Nuvalent Details Strategy to Seek First Potential Approval in 2026 and Outlines Key Anticipated 2025 Milestones
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Nuvalent plans to seek its first potential drug approval in 2026, with key milestones anticipated in 2025. The company aims to submit an NDA for zidesamtinib by mid-2025 and expects pivotal data for two drugs targeting NSCLC by the end of 2025.
January 13, 2025 | 11:45 am
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Nuvalent is targeting its first potential drug approval in 2026, with significant milestones in 2025, including an NDA submission for zidesamtinib and pivotal data for NSCLC drugs.
Nuvalent's strategy to achieve its first drug approval by 2026, with significant milestones in 2025, suggests a positive outlook for the company's future. The anticipated NDA submission and pivotal data releases are critical steps that could drive investor interest and potentially increase the stock price.
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