Clinical Research Directory
Browse clinical research sites, groups, and studies.
Managed Access Program for Del-zota in Participants With DMD Mutations Amenable to Exon 44 Skipping
Sponsor: Avidity Biosciences, Inc.
Summary
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.
Official title: Managed Access to Investigational Use of AOC 1044 in Participants With DMD Mutations Amenable to Exon 44 Skipping
Key Details
Gender
MALE
Age Range
6 Years - Any
Study Type
EXPANDED_ACCESS
Enrollment
Not specified
Start Date
Not specified
Completion Date
Not specified
Last Updated
2026-04-27
Healthy Volunteers
Not specified
Conditions
Interventions
delpacibart zotadirsen
Del-zota is administered as an IV infusion every 6 weeks. Doses are administered based on body weight.
Locations (6)
Arkansas Children's Hospital
Little Rock, Arkansas, United States
Rare Disease Research
Atlanta, Georgia, United States
UMass Memorial Health Care
Worcester, Massachusetts, United States
Gillette Children's
Saint Paul, Minnesota, United States
Prisma Health-Midlands Children's Hospital
Columbia, South Carolina, United States
University of Vermont Medical Center
Burlington, Vermont, United States