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European Medicines Agency Validates Bristol Myers Squibb's Application for Repotrectinib for the Treatment of Locally Advanced or Metastatic ROS1-Positive Non-Small Cell Lung Cancer and NTRK-Positive Solid Tumors -January 02, 2024 at 07:00 am EST

Application based on data from the registrational TRIDENT-1 and CARE trials showing robust responses and durable activity in these patient populations If approved, repotrectinib will offer a...
United States Joseph Fiore Bristol Myers Squibb Bristol Myers Squibb Company European Medicines Agency Drug Administration

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