Summary

Eligibility
for males ages 7-27 (full criteria)
Location
at La Jolla, California and other locations
Dates
study started
completion around

Description

Summary

AOC 1044-CS2 (EXPLORE44-OLE) is an Open-label Study to Evaluate the Pharmacodynamics and Long-Term Safety and Tolerability of AOC 1044 Administered Intravenously to DMD Participants with Mutations Amenable to Exon 44 Skipping.

Official Title

A Phase 2 Open-label Study to Evaluate the Pharmacodynamics and Long-Term Safety and Tolerability of AOC 1044 Administered Intravenously to DMD Participants with Mutations Amenable to Exon 44 Skipping

Details

AOC 1044-CS2 (EXPLORE44-OLE) is an open label, extension study to Part B of AOC 1044-CS1 (EXPLORE44). AOC 1044-CS2 is designed to evaluate the pharmacodynamic effect of AOC 1044 on dystrophin protein production in skeletal muscle as well as the long-term safety, tolerability, pharmacokinetics, and exploratory efficacy of AOC 1044.

All participants who enroll in AOC 1044-CS2 will receive active treatment. The treatment period is 2 years with IV dosing every 6 or 8 weeks.

Once participants have completed active treatment, they will be followed through a 3-month safety follow-up period. The sponsor may extend active treatment beyond 2 years at a future timepoint.

Keywords

DMD, Duchenne Muscular Dystrophy, Duchenne, Exon 44, EXPLORE44, EXPLORE44-OLE, EXPLORE44 OLE, Avidity Biosciences, Avidity, AOC 1044, AOC 1044-CS1, AOC 1044-CS2, AOC, Muscular Dystrophies

Eligibility

You can join if…

Open to males ages 7-27

Rollover Participants:

  • Satisfactorily completed AOC 1044-CS1 (EXPLORE44) as determined by the Investigator and Sponsor
  • No significant tolerability issues with AOC 1044

De novo Participants:

  • Aged 7 to 27 years, inclusive, at the time of informed consent
  • Clinical diagnosis of DMD or clear onset of DMD symptoms at or before the age of 6 years
  • Confirmation of DMD gene mutation amenable to exon 44 skipping
  • Weight ≥ 23 kg
  • Ambulatory or non-ambulatory
    • Ambulatory participants: LVEF ≥50% and FVC≥50%
    • Non-ambulatory participants: LVEF ≥45% and FVC≥40%
  • PUL 2.0 entry item A ≥3
  • If on corticosteroids, stable dose for 30 days before screening and throughout the study

You CAN'T join if...

Rollover Participants:

  • Presence of any new condition or worsening of existing condition that could affect a participant's safety or ability to comply with study procedures

De novo Participants:

  • Serum hemoglobin < lower limit of normal
  • Uncontrolled hypertension or diabetes
  • Prior treatment with any cell or gene therapy
  • Prior treatment with another exon 44 skipping agent within 6 months prior to informed consent
  • Recently treated with an investigational drug
  • History of multiple drug allergies

Locations

  • University of California, San Diego, Rady&#39;s Children&#39;s Hospital accepting new patients
    La Jolla California 92037 United States
  • Lucille Packard Children&amp;#39;s Hospital at Stanford accepting new patients
    San Carlos California 94070 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Avidity Biosciences, Inc.
ID
NCT06244082
Phase
Phase 2 research study
Study Type
Interventional
Participants
Expecting 35 study participants
Last Updated