ICNMD 2024 symposium: Spotlight on nmDMD exploring a targeted treatment option
This symposium, presented at ICNMD 2024, provides an overview of clinical trial and real-world data for nonsense mutation Duchenne muscular dystrophy (nmDMD) and highlights the importance of continuous care
- Understand the developmental timeline of ataluren
- Review clinical and real-world evidence for ataluren in patients with nmDMD
- Appreciate the importance of continuous care through real-world case studies
Registration conditions differ internationally; always consult local prescribing information and/or Summary of Product Characteristics before prescribing any products.
MED-ALL-ATLN-2500006 | September 2025
This symposium was developed and funded by PTC Therapeutics for ICNMD 2024.
The information in the materials was correct at the time of the events.
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