Nuvalent, Inc. announced the completion of its NDA submission for zidesamtinib

On September 22, 2025, Nuvalent, Inc. reported the completion of its New Drug Application submission to the U.S. Food and Drug Administration for zidesamtinib in tyrosine kinase inhibitor pre-treated patients with advanced ROS1-positive non-small cell lung cancer (Press release, Nuvalent, SEP 22, 2025, View Source [SID1234656148]).

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