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Completed Phase 2 Interventional

A Study of NP001 in Subjects With Amyotrophic Lateral Sclerosis (ALS)

ClinicalTrials.gov ID: NCT01281631

Public ClinicalTrials.gov record NCT01281631. 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 Oct 29, 2026, 5:47 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 Phase 2 Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of NP001 in Subjects With Amyotrophic Lateral Sclerosis (ALS)

Brief summary

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

This is a Phase 2 randomized, double-blind, placebo-controlled, multicenter study of NP001 in subjects with ALS.

Study identification

NCT ID
NCT01281631
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Neuraltus Pharmaceuticals, Inc.
Industry
Enrollment
136 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
21 Years to 80 Years
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
Feb 2011 (Type not available)
Primary completion
Sep 2012 (Actual)
Completion
Sep 2012 (Actual)
Last update posted
Nov 22, 2012

2011 – 2012

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Mayo Clinic, Scottsdale Scottsdale Arizona 85259 —
UC, Irvine Irvine California 92868-4281 —
UCLA Los Angeles California 90095 —
California Pacific Med Center Forbes Norris MDA/ALS Research and Treatment Center San Francisco California 94115 —
Mayo Clinic, Jacksonville Jacksonville Florida 32224 —
The Emory Clinic Atlanta Georgia 30322 —
University of Kansas Medical Center, Landon Center on Aging Kansas City Kansas 66160 —
University of Kentucky, Department of Neurology Lexington Kentucky 40536-0284 —
Massachusetts General Hospital Charlestown Massachusetts 02129 —
Columbia University New York New York 10032 —
SUNY Upstate Medical University, Syracuse Syracuse New York 13210 —
Carolinas Medical Center Charlotte North Carolina 28207 —
Duke University, Dept of Neurology Durham North Carolina 27705 —
Cleveland Clinic Cleveland Ohio 44195 —
Providence ALS Center Portland Oregon 97213 —
Methodist Hospital Research Institute, Methodist Neurologic Institute Houston Texas 77030 —
Providence Saint Peter Hospital Centralia Washington 98531 —

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 NCT01281631, 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 Nov 22, 2012 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01281631 live on ClinicalTrials.gov.

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