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FDA Approves NovoCure’s Optune Pax for Locally Advanced Pancreatic Cancer

The decision delivers the first new treatment option for this patient group in decades based on survival gains in a pivotal trial.

Overview

  • The FDA cleared Optune Pax for adult patients with locally advanced pancreatic cancer after the Phase 3 PANOVA-3 trial showed a statistically significant overall survival benefit versus chemotherapy alone in 571 patients.
  • NovoCure shares jumped about 29% in pre-market trading following the approval, though the stock remains down roughly 19% year to date and 52% over the past 12 months.
  • Regulatory clearance arrived roughly a quarter earlier than analysts expected, giving the company extra time to build inventory and negotiate reimbursement with insurers.
  • Optune Pax is used with gemcitabine and nab-paclitaxel and uses a biophysical approach that targets the electrical properties of cancer cells.
  • H.C. Wainwright raised its price target to $47 and increased its pancreatic success probability to 100% while maintaining a Buy rating.