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News

Nuvalent Secures FDA Breakthrough Therapy Designation For NVL-520

Author: Benzinga Newsdesk | February 27, 2024 07:17am

The BTD for NVL-520 is based on the preliminary safety and activity of NVL-520 in heavily pretreated patients with advanced ROS1-positive NSCLC in the Phase 1 portion of the Phase 1/2 ARROS-1 clinical trial. Enrollment in the Phase 2 portion of the trial is ongoing, and the company expects to share updated data from the trial at a medical meeting in 2024.

Posted In: NUVL