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Terminated Phase 2 Interventional Results available

The Purpose of This Study is to Determine if Tetrodotoxin (TTX) is Effective in the Treatment of Pain Resulting From Chemotherapy Treatment

ClinicalTrials.gov ID: NCT01655823

Public ClinicalTrials.gov record NCT01655823. 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 23, 2026, 1:18 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 Randomized, Double-Blind, Dose-Finding, Placebo Controlled, Phase II Multicenter Study of Tetrodotoxin in the Treatment of Chemotherapy Induced Neuropathic Pain

Study identification

NCT ID
NCT01655823
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Wex Pharmaceuticals Inc.
Industry
Enrollment
125 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Tetrodotoxin 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
Jun 30, 2012
Primary completion
Dec 31, 2014
Completion
Feb 10, 2015
Last update posted
Oct 29, 2018

2012 – 2015

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Lalita Pandit Fountain Valley California 92708
Robert Moss Fountain Valley California 92708
Alliance Research Centers Laguna Hills California 92653
Global Research Management Los Angeles California 90027
Innovative Clinical Research Los Angeles California 90603
El Camino Cancer Center Mountain View California 94040
Pacific Cancer Care Salinas California 93901
Redwood Regional Medical Group Santa Rosa California 95403
St. Vincent's Medical Center Bridgeport Connecticut 06606
Medsol Clinical Research Center Port Charlotte Florida 33952
Axcess Medical Research Wellington Florida 33414
Cancer Center of Middle Georgia Dublin Georgia 31021
Cancer Center of Kansas Wichita Kansas 67214
Center for Cancer and Blood Disorders Bethesda Maryland 20817
St. Louis Cancer Care Bridgeton Missouri 63044
Mercy Medical Research Institute Springfield Missouri 65807
John Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601
New Mexico Oncology Hematology Consultants Albuquerque New Mexico 87103
Signal Point Clinical Research Center Middletown Ohio 45042
Institute of Pain Research Oklahoma City Oklahoma 73104
Gettysburg Cancer Center Gettysburg Pennsylvania 17325
University of Texas Southwestern Dallas Texas 75390-9179
Jean Brown Research Salt Lake City Utah 84124

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 NCT01655823, 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 Oct 29, 2018 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01655823 live on ClinicalTrials.gov.

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