Study of AOC 1044 in Healthy Adult Volunteers and Participants with Duchenne Muscular Dystrophy (DMD) Mutations Amenable to Exon 44 Skipping

Last updated: March 7, 2025
Sponsor: Avidity Biosciences, Inc.
Overall Status: Completed

Phase

1/2

Condition

Muscular Dystrophy

Treatment

AOC 1044

Placebo

Clinical Study ID

NCT05670730
AOC 1044-CS1
  • Ages 7-55
  • Male
  • Accepts Healthy Volunteers

Study Summary

AOC 1044-CS1 (EXPLORE44) is a Phase 1/2 study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic effects of single and multiple ascending doses of AOC 1044 in healthy adult volunteers and participants with DMD mutations amenable to exon 44 skipping.

Part A is a single dose design with multiple cohorts (dose levels) in healthy adult volunteers.

Part B is a multiple-ascending dose design with 3 cohorts (dose levels) in participants with Duchenne.

Eligibility Criteria

Inclusion

Part A:

Key Inclusion Criteria:

  • Aged 18 to 55 years, inclusive, at the time of informed consent

  • Body mass index (BMI) of 18.5 to 32.0 kg/m2

Exclusion

Key Exclusion Criteria:

  • Clinically significant abnormalities in laboratory results, ECGs, or vitals

  • Current or recent use of prescription or nonprescription drugs

  • Positive drug/alcohol test at Screening or Day -1

  • Elevated blood pressure (BP) >130/80 mmHg at Screening

  • Participation in a clinical study in which an investigational product was receivedwithin 1 month of screening or 5 half-lives of the investigational product

  • Blood or plasma donation within 16 weeks of planned AOC 1044 administration Note:Other protocol defined Inclusion/Exclusion criteria may apply

Part B:

Key Inclusion Criteria:

  • 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 6years

  • 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 thestudy

Key Exclusion Criteria:

  • Biceps brachii muscles unsuitable for biopsy

  • 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 toinformed consent

  • Recently treated with an investigational drug

  • History of multiple drug allergies

Study Design

Total Participants: 70
Treatment Group(s): 2
Primary Treatment: AOC 1044
Phase: 1/2
Study Start date:
November 09, 2022
Estimated Completion Date:
November 25, 2024

Connect with a study center

  • Arkansas Children's

    Little Rock, Arkansas 72202
    United States

    Site Not Available

  • UCSD

    La Jolla, California 92037
    United States

    Site Not Available

  • Stanford University

    Palo Alto, California 94304
    United States

    Site Not Available

  • Rare Disease Research - Atlanta

    Atlanta, Georgia 30329
    United States

    Site Not Available

  • University of Iowa

    Iowa City, Iowa 52242
    United States

    Site Not Available

  • University of Massachusetts Chan Medical School

    Worcester, Massachusetts 01655
    United States

    Site Not Available

  • Gillette Children's

    Saint Paul, Minnesota 55101
    United States

    Site Not Available

  • Gillette Children's

    St. Paul, Minnesota 55101
    United States

    Site Not Available

  • Rare Disease Research NC

    Hillsborough, North Carolina 27278
    United States

    Site Not Available

  • Abigail Research Institute at Nationwide Children's Hospital

    Columbus, Ohio 43215
    United States

    Site Not Available

  • Worldwide Clinical Trials (Part A only)

    San Antonio, Texas 78217
    United States

    Site Not Available

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