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Completed Phase 2 Interventional

Efficacy, Tolerability, and Safety of NXN-462 in Patients With Post-Herpetic Neuralgia

ClinicalTrials.gov ID: NCT01748877

Public ClinicalTrials.gov record NCT01748877. 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 22, 2026, 3:40 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 Double-Blind, Randomized, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Tolerability, and Safety of NXN-462 in Patients With Post-Herpetic Neuralgia (PHN)

Study identification

NCT ID
NCT01748877
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
NeurAxon Inc.
Industry
Enrollment
188 participants

Conditions and interventions

Interventions

  • NXN-462 Drug
  • Placebo 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
Dec 31, 2012
Primary completion
May 31, 2014
Completion
May 31, 2014
Last update posted
Jun 18, 2014

2013 – 2014

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Premier Research Phoenix Arizona 85027
University of Southern California Los Angeles California 90033
Northern California Research Sacramento California 95821
Neurological Research Institute Santa Monica California
Meridien Research Brooksville Florida 34601
FPA Clinical Research Kissimmee Florida 34741
Suncoast Clinical Research New Port Richey Florida
Compass Research LLC Orlando Florida 32806
Meridien Research Tampa Florida 33606
Medex Healthcare Research, Inc. Chicago Illinois 60602
Integrated Clinical Trial Services West Des Moines Iowa
IRC Clinics Towson Maryland 21204
Boston Clinical Trials Boston Massachusetts 02131
Michigan Head-Pain and Neurological Institute Ann Arbor Michigan
Albuquerque Clinical Trials, Inc Albuquerque New Mexico 87102
Clinical Trials of America, Inc. Hickory North Carolina 01845
Lynn Health Science Institute Oklahoma City Oklahoma 73112
Pain Specialist of Charleston, P.A. Mt. Pleasant South Carolina
Nashville Neuroscience Group Nashville Tennessee 37203
Trinity Clinical Research Tullahoma Tennessee 37388
ClinRx Research LLC Plano Texas 75080
Progressive Clinical Research San Antonio Texas

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01748877, 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 Jun 18, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01748877 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →