Wave: Encouraging Data From Duchenne Study
- Wave Life Sciences Ltd announced an update from the initial cohort of the Phase 1b/2a proof-of-concept study of WVE-N531 in three boys with Duchenne muscular dystrophy (DMD) amenable to exon 53 skipping.
- High muscle concentrations of WVE-N531 and exon skipping were observed six weeks after initiating biweekly multi-dosing at 10 mg/kg, achieving proof-of-concept in the study.
- WVE-N531 also appeared safe and well-tolerated.
- WVE-N531 resulted in a mean tissue concentration of 42 micrograms/gram (6.1 micromolar).
- Plasma concentrations and other pharmacokinetic parameters following a single dose of 10 mg/kg demonstrated a half-life of 25 days, which may support monthly dosing.
- Adverse events were mild. There were no serious adverse events, no trends in labs, and no oligonucleotide class-related safety events.
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