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Completed Phase 2 Interventional

Combination Therapy Selection Trial in Amyotrophic Lateral Sclerosis

ClinicalTrials.gov ID: NCT00355576

Public ClinicalTrials.gov record NCT00355576. 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, 11:46 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

Phase II Combination Therapy Selection Trial in Amyotrophic Lateral Sclerosis

Brief summary

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

The objective of this study is to compare two combinations of drugs, minocycline and creatine or celecoxib and creatine, in a phase II trial designed to determine which combination is more effective for ALS.

Study identification

NCT ID
NCT00355576
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Columbia University
Other
Enrollment
86 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years to 85 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
Jun 30, 2006
Primary completion
Not listed
Completion
Apr 30, 2007
Last update posted
Jan 31, 2011

2006 – 2007

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
Phoenix Neurological Associates Phoenix Arizona 85006
UCLA Los Angeles California 90095
University of California Irvine Orange California 92868
California Pacific Medical Center San Francisco California 94115
Mayo Clinic Florida Jacksonville Florida 32224
Medical College of Georgia Augusta Georgia 30912
University of Illinois Chicago Illinois 60637
University of Kansas Kansas City Kansas 66160
Mayo Clinic Rochester Rochester Minnesota 55905
Washington University St Louis Missouri 63110
UMDNJ New Brunswick New Jersey 08901
University of New Mexico Albuquerque New Mexico 87131
Beth Israel New York New York 10003
Columbia University New York New York 10032
Duke University Durham North Carolina 27705
Oregon Health and Science University Portland Oregon 97201
University of Pennsylvania Philadelphia Pennsylvania 19107
UT Southwestern Medical Center Dallas Texas 75390
University of Vermont Burlington Vermont 05405

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 NCT00355576, 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 Jan 31, 2011 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00355576 live on ClinicalTrials.gov.

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