Reports Q2 revenue $611.1M, cocnensus $531.04M. “We are very pleased that following a rapid review of the safety data, the FDA swiftly recommended that we take the ambulatory patient population off shipment pause and, following that, we have already resumed deliveries. Infusions are taking place for the ambulatory community. We will continue to work with the FDA to define the path and develop the risk mitigation necessary to bring ELEVIDYS back to the non-ambulatory community as well,” said Doug Ingram, chief executive officer, Sarepta (SRPT). “With the temporary pause lifted, the execution of our restructuring, cost savings and plans designed to meet our financial obligations, and with important siRNA readouts expected later this year, we are well positioned to achieve our strategic objective to remain a patient-centric, financially disciplined organization into the next decade and beyond.”
Elevate Your Investing Strategy:
- Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on SRPT:
- RBC says two new deaths listed in FAERS data for Sarepta’s Elevidys
- Vor Bio appoints Murray as Chief Commercial Officer
- D-Wave, Sarepta, Cadence, Albemarle, CyberArk: Trending by Analysts
- Buy/Sell: Wall Street’s top 10 stock calls this week
- Sarepta Stock (SRPT) Rallies on FDA Nod for Broader Gene Therapy Use