Open
Actively Recruiting
Study of ATX-01 in Participants With DM1
About
Brief Summary
The goal of this clinical trial is to test ATX-01 in participants with myotonic dystrophy type 1 (DM1). The main question it aims to answer is if ATX-01 is safe and well tolerated. The trial will compare the safety and tolerability of ATX-01 and a matching placebo.
There will be a single-ascending dose part of the trial and a multiple-ascending dose part. In the single-ascending dose, participants will receive one dose of ATX-01 or placebo. In the multiple-ascending dose part, participants will receive three doses of ATX-01 or placebo.
ATX-01 is a novel anti-miR (synthetic single stranded oligonucleotide) that inhibits a microRNA called miR-23b.
Primary Purpose
Study Type
Phase
Eligibility
Gender
Healthy Volunteers
Minimum Age
Maximum Age
Key Inclusion Criteria:
- Participants with a documented clinical diagnosis of DM1 (CTG expansion of >150 repeats in DMPK gene measured in peripheral blood mononuclear cells)
- Ambulatory, defined as able to complete a 10-meter walk/run test at screening without the use of assistive devices such as canes, walkers, or orthoses, except for ankle-foot orthoses
- Presence for >3 seconds of grip myotonia as confirmed by a central reader
Key Exclusion Criteria:
- Participants with congenital DM1
- Medical Research Council Muscle Scale score of less than 4 on ankle dorsiflexion or significant tibialis anterior atrophy that prevents a muscle biopsy
- Use of mexiletine or other agent for myotonia within 21 days or 5 half-lives, whichever is longer, prior to screening
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Study Stats
Protocol No.
25-0987
Category
Genetic and Rare Diseases
Musculoskeletal Disorders
Principal Investigator
Contact
Location
- UCLA Westwood