Phase 1/2 Study of AOC 1020 in Adults With Facioscapulohumeral Muscular Dystrophy (FSHD)
a study on Facioscapulohumeral Muscular Dystrophy FSHD1 FSHD2 FMD FMD2 Fascioscapulohumeral Muscular Dystrophy Fascioscapulohumeral Muscular Dystrophy Type 1 Dystrophies, Facioscapulohumeral Muscular Facio-Scapulo-Humeral Dystrophy Atrophy, Facioscapulohumeral Atrophies, Facioscapulohumeral Facioscapulohumeral Atrophy Muscular Dystrophies FSH Muscular Dystrophy Landouzy Dejerine Dystrophy Landouzy-Dejerine Muscular Dystrophy Dystrophies, Landouzy-Dejerine Dystrophy, Landouzy-Dejerine Landouzy-Dejerine Syndrome Muscular Dystrophy, Landouzy Dejerine Progressive Muscular Dystrophy FSH
Summary
- Eligibility
- for people ages 18-65 (full criteria)
- Location
- at San Diego, California and other locations
- Dates
- study startedestimated completion
Description
Summary
A Randomized, Double-blind, Placebo-controlled, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Exploratory Efficacy of AOC 1020 Administered Intravenously to Adult Participants with Facioscapulohumeral Muscular Dystrophy (FSHD)
Official Title
A Randomized, Double-blind, Placebo-controlled, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Exploratory Efficacy of AOC 1020 Administered Intravenously to Adult Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)
Details
AOC 1020-CS1 is a first-in-human, 3-part, multi-center, Phase 1/2, randomized, double-blind, placebo-controlled study designed to evaluate safety, tolerability, pharmacokinetics and to explore pharmacodynamics and efficacy of single and multiple-doses of AOC 1020 administered intravenously in adult participants with FSHD Type 1 (FSHD1) and FSHD Type 2 (FSHD2).
Part A is a dose titration design which includes a single and multiple dose schedule with 1 cohort. Part B is a single-ascending and multiple-ascending dose design with 2 cohorts. Part C is a parallel, multi-dose cohort design with 1 cohort. For each of Part A, B, and C the patient duration is 12 months as the active treatment period is approximately 9 months followed by a 3-month follow-up period. Once participants have completed active treatment and the follow-up period, they may have the option to participate in a planned open-label extension. If patients do not enroll in the open-label extension, they will be followed through a 6-month safety follow-up period.
Keywords
FSHD, FSHD1, FSHD2, FMD, FMD2, Fascioscapulohumeral Muscular Dystrophy, Fascioscapulohumeral Muscular Dystrophy Type 1, Fascioscapulohumeral Muscular Dystrophy Type 2, Dystrophies, Facioscapulohumeral Muscular, Dystrophy, Facioscapulohumeral Muscular, Facioscapulohumeral Muscular Dystrophy 1, Facioscapulohumeral Muscular Dystrophy 2, Facio-Scapulo-Humeral Dystrophy, Atrophy, Facioscapulohumeral, Atrophies, Facioscapulohumeral, Facioscapulohumeral Atrophy, Muscular Dystrophies, Muscular Dystrophy, Facioscapulohumeral, FSH Muscular Dystrophy, Landouzy Dejerine Dystrophy, Landouzy-Dejerine Muscular Dystrophy, Dystrophies, Landouzy-Dejerine, Dystrophy, Landouzy-Dejerine, Landouzy-Dejerine Syndrome, Muscular Dystrophy, Landouzy Dejerine, Progressive Muscular Dystrophy, FSH, FORTITUDE, Avidity, Avidity Biosciences, AOC 1020, Facioscapulohumeral Muscular Dystrophy, Atrophy
Eligibility
You can join if…
Open to people ages 18-65
- FSHD1 or FSHD2 diagnosis confirmed by documented genetic testing (testing provided by Sponsor)
- Ambulatory and able to walk 10 meters (with or without assistive devices such as one cane, walking stick or braces)
- At least 1 muscle region suitable for biopsy (testing provided by Sponsor)
- Muscle weakness in both upper and lower body, as determined by Investigator
You CAN'T join if...
- Diagnosed with congenital or infantile FSHD
- Pregnancy, intent to become pregnant within 9 months after last planned dose of Study Drug, or active breastfeeding
- Unwilling or unable to continue to comply with contraceptive requirements
- Body mass index (BMI) >35.0 kg/m2 at Screening
- History of muscle biopsy within 30 days of the screening biopsy or planning to undergo any nonstudy muscle biopsies over the duration of the study
- History of bleeding disorders, significant keloid, or other skin or muscle conditions (e.g., severe muscle wasting) that, in the opinion of the Investigator, makes the participant unsuitable for serial muscle biopsy
- Anticipated survival less than 2 years
- Blood or plasma donation within 16 weeks of Study Day 1
- Any contraindication to MRI
- Any abnormal lab values, conditions or diseases that, in the opinion of the investigator or Sponsor, would make the participant unsuitable for the study or could interfere with participation or completion of the study
- Treatment with any investigative medication within 1 month (or 5 half-lives of the drug, whichever is longer) of Screening
Locations
- University of California San Diego
not yet accepting patients
San Diego California 92093 United States - University of California, Irvine
not yet accepting patients
Irvine California 92697 United States
Details
- Status
- accepting new patients at some sites,
but this study is not currently recruiting here - Start Date
- Completion Date
- (estimated)
- Sponsor
- Avidity Biosciences, Inc.
- Links
- Related Info
- ID
- NCT05747924
- Phase
- Phase 1/2 research study
- Study Type
- Interventional
- Participants
- Expecting 72 study participants
- Last Updated