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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 Nov 9, 2026, 11:34 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. 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

Brief summary

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

This study will compare Z160 and placebo in patients with Lumbosacral Radiculopathy for safety and efficacy for a period of 6 weeks.

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

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
Aug 2012 (Type not available)
Primary completion
Oct 2013 (Actual)
Completion
Nov 2013 (Actual)
Last update posted
Dec 12, 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 12, 2013 · Synced Nov 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01655849 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →