Nuvalent reported its Q4 and full year 2023 financial results, highlighting pipeline progress and reiterating key anticipated milestones. The company's cash position is expected to fund operations into 2027.
FDA granted breakthrough therapy designation to NVL-520 for ROS1-positive metastatic non-small cell lung cancer (NSCLC).
Phase 2 portion of ALKOVE-1 trial of NVL-655 initiated for advanced ALK-positive NSCLC.
Updated data from ARROS-1 and ALKOVE-1 trials expected to be shared at medical meetings in 2024.
Phase 1 trial for HER2 program expected to be initiated in 2024.
Nuvalent plans to execute on global registrational strategies, progress the Phase 2 portions of its ARROS-1 and ALKOVE-1 trials, launch the front-line development strategy for its ALK program, present interim data from ongoing clinical trials, and initiate the Phase 1 trial for its HER2 program.