WMS 2023 poster presentation: Updated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE Registry
This poster presentation, given as part of WMS 2023, explores the safety data of ataluren in patients with nonsense mutation Duchenne muscular dystrophy and a variety of characteristics
Explore the patient demographics for patients in the STRIDE Registry
Compare treatment emergent adverse events when receiving ataluren with or without corticosteroids
Understand the updated safety data of ataluren through this long-term, real-world analysis
▼ 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 presentation was developed and funded by PTC Therapeutics for WMS 2023.
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