ClinicalTrials.gov record
Completed Phase 2 Interventional

Phase 2 Efficacy Trial of Z160 in Lumbosacral Radiculopathy

ClinicalTrials.gov ID: NCT01655849

Public ClinicalTrials.gov record NCT01655849. 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 May 19, 2026, 7:10 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

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate The Efficacy and Safety of Z160 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy

Study identification

NCT ID
NCT01655849
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Zalicus
Industry
Enrollment
141 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • z160 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
Jul 31, 2012
Primary completion
Sep 30, 2013
Completion
Oct 31, 2013
Last update posted
Dec 11, 2013

2012 – 2013

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Investigative Site Huntsville Alabama 35801
Investigative Site Peoria Arizona 85381
Investigative Site Anaheim California 92804
Investigative Site Fresno California 93726
Investigative Site Orange California 92868
Investigative Site Sacramento California 95821
Investigative Site Clearwater Florida 33756
Investigative Site Clearwater Florida 33765
Investigative Site Orlando Florida 32806
Investigative Site Pinellas Park Florida 33781
Investigative Site Plantation Florida 33317
Investigative Site Royal Palm Beach Florida 33411
Investigative Site Atlanta Georgia 30342
Investigative Site Overland Park Kansas 66210
Investigative Site Shreveport Louisiana 71105
Investigative Site Boston Massachusetts 02135
Investigative Site Hazelwood Missouri 63042
Investigative Site Las Vegas Nevada 89144
Investigative Site Medford Oregon 97504
Investigative Site Duncansville Pennsylvania 16635
Investigative Site Dallas Texas 75230
Investigative Site Sandy City Utah 84070
Investigative Site Bellevue Washington 98007

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 NCT01655849, 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 Dec 11, 2013 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01655849 live on ClinicalTrials.gov.

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