NEW YORK, Feb. 9, 2022 /PRNewswire/ — The Muscular Dystrophy Association (MDA) announced today the schedule for the 2022 MDA Clinical & Scientific Conference. After two years of pivoting to an innovative virtual event, the organization is convening renowned researchers, clinicians, academicians, advocates, and industry leaders from around the world both in person at the Gaylord Opryland Resort and Convention Center in Nashville, Tennessee, March 13-16, 2022, and via live stream. More than 1,200 neuromuscular clinicians and researchers from the United States and around the world, are expected to gather to hear from more than 120 renowned expert presenters in 29 sessions on the latest clinical care and research advances for more than 40 neuromuscular diseases such as Duchenne muscular dystrophy (DMD), amyotrophic lateral sclerosis (ALS), Charcot-Marie-Tooth (CMT), and spinal muscular atrophy (SMA).
This year’s conference also features 200 abstracts that will take the form of posters or talks that will highlight basic, translational, and clinical research. Day four of the conference will be devoted to oral presentations from selected abstracts submitted by scientific and clinical researchers. In addition, MDA will host the 2nd Annual Insights in Research Investor Summit (IRIS), which will provide an opportunity for companies and inventors in the neuromuscular disease space to showcase investment and licensing opportunities. Outside of the sessions, the Patient Advocacy Pavilion will provide an engaging environment for advocates and industry partners to collaborate in meaningful ways. The full conference agenda is available here.
“MDA’s annual conference is the largest and most important convening on advances in understanding and treating neuromuscular diseases in the world. We bring together scientists and clinicians from around the globe to share their progress, best practices for conducting research, new diagnostic approaches, and information on treatments. As a researcher myself earlier in my career, I am both proud and excited to welcome the attendees of this conference, both in-person and remote, and get the chance to hear about the groundbreaking work they are doing in the field of neuromuscular disease research,” said Donald S. Wood, PhD, president and CEO of MDA.
“The MDA Clinical & Scientific Conference has become a prime destination for academic researchers, pharmaceutical and biotech companies to report on their latest clinical trial findings,” said MDA’s Chief Research Officer, Sharon Hesterlee. “Our conference is the only one in the neuromuscular space that really combines everything from basic research to clinical care, treatment, and management.”
MDA anticipates several high-profile data presentations on Wednesday, March 16, during clinical trial presentations. Among the session highlights are:
About the Muscular Dystrophy Association
For 70 years, the Muscular Dystrophy Association (MDA) has been committed to transforming the lives of people living with muscular dystrophy, ALS, and related neuromuscular diseases. We do this through innovations in science and innovations in care. As the largest source of funding for neuromuscular disease research outside of the federal government, MDA has committed more than $1 billion since our inception to accelerate the discovery of therapies and cures. Research we have supported is directly linked to life-changing therapies across multiple neuromuscular diseases. MDA’s MOVR is the first and only data hub that aggregates clinical, genetic, and patient-reported data for multiple neuromuscular diseases to improve health outcomes and accelerate drug development. MDA supports the largest network of multidisciplinary clinics providing best-in-class care at more than 150 of the nation’s top medical institutions. Our Resource Center serves the community with one-on-one specialized support, and we offer educational conferences, events, and materials for families and healthcare providers. MDA Advocacy supports equal access for our community, and each year thousands of children and young adults learn vital life skills and gain independence at summer camp and through recreational programs, at no cost to families. During the COVID-19 pandemic, MDA continues to produce virtual events and programming to support our community when in-person events and activities are not possible. MDA’s COVID-19 guidelines and virtual events are posted at mda.org/COVID19. For more information, visit mda.org.
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SOURCE Muscular Dystrophy Association
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