- Sarepta Therapeutics Inc (NASDAQ:SRPT) shared new functional data across multiple studies from the SRP-9001 (delandistrogene moxeparvovec) program for Duchenne muscular dystrophy.
- SRP-9001 is an investigational gene therapy under development in partnership with Roche Holdings AG (OTC:RHHBY).
- Results from Cohort 1 demonstrated a 3.8-point improvement and 3.2-point improvement on the Duchenne functional scale 52 weeks after treatment compared to a propensity-score weighted external control.
- Related: Sarepta Therapeutics’ Shares Plummet Following FDA’s Clinical Hold On MOMENTUM Study.
- Additionally, across multiple new analyses, SRP-9001 treated patients showed statistically significant and clinically meaningful benefits versus propensity-matched external controls.
- After four years, SRP-9001-treated participants had a positive mean 7.0-point difference on the Duchenne functional scale compared to baseline.
- The safety and tolerability profile of SRP-9001 is similar to past reports. The most common treatment-related adverse event was vomiting. Increases in liver enzymes were transient and responsive to steroids.
- In Study 9001-103, there was one new serious adverse event of myocarditis in Cohort 2, resolved after one month.
- Price Action: SRPT shares are down 1.98% at $74.24 during the market session on the last check Wednesday.
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