gov ID: NCT00617461

Public ClinicalTrials.gov record NCT00617461. 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 Jul 21, 2026, 6:04 PM EDT

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

Official title

Study PXN110527: The Investigation of the Efficacy and Pharmacokinetics of XP13512 in Subjects With Neuropathic Pain Associated With Post-herpetic Neuralgia (PHN) Who Have Had an Inadequate Response to Gabapentin Treatment.

Study identification

NCT ID
NCT00617461
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
XenoPort, Inc.
Industry
Enrollment
96 participants

Conditions and interventions

Interventions

  • GEn 1200mg/day Drug
  • GEn 3600mg/day Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Feb 29, 2008
Primary completion
Jun 30, 2009
Completion
Jun 30, 2009
Last update posted
Jul 21, 2013

2008 – 2009

United States locations

U.S. sites
42
U.S. states
18
U.S. cities
39
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85016
GSK Investigational Site Oxnard California 93030
GSK Investigational Site Roseville California 95661
GSK Investigational Site San Francisco California 94109
GSK Investigational Site Bradenton Florida 34209
GSK Investigational Site Chipley Florida 32428
GSK Investigational Site Daytona Beach Florida 32117
GSK Investigational Site Fort Myers Florida 33916
GSK Investigational Site Gainesville Florida 32608
GSK Investigational Site Marianna Florida 32446
GSK Investigational Site Miami Springs Florida 33166
GSK Investigational Site Naranja Florida 33032
GSK Investigational Site South Miami Florida 33143
GSK Investigational Site Tallahassee Florida 32308
GSK Investigational Site Tampa Florida 33603
GSK Investigational Site Tampa Florida 33612
GSK Investigational Site Decatur Georgia 30033
GSK Investigational Site Marietta Georgia 30060
GSK Investigational Site Chicago Illinois 60617
GSK Investigational Site Terre Haute Indiana 47802
GSK Investigational Site Kansas City Missouri 64111
GSK Investigational Site St Louis Missouri 63117
GSK Investigational Site Missoula Montana 59808
GSK Investigational Site Lebanon New Hampshire 03766
GSK Investigational Site New York New York 10004
GSK Investigational Site Greensboro North Carolina 27408
GSK Investigational Site Salisbury North Carolina 28144
GSK Investigational Site Winston-Salem North Carolina 27103
GSK Investigational Site Norman Oklahoma 73071
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Medford Oregon 97501
GSK Investigational Site Greensburg Pennsylvania 15601
GSK Investigational Site Kingsport Tennessee 37660
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Houston Texas 77028
GSK Investigational Site Houston Texas 77044
GSK Investigational Site Houston Texas 77089
GSK Investigational Site Longview Texas 75605
GSK Investigational Site San Antonio Texas 78238
GSK Investigational Site Weber City Virginia 24290
GSK Investigational Site Tacoma Washington 98405
GSK Investigational Site Yakima Washington 98902

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00617461, 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 Jul 21, 2013 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00617461 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →