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Newswise PHILADELPHIA Three longtime allies have joined forces to create the new Penn Medicine\/CHOP Friedreichs Ataxia Center of Excellence. The establishment of the center was catalyzed by a $3.25 million gift from the Friedreichs Ataxia Research Alliance (FARA), in partnership with the Hamilton and Finneran families. <\/p>\n
For the past 16 years Penn Medicine, The Childrens Hospital of Philadelphia (CHOP), and FARA, a nonprofit organization dedicated to curing FA, have collaborated to provide and push forward the care needed by FA patients. <\/p>\n
Friedreichs ataxia (FA) is a rare, progressive neurogenetic condition found in approximately 1 in 50,000 people worldwide. While it is relatively rare, it is the most common form of inherited ataxia, a condition characterized by progressive lack of coordinated movement and loss of balance. FA also involves degeneration of heart muscle and nerve cells. Onset of symptoms usually occurs in childhood, and most patients are confined to a wheelchair by their mid-to-late twenties. Myocardial failure and\/or arrhythmias are the most common cause of premature death. Currently there are no approved drugs to treat FA. <\/p>\n
FARA, CHOP, and Penn Medicine have also shared in research and clinical trials that have elucidated the metabolic dysfunction underlying FA. Their work has created a database of well-documented patients and a pipeline of more than 20 drug candidates ready to be mined for new therapies. Today the FA clinical program at CHOP is the largest in the world. <\/p>\n
Nothing is more rewarding than seeing science at work in the service of the patients and families who suffer from rare diseases such as Friedreichs ataxia, says Glen N. Gaulton, PhD, executive vice dean and chief scientific officer at the Perelman School of Medicine at the University of Pennsylvania. Penn and CHOP are fortunate to support many faculty who dedicate their careers to the care of patients with and research on such rare diseases as FA. Funding for rare disease research is a constant challenge. We are thankful to the donors for this generous gift that significantly enhances our ability to make progress toward new biomarkers, drugs and hopefully, in time, therapies for FA. <\/p>\n
The new Centers team is working with pharmaceutical industry partners to develop drug candidates as well as biomarkers for FA, and this effort fits alongside a broader initiative at Penn Medicine: a gift from an anonymous donor recently founded the Center for Orphan Disease Research and Therapy to support the pursuit of novel therapies for rare diseases of all kinds. <\/p>\n
Integrating cardiac expertise into the care of patients is one major step forward this gift allows us to pursue, says Philip R. Johnson, MD, executive vice president and chief scientific officer at CHOP. Rare diseases are often an area where philanthropy can make a difference, and the generosity of these donors will make a significant impact. <\/p>\n
The Friedreichs Ataxia Center of Excellence is co-directed by David Lynch, MD, PhD, FA program director at CHOP, and Robert B. Wilson, MD, PhD, professor of Pathology and Laboratory Medicine at the Perelman School of Medicine. Lynch and Wilson both serve on FARAs Scientific Advisory Board, and Wilson was a founding member of FARAs board of directors and first chairman of its Scientific Review Committee. Wilson has completed a high-throughput drug screen of more than 340,000 compounds for FA drug discovery and is now working with medicinal chemists to narrow in on candidates for clinical trials. <\/p>\n
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$3.25 Million Gift Creates Penn Medicine\/CHOP Friedreich's Ataxia Center of Excellence<\/a><\/p>\n","protected":false},"excerpt":{"rendered":" Contact Information Available for logged-in reporters only Newswise PHILADELPHIA Three longtime allies have joined forces to create the new Penn Medicine\/CHOP Friedreichs Ataxia Center of Excellence. The establishment of the center was catalyzed by a $3.25 million gift from the Friedreichs Ataxia Research Alliance (FARA), in partnership with the Hamilton and Finneran families. Continue reading