With 48-week data from a Phase II open-label trial in Duchenne muscular dystrophy (DMD) showing an advancement in clinical benefit beyond what a 24-week readout showed last year, Wave Life Sciences said on 26 March that it is on track to file its exon 53-skipping oligonucleotide candidate WVE-N531 for accelerated approval in the US in 2026.
Key Takeaways
- Wave Life Sciences intends to file its exon 53-skipping Duchenne muscular dystrophy candidate for accelerated approval next year.
The 24-week data from the FORWARD-53 trial from 24 September showed evidence of best-in-class exon skipping...
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