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Families of Spinal Muscular Atrophy Receives FDA Orphan Drug Designation For Quinazoline495 For The Treatment of Spinal Muscular Atrophy
Date:8/28/2009

d our Chapters.

Families of SMA funds and directs the leading SMA research programs. The successful results and progress from basic research to drug discovery programs to clinical trials provides real hope for families and patients:

  • Families of SMA has funded 5 multi-center clinical trials for existing drugs that have potential for SMA.
  • FSMA has directed and funded the leading new drug development program for a therapy specially designed to treat SMA.
  • Families of SMA is building a pipeline of drug discovery programs based on our investments in basic research.
  • FSMA has invested significant resources into alternative approaches that show promise to cure SMA.
  • In 2009 FSMA had over 900 Attendees at the Annual SMA Family and Professionals Conference.

Families of SMA is a non-profit, 501(c)3 tax exempt organization with 26 Chapters throughout the United States and over 65,000 members and supporters.

Web site: http://www.curesma.org


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SOURCE Families of Spinal Muscular Atrophy
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