ANN ARBOR, Mich., Sept. 15 /PRNewswire/ -- Assay Designs and the Spinal Muscular Atrophy Foundation (SMAF) are very pleased to announce a collaborative agreement for development of reagents and assays for SMN (Survival Motor Neuron) protein to expedite drug discovery and development efforts for spinal muscular atrophy (SMA), the leading genetic cause of mortality in infants and toddlers. "Assay Designs is excited and proud to have been selected by the SMA Foundation, and to help enable better understanding and ultimately improved treatment for this debilitating illness," commented Dan Calvo, President and CEO of Assay Designs. Providing a reliable and widely-available ELISA kit for measuring SMN protein levels will greatly simplify and accelerate the process of assessing the efficacy of potential drugs in clinical trials, which is key to the successful development of new therapeutics for this devastating disease. "We are pleased to bring results from the research sector out for general use in the community," states Loren Eng, president of the SMA Foundation.
SMA is a genetic, motor neuron disease characterized by the wasting of skeletal muscles. Caused by progressive degeneration of nerve cells in the spinal cord, the disease leads to increasing muscular weakness and atrophy. It is estimated that approximately 1 in 6,000 to 1 in 10,000 infants are born annually worldwide with SMA. SMA is often compared to polio because the same spinal cord cells are attacked in each disease. Over time, patients afflicted by this disease continue to lose muscle control and strength, progressively leading to inability to walk, stand, sit up and breathe.
Founded in 2003, the Spinal Muscular Atrophy Foundation is a nonprofit
organization dedicated to accelerating progress towards a treatment and
cure for spinal muscular atrophy through targeted funding of clinical
research and novel drug development efforts. Since its inception, the
Foundation has awarded over $50 m
|SOURCE Assay Designs, Inc.|
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