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Completed Phase 2 Interventional

Talampanel for Amyotrophic Lateral Sclerosis (ALS)

ClinicalTrials.gov ID: NCT00696332

Public ClinicalTrials.gov record NCT00696332. 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 Apr 29, 2026, 10:24 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 Multinational, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Assess the Efficacy, Tolerability and Safety of Talampanel in Subjects With Amyotrophic Lateral Sclerosis (ALS)

Study identification

NCT ID
NCT00696332
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
559 participants

Conditions and interventions

Conditions

Interventions

  • Talampanel Drug
  • placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 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
Aug 31, 2008
Primary completion
Mar 31, 2010
Completion
Apr 30, 2010
Last update posted
Oct 20, 2011

2008 – 2010

United States locations

U.S. sites
7
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
CA Medical Center for Movement Disorders-Forbes Norris MDA/ALS Research Center San Francisco California 94115
University of Kansas Medical Center - Dept of Neurology Kansas City Kansas 66160
Johns Hopkins OPC - Meyer Bldg Baltimore Maryland 21287
Massachusetts General Hospital-Neurology Clinical Trials Unit Charlestown Massachusetts 02129
Mayo Clinic Rochester Minnesota 55905
Columbia University - Neurology Institute New York New York 10032
SUNY Upstate Medical University Syracuse New York 13210

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00696332, 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 Oct 20, 2011 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00696332 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →