The purpose of this Managed Access Program is to allow access to delpacibart zotadirsen (AOC 1044) for eligible patients diagnosed with DMD mutations amenable to exon 44 skipping. The patient's Administering Physician should follow the suggested treatment guidelines and comply with all local health authority regulations.
Study Type
EXPANDED_ACCESS
Del-zota is administered as an IV infusion every 6 weeks. Doses are administered based on body weight.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.