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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

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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MED-ALL-DMD-2500001 | June 2025

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MED-ALL-CORP-2200029 | June 2025

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