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AVAILABLE
NCT07250737

Managed Access Program for Del-zota in Participants With DMD Mutations Amenable to Exon 44 Skipping

Sponsor: Avidity Biosciences, Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

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