Investing.com - Novocure (NASDAQ: NVCR) stock surged over 30% in after-hours trading on Wednesday after the U.S. Food and Drug Administration approved the company’s Optune Pax device for the treatment of locally advanced pancreatic cancer.
This wearable device, used in combination with the chemotherapy drug gemcitabine and albumin-bound paclitaxel, delivers tumor-treating electric fields (TTFields). These alternating electric fields are designed to disrupt cancer cell division and trigger cell death, while not significantly damaging healthy tissue.
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The company’s stock rose more than 30% to $13.80 before 8:19 a.m. Eastern Time (8:19 p.m. Beijing time), after initially climbing over 50% in after-hours trading.
The approval was based on results from the Phase 3 PANOVA-3 clinical trial, which enrolled 571 patients.
The study also showed that the device significantly delayed pain progression and improved one-year survival rates, with safety profiles comparable between the two treatment groups.
This article was translated with the assistance of artificial intelligence. For more information, please see our Terms of Use.
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Novocure stock soars 30% after FDA approves pancreatic cancer device
Investing.com - Novocure (NASDAQ: NVCR) stock surged over 30% in after-hours trading on Wednesday after the U.S. Food and Drug Administration approved the company’s Optune Pax device for the treatment of locally advanced pancreatic cancer.
This wearable device, used in combination with the chemotherapy drug gemcitabine and albumin-bound paclitaxel, delivers tumor-treating electric fields (TTFields). These alternating electric fields are designed to disrupt cancer cell division and trigger cell death, while not significantly damaging healthy tissue.
Subscribe to InvestingPro for quick Wall Street updates
The company’s stock rose more than 30% to $13.80 before 8:19 a.m. Eastern Time (8:19 p.m. Beijing time), after initially climbing over 50% in after-hours trading.
The approval was based on results from the Phase 3 PANOVA-3 clinical trial, which enrolled 571 patients.
The study also showed that the device significantly delayed pain progression and improved one-year survival rates, with safety profiles comparable between the two treatment groups.
This article was translated with the assistance of artificial intelligence. For more information, please see our Terms of Use.