A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD
Purpose
A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Intravenous AOC 1020 for the Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD)
Conditions
- Facioscapulohumeral Muscular Dystrophy
- FSHD
- FSHD - Facioscapulohumeral Muscular Dystrophy
- FSHD1
- FSHD2
- Fascioscapulohumeral Muscular Dystrophy
- Fascioscapulohumeral Muscular Dystrophy Type 1
- Fascioscapulohumeral Muscular Dystrophy Type 2
- Facioscapulohumeral Muscular Dystrophy 1
- Facioscapulohumeral Dystrophy
- Facio-Scapulo-Humeral Dystrophy
- Facioscapulohumeral Muscular Dystrophy 2
- Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1)
- FSH Muscular Dystrophy
- Landouzy Dejerine Dystrophy
- Landouzy-Dejerine Muscular Dystrophy
- Landouzy-Dejerine Syndrome
Eligibility
- Eligible Ages
- Between 16 Years and 70 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Clinical and genetic diagnosis of FSHD1 or FSHD2 - Ability to walk independently at pre-specified walking speed (orthoses and ankle braces allowed) for at least 10 meters at screening - Adequate muscle strength based on QMT composite score
Exclusion Criteria
- Breastfeeding, pregnancy, or intent to become pregnant during the study - Unwilling or unable to comply with contraceptive requirements - Abnormal lab values, conditions or diseases that would make the participant unsuitable for the study - Blood Pressure > 140/90 mmHg at Screening - Treatment with another investigational drug or biological agent within 1 month of Screening or 5 half-lives of the drug, whichever is longer - Treatment with an oligonucleotide within 9 months of Screening
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental del-brax |
Del-brax (AOC 1020) will be administered 13 times |
|
|
Placebo Comparator placebo |
Saline will be administered 13 times |
|
Recruiting Locations
Rochester, New York 14642
More Details
- NCT ID
- NCT07038200
- Status
- Recruiting
- Sponsor
- Avidity Biosciences, Inc.
Detailed Description
The study consists of a Screening Period of up to 6 weeks and 72-week Treatment Period. The anticipated duration is approximately 78 weeks. Participants will be randomized to receive an intravenous infusion of either del-brax or placebo at the clinical study site every 6 weeks for a total of 13 doses. The final dose will occur at Week 72, followed by a final assessment at Week 78. After completion of the Week 78 visit, eligible participants will have the option to enroll into an open label extension (OLE) study, pending regulatory approval. Participants who decline participation in the OLE will be followed for a period of 12 weeks for safety. An Independent Data Monitoring Committee (IDMC) comprising members independent and external to the Sponsor will review safety, tolerability, and efficacy (as needed) data of this study at regular intervals.