John F. Crowley, President and CEO of the Biotechnology Innovation Organization (BIO), to Deliver Keynote Address on the Future of Biotech and Rare Disease Innovation at the 2026 MDA Clinical & Scientific Conference

New York, Dec. 08, 2025 (GLOBE NEWSWIRE) -- The Muscular Dystrophy Association (MDA) announced today that John F. Crowley, President and CEO of the Biotechnology Innovation Organization (BIO), will deliver the keynote address at the 2026 MDA Clinical & Scientific Conference, taking place March 8โ€“11, 2026, in Orlando, Florida. The annual MDA Clinical & Scientific Conference is the largest global neuromuscular meeting dedicated to uniting thousands of scientific researchers, clinicians, affiliated healthcare providers, industry leaders, and patient advocates in pursuit of innovation for the next 75 years of MDAโ€™s mission serving the neuromuscular community. Crowleyโ€™s keynote presentation will take place on Monday, March 9 at 9:30am ET, both in person and via live stream. Registration for in-person and virtual attendance is available at MDAConference.org.

John F. Crowley, President and CEO of the Biotechnology Innovation Organization (BIO) said, โ€œWe are living in an extraordinary era for biotechnologyโ€”one where innovation, data-driven insights, and patient partnerships are transforming whatโ€™s possible for people living with rare diseases. For 75 years, the Muscular Dystrophy Association has embodied that spirit, fueling discovery, accelerating new therapies, and uniting a global community of scientists, clinicians, affiliated healthcare providers, advocates, and families. I am honored to be part of this important conference and look forward to a lively gathering that deepens relationships, moves science forward and builds the types of partnerships that will transform the standard of care for patients around the world."

Driving the Future of Innovation, Policy, and Patient Impact
Crowleyโ€™s keynote, โ€œDriving the Future of Innovation, Policy, and Patient Impact,โ€ will explore how patient-driven advocacy, biotechnology entrepreneurship, and emerging technologies are transforming the landscape of medical research and care. He will highlight the vital role of organizations like Muscular Dystrophy Association and BIO in building a robust ecosystem that empowers early diagnosis, fosters equitable access, and accelerates the development of transformative therapies for rare and neuromuscular diseases.

โ€œJohn Crowleyโ€™s extraordinary journey, from father and entrepreneur to global leader in biotechnology, perfectly reflects the Muscular Dystrophy Associationโ€™s enduring mission,โ€ said Sharon Hesterlee, PhD, Interim President and CEO, MDA. โ€œHis laser focused dedication to scientific innovation and patient advocacy has driven tangible change for families around the world. His keynote will inspire our community to continue pushing the boundaries of whatโ€™s possible in research, care, and access.โ€

About John F. Crowley
A biotechnology pioneer and passionate champion for the rare disease community, John Crowley serves as President and CEO of the Biotechnology Innovation Organization (BIO), representing biotech companies and industry leaders around the world. His journey began as a father determined to save his childrenโ€™s lives after they were diagnosed with Pompe disease, a rare and often fatal neuromuscular disorder. Crowley left his corporate career to co-found Novazyme Pharmaceuticals, later acquired by Genzyme Corporation, where his leadership helped advance the first treatment for Pompe diseaseโ€”a therapy that has transformed countless lives. He went on to found and lead Amicus Therapeutics, serving as CEO from 2005 to 2022, where he continued his mission to bring hope and new therapies to families affected by rare diseases. His familyโ€™s remarkable story inspired The Cure by Pulitzer Prizeโ€“winning journalist Geeta Anand and the major motion picture Extraordinary Measures, starring Brendan Fraser, Harrison Ford, and Keri Russell.

Social Media Engagementย 
MDA will be sharing updates and information on its social media channels usingย #MDAconference. The social media engagement toolkit is available here.
Follow MDA onย Instagram,ย Facebook,ย X,ย Threads,ย Bluesky,ย TikTok,ย LinkedIn, andย YouTube.

Registrationย 
For additional information and to register, clickย here. Early bird registration deadline is December 31, 2025.ย 

Sponsorsย 
MDA extends its appreciation to the premier sponsors whose support helps bring the neuromuscular community together at the 2026 MDA Clinical & Scientific Conference, including: Strength of Life: argenx, Biogen, BridgeBio, Novartisย 
Circle of Strength: ITF Therapeutics, Scholar Rockย 

Media inquiries emailย press@mdausa.org.ย 

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About the MDA Clinical & Scientific Conferenceย 
MDA is the convener of the largest global gathering of the neuromuscular disease community. The four-day international event will bring together renowned researchers, clinicians, affiliated health care providers, academicians, advocates, and industry leaders to explore the latest advances in the field of neuromuscular disease. Last yearโ€™s MDA Clinical & Scientific Conference included over 2,500 attendees (2,000 in-person; 500 virtual) from 41 countries with 8 specialized tracks, 39 sessions, 207 speakers, 56 exhibitors, 18 industry sponsored forums, 236 in-person posters, 379 virtual posters, 56 oral poster presentations, and 20 patient advocacy organizations exhibiting (with 37 organizations participating in the NMAC meeting). This conference is the largest worldwide gathering of the neuromuscular disease community and serves as a vital platform for knowledge-sharing and collaboration.ย 

About Muscular Dystrophy Associationย 
Muscular Dystrophy Associationย (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and over 300 other neuromuscular conditions. For 75 years, MDA has led the way in accelerating research, advancing care, and advocating support and inclusion of families living with neuromuscular disease. MDA's mission is to empower the people we serve to live longer, more independent lives. To learn more visitย mda.orgย and follow MDA onย Instagram,ย Facebook,ย X,ย Threads,ย Bluesky,ย TikTok,ย LinkedIn, andย YouTube.ย 

About Muscular Dystrophy Associationโ€™s 75thย Anniversaryย 
In 2025, the Muscular Dystrophy Association proudly marks 75 years of legacy, impact, and momentum in the fight against neuromuscular diseases. Since our founding, MDA has been at the forefront of research breakthroughs, providing access to comprehensive care, and championing the rights of people living with muscular dystrophy, ALS, and over 300 other neuromuscular diseases. This milestone has been made possible by generations of dedicated support from people living with neuromuscular disease, their families, researchers, clinicians, volunteers, and donorsโ€”who boldly drive our mission forward. As we look ahead, we remain committed to honoring thisย legacy, building on theย impactย weโ€™ve made together, and continuing ourย momentumย toward transformative progress for people living with neuromuscular disorders. Learn more atย MDA75.org.

Attachments


Mary Fiance, National Vice President, Strategic Communications
Muscular Dystrophy Association
press@mdausa.org

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