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Extension Study of Talampanel for Amyotrophic Lateral Sclerosis (ALS) — ALSTAR OL  

Amyotrophic Lateral Sclerosis Clinical Trial

Official title:
A Multinational, Multicenter, Open Label Phase to Assess Tolerability and Safety of Talampanel 50mg Tid in Subjects With Amyotrophic Lateral Sclerosis (ALS)

Clinical Trial Summary

This will be an open label treatment extension phase in patients with ALS who have previously participated in the double blind, placebo-controlled ALS-TAL-201 study. This study will make talampanel treatment available to all subjects who completed the double blind placebo-controlled phase of ALS-TAL-201 study and where the investigator and patient consider it to be in the patient's interest to receive talampanel 50mg three times daily (tid). It will also enable the exploration of long-term safety and tolerability of talampanel 50mg tid.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00982150
Study type Interventional
Source Teva Pharmaceutical Industries
Contact
Status Terminated
Phase Phase 2
Start date September 2009
Completion date June 2010
View Details
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