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CompletedNCT00542412Updated Oct 11, 2007

CARE Canadian ALS Riluzole Evaluation

A Phase 4 interventional study of Riluzole in Amyotrophic Lateral Sclerosis, sponsored by Sanofi. Completed at 1 site in Canada. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2007-10-11.

Sponsored by Sanofi · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
414
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Evaluate the efficacy of riluzole 50-mg bid defined by comparing the percentage of riluzole-treated subjects who experienced death, permanently assisted ventilation (PAV) or tracheostomy, to a group of recent historical controls for the treatment of amyotrophic lateral sclerosis (ALS).

02

Conditions studied

  • Amyotrophic Lateral Sclerosis
03

In context

Motor Neuron Disease

717 studies on the registry are indexed under Motor Neuron Disease; 137 are open to participants now.

This study's enrollment of 414 is above the median of 35 across 461 interventional studies indexed under Motor Neuron Disease.

Browse Motor Neuron Disease studies →

Lead sponsor

Sanofi is the lead sponsor of 1,508 studies on the registry; 90 are open to participants now.

Of its 198 completed or terminated interventional studies of FDA-regulated products, 118 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of ALS confirmed by the following definition:

    (a)"Probable" or "Definite" Amyotrophic Lateral Sclerosis (ALS) according to the El Escorial criteria(b)"Peripheral" onset form (limb involvement) or a "Bulbar" form of ALS with a duration of five years, based on inquiry for the earliest symptoms of the disease

  • A subject who simultaneously presents with bulbar and peripheral signs at onset of ALS disease should be stratified to the bulbar onset group. The neurologic progression of such subjects matches that of the bulbar onset ALS subjects.
  • Pulmonary Function: forced vital capacity (FVC) must be 3 60% at study entry.
  • Females of childbearing potential must be documented to be using acceptable birth control methods such as an IUD or oral contraceptives.

Exclusion criteria

Exclusion Criteria:

  • Previous treatment with riluzole
  • Tracheostomy, or expected to undergo a tracheostomy within two months after study inclusion
  • Signs of clinical dementia and/or major psychiatric disorders
  • Serious concomitant disease or handicap likely to interfere with the subject's assessments or impact on the subject's survival
  • A multiple conduction block has been shown on nerve conduction studies by electromyogram

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

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Study design

Phase
Phase 4
Primary purpose
Treatment
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
414 participants (actual)

Interventions

  • DrugRiluzole
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What researchers measure

Primary outcomes

  1. The primary efficacy endpoint was the time to the occurrence of an ALS-related event (PAV, tracheostomy or ALS-related death)

07

Study locations

1 site
  • Sanofi-Aventis
    Laval, Quebec, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 11, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00542412
Lead sponsor
Sanofi
First posted
Oct 11, 2007
Start date
Jan 2001
Completion
Dec 2004
Last update
Oct 11, 2007

Study contacts

Laurent-Didier Jacobs
study director · Sanofi

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2007. You cannot join it, but the record below documents what was studied.

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