Confirmed Supporters
Confirmed Supporters
We would like to thank the following companies for their support.
EXHIBITORS
Amicus Therapeutics
ATOM International
ATOM International provides functional testing training and oversight in the support of rare neuromuscular disorders. Our global team of physiotherapists help ensure consistency and confidence in study data via standardized training and comprehensive oversight and documentation.
atom-international.org
atom-international.org
argenx
argenx is a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Partnering with patients, healthcare professionals, and leading academic researchers, argenx aims to translate immunology breakthroughs into a world-class portfolio of accessible novel antibody-based medicines for patients living with chronic immune-mediated diseases.
argenx.com
argenx.com
DEYMED Diagnostic
DEYMED Diagnostic is a leading Czech company with an established global existence, specialising in advanced medical diagnostic and treatment technologies for neurophysiology and psychiatry. Founded in 1997, DEYMED has expanded its product range over the years to include EEG, EMG, TMS (Transcranial Magnetic Stimulation), PSG (Polysomnography), and BFB (Biofeedback) systems, trusted by healthcare providers worldwide for their precision, reliability, and ease of use.
deymed.com
deymed.com
European Neuromuscular Centre (ENMC)
Dyne Therapeutics
Dyne Therapeutics is focused on discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE™ platform, Dyne is developing targeted therapeutics that are designed to overcome limitations in delivery to muscle tissue and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.
dyne-tx.com
dyne-tx.com
Italfarmaco
Italfarmaco is a global pharmaceutical company operating in over 90 countries and committed to improving patients’ lives through pioneering solutions in women’s health, neurology, cardiovascular, and rare conditions. Its rare disease unit is advancing therapies for Duchenne muscular dystrophy and amyotrophic lateral sclerosis, while also developing candidates for Becker muscular dystrophy and polycythemia vera. (EU-ITFRD-25-00006)
italfarmaco.com/therapeutic-areas/rare-diseases
italfarmaco.com/therapeutic-areas/rare-diseases
Johnson & Johnson
LFB BIOMEDICAMENTS
LFB is a French biopharmaceutical group that develops, manufactures and markets plasma-derived medicinal products and recombinant proteins for the treatment of patients with serious and often rare diseases, in immunology, haemostasis, and intensive care. Created in 1994, LFB today is a leading European company providing plasma-derived medicines to healthcare professionals.
groupe-lfb.com
groupe-lfb.com
Lupin Neurosciences
Merck
MGBase Registry
The MGBase Registry, supported by the MSBase Foundation, is a global collaborative registry for clinicians in Myasthenia Gravis (MG). It enables collection, tracking and evaluation of patient outcomes through free, secure, web-based tools accessible anywhere on any device, offering scientific support to advance research and improve understanding of MG worldwide.
mgbase.org
mgbase.org
Santhera
Santhera Pharmaceutical is a Swiss commercial stage biopharmaceutical company committed to developing and commercializing innovative medicines for patients living with rare and other diseases with high unmet medical needs. We are focusing on the development of treatments for neuromuscular diseases that currently lack treatment options, such as Duchenne muscular dystrophy (DMD).
santhera.com
santhera.com
Sarepta
Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases.
sarepta.com
sarepta.com
Scholar Rock
Scholar Rock is a late-stage biopharmaceutical company on a mission to discover, develop, and deliver life-changing therapies for serious diseases with high unmet need. As a global leader in transforming growth factor beta (TGFβ) superfamily biology, the company is focused on advancing innovative treatments where protein growth factors are fundamental.
scholarrock.com
scholarrock.com
UCB Biopharma
UCB Biopharma aims to improve lives by addressing disease challenges through innovative research in neurology, immunology, and more. Guided by patient perspectives, UCB delivers meaningful solutions globally, fostering collaboration, diversity, and care for people, communities, and the planet, from its Belgian headquarters to nearly 40 countries.
ucb.com
ucb.com
University of Rochester Center for Health and Technology (CHeT)
Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases.University of Rochester Center for Health and Technology (CHeT) Outcomes team develops and validates highly sensitive, disease-specific, regulatory-grade patient and caregiver reported outcome measures for therapeutic trials and drug labelling claims. Our Health Indexes span 40+ neurological, neuromuscular, and movement disorders and have been used worldwide in over 40 languages.
urmc.rochester.edu/chet/our-expertise/outcomes
urmc.rochester.edu/chet/our-expertise/outcomes
Vor Biopharma
Vor Bio is a clinical-stage biotechnology company rapidly advancing telitacicept, designed to modulate the immune system and deliver meaningful treatment for people living with autoimmune disease. By targeting the BAFF/APRIL pathway, Vor Bio aims to address disease at its source in serious B-cell driven conditions to improve patients’ daily lives.
vorbio.com
vorbio.com