MDA 2024 poster: Ataluren delays clinically meaningful milestones of decline in 6MWD in patients with nmDMD from Study 041, a phase 3, placebo-controlled trial
This poster, presented at MDA 2024, explores the use of ataluren to prevent ambulatory decline in patients with nonsense mutation Duchenne muscular dystrophy (nmDMD)
Review disease progression milestones and ambulatory decline in nmDMD
Assess the effects of ataluren on the 6-minute walk distance in patients with nmDMD
▼ Ataluren is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system. Adverse events should also be reported to PTC at pharmacovigilance@ptcbio.com.
Registration conditions differ internationally, and prescribing information may vary depending on local approval in each country. The European Summary of Product Characteristics for ataluren is available here. Please refer to your local country guidance for more information.
This poster was developed and funded by PTC Therapeutics for MDA 2024.
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MED-ALL-DMD-2400003 | March 2024
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