Creating value through cutting-edge science and an unwavering commitment to patients
At Sarepta, we are leading a revolution in precision genetic medicine and every day is an opportunity to change the lives of people living with rare disease. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing.
Our work is purposeful, audacious, urgent. Our commitment to do well by patients is unyielding as we build our position as the world's leader in precision genetic medicine.
|5/31/23||Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)|
|5/24/23||Sarepta Therapeutics Announces Update on Regulatory Review of SRP-9001|
|5/12/23||Sarepta Therapeutics Announces Positive Vote from U.S. FDA Advisory Committee Meeting for SRP-9001 Gene Therapy to Treat Duchenne Muscular Dystrophy|
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