More than 800 Advocates, Pharmaceutical Companies, Regulators, Scientific & Medical Leaders Convene to Discuss Pressing Issues Facing 30 Million Americans with a Rare Disease
National Organization for Rare Disorders Hosts 2023 Breakthrough Summit To Discuss Most Pressing Issues Facing 30 Million Americans with a Rare Disease. More Than 800 Advocates, Pharmaceutical Companies, Regulators, Scientific & Medical Leaders Convene To Improve Rare Disease Patient Care and Accelerate Drug Development for More than 7,000 Known Rare Diseases - - Of Which 95% Are Without an FDA-Approved Treatment.
WHAT:
Join the National Organization for Rare Disorders (NORD) Oct. 15-17, 2023 in Washington for the Rare Diseases and Orphan Products Breakthrough Summit. This event brings together rare disease advocates, experts, and stakeholders in the United States and around the world to tackle the most pressing issues facing America's rare disease community.
The two-day event will focus on critical topics faced in diagnosing and finding treatments for more than 7,000 rare diseases that impact 1 in 10 Americans. Topics range from; the impact of the Inflation Reduction Act, thenew frontier of gene editing, harnessing the power of AI, equitable access to care, mental health needs and more.
WHO:
-Peter Saltonstall, President and Chief Executive Officer, NORD
-Robert Califf, MD, Commissioner, U.S. Food and Drug Administration
Special CEO Perspectives Panel:Outlook for Rare Diseases and Orphan Products
-R. Duane Clark, General Manager, U.S. Rare Diseases, Sanofi
-Eric Dube, Ph.D., President and Chief Executive Officer, Travere
-Myrtle Potter, President and Chief Executive Officer, Sumitomo Pharma America
-Brigette Roberts, M.D., OrphAI Therapeutics
-Stephen Uden, M.D., Co-Founder and Chief Executive Officer, Rallybio
WHEN/WHERE:
Oct. 16-17, 2023, Marriot Marquis, Washington
Livestream is available upon request
WHY:
Rare disease is a public health challenge. From small towns to large cities, more than 30 million Americans have a rare disease. Half are children, of which one in three will die before their fifth birthday. Diagnosis can take five years or more and overall medical costs are three to five times higher than non-rare diseases. Patients with rare disease incur nearly half of all healthcare costs in the U.S. (Sources: https://ncats.nih.gov/files/NCATS_RareDiseasesFactSheet.pdf, https://genomemedicine.biomedcentral.com/articles/10.1186/s13073-022-01026-w).
SOURCE National Organization for Rare Disorders (NORD)
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