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Completed Phase 2 Interventional

Study of NNZ-2566 in Patients With Traumatic Brain Injury

ClinicalTrials.gov ID: NCT00805818

Public ClinicalTrials.gov record NCT00805818. 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 Sep 2, 2026, 10:06 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 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study of NNZ-2566 in Patients With Traumatic Brain Injury

Brief summary

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

The purpose of this study is to determine whether NNZ-2566 is safe and effective in the treatment of Traumatic Brain Injury (TBI).

Study identification

NCT ID
NCT00805818
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Neuren Pharmaceuticals Limited
Industry
Enrollment
261 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
Male
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
Mar 31, 2010
Primary completion
Dec 31, 2015
Completion
Dec 31, 2015
Last update posted
Feb 4, 2018

2010 – 2016

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
University of South Alabama Mobile Alabama 36617
University of Arizona Tucson Arizona 85724
Arrowhead Regional Medical Center Colton California 92324
Ronald Reagan UCLA Medical Center Los Angeles California 90095
University of California, Davis Medical Center Sacramento California 95817
University of Miami, Lois Pope Life Center Miami Florida 33136
The Queen's Medical Center Honolulu Hawaii 96813
Our Lady of the Lake Hospital Baton Rouge Louisiana 70808
Detroit Receiving Hospital and University Health Center Detroit Michigan 48201
Sinai Grace Hospital Detroit Michigan 48235
Bronson Methodist Hospital Kalamazoo Michigan 49007
SUNY Upstate Medical University Syracuse New York 13210
University of Cincinnati, Mayfield Clinic Cincinnati Ohio 45219
Miami Valley Hospital Dayton Ohio 45409
St Luke's University Hospital Bethlehem Pennsylvania 18015
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213
Texas Health Harris Methodist Hospital Fort Worth Fort Worth Texas 76104
Inova Fairfax Hospital Falls Church Virginia 22042
Charleston Area Medical Center Charleston West Virginia 25304
University of Wisconsin, Froedtert Hospital Milwaukee Wisconsin 53226

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 NCT00805818, 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 Feb 4, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00805818 live on ClinicalTrials.gov.

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