Abstract
This paper discusses the development of the partnership between Rhône-Poulenc Rorer (RPR) and two patient groups that are dedicated to the care of patients with amyotrophic lateral sclerosis (ALS) or (Lou Gehrig disease): the ALS Association (ALSA) and the Muscular Dystrophy Association (MDA). This partnership covered the preapproval, approval, and postapproval periods in the drug development of Rilutek® (riluzole), which was approved by the Food and Drug Administration (FDA) to treat patients with ALS in 1995. The partnership between RPR and the patient group associations continues to evolve.
Get full access to this article
View all access options for this article.
