ALS Therapy Development Foundation

ALS Therapy Development Foundation thumbnail
There is currently little therapy and no cure for ALS.

The ALS Therapy Development Foundation changed its name to the ALS Therapy Development Institute in 2007, after receiving a major grant and research partnership from the Muscular Dystrophy Association's Augie's Quest. Founded in 1999, ALS TDI was the world's first nonprofit biotechnology company.

  1. Amyotrophic Lateral Sclerosis (ALS)

    • The institute researches new treatments for amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig's disease, which affects 350,000 people worldwide. ALS is is a progressive disease with no cure or effective treatment, which attacks motor neurons in the brain and spinal cord, causing muscles to waste away. Patients live an average of two-to-five years after diagnosis.

    Therapy

    • There is currently little therapy and no cure for ALS.
      There is currently little therapy and no cure for ALS.

      Currently there is only a single therapy approved for treating ALS progression, the drug Rilutek (riluzole). The medical community estimates its benefits as modest---extending patient survival by three months. The institute has discovered a molecule in animals that significantly extended the life of animals with ALS.

    Founding

    • The institute was founded in 1999 by James Allen Heywood, after his brother Stephen was diagnosed with ALS, and is located in Cambridge, Massachusetts.

    The Institute's Work

    • The institute has collaborated with dozens of academic labs and leading biotechs worldwide. The institute's industrial-scale organization allows for the development and testing of dozens of potential therapeutics each year, including those relating to gene therapy, immunology and stem-cell therapy.

    Public Outreach

    • The institute relies on donations to do its work.
      The institute relies on donations to do its work.

      The institute's website hosts a public forum on the disease and its research which allows visitors to ask researchers a question. Some of the funding for the institute comes from the ALS community---nonprofit groups, patients and medical facilities. Fund-raising events are posted on its website. A special section on its website provides fund-raising tools, including event development tools and marketing materials.

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  • Photo Credit Image by Flickr.com, courtesy of Hey Paul Image by Flickr.com, courtesy of Daniel Lobo

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