The purpose of this study is to evaluate the safety, tolerability, and efficacy of LE051 intravenous therapy in DMD patients treated with exon 51 skipping therapy.
This is a single-arm, open-label study to evaluate the safety, tolerability, efficacy, pharmacokinetic, pharmacodynamic, and immune response of LE051 after a single intravenous infusion in DMD patients, as well as the long-term safety and efficacy. Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disorder arising from mutations in the dystrophin gene, leading to muscle weakness, disability, and premature mortality. LE051, an investigational therapy, incorporates a ADAR recruiting RNA expression cassette targeting human exon 51 and is delivered via adeno-associated virus. By inducing exon 51 skipping, LE051 holds the potential to treat approximately 13% of DMD patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
LE051 dose escalation : dose 1 and dose 2.
Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai Municipality, China
RECRUITINGFrequency of AEs, SAEs
Time frame: from day 1 to week 52 after treatment
Changes in North Star Ambulatory Assessment (NSAA) Scores Compared to Baseline
The North Star Ambulatory Assessment (NSAA) comprises 17 items yielding a total score between 0 and 34 points, with increased scores correlating with improved motor performance.
Time frame: from day 1 to week 52 after treatment
Changes in 6-Minute Walk Distance Compared to Baseline
Time frame: from day 1 to week 52 after treatment
Changes in Supine-to-Stand Time Compared to Baseline
Time frame: from day 1 to week 52 after treatment
Changes in 4-Stair Climb Time Compared to Baseline
Time frame: from day 1 to week 52 after treatment
Changes in 10-Meter Walk/Run Time Compared to Baseline
Time frame: from day 1 to week 52 after treatment
Changes in Dystrophin Protein Expression Levels in Muscle Tissue Compared to Baseline
Time frame: from day 1 to week 52 after treatment
Changes in the Percentage of Dystrophin-Positive Muscle Fibers Compared to Baseline
Time frame: from day 1 to week 52 after treatment
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