The specific purpose of this organization is to promote and facilitate research bridging basic scientific research into investigational therapeutics for amyotrophic lateral sclerosis (ALS or Motor Neurone Disease MND). ALS is an invariably fatal disease for which no United States FDA approved treatment is currently regarded as effective at changing short or longterm patient outcomes, to include slowing progression, reversing symptoms, or effectively curing a patient. The Organization will identify novel molecular entities with qualities applicable to ALS and will fund further development with the aim of delivering them into human clinical trial.