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The FDA's acceptance of the NDA signals strong potential for VSTM's future sales, similar to past FDA approvals boosting similar biotech stocks.
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FDA accepted Verastem's NDA for avutometinib with defactinib. Combination targets recurrent low-grade ovarian cancer with KRAS mutation. NDA received Priority Review; action date is June 30, 2025. Phase 2 trial showed durable response rates in patients. Ongoing trials may expand indications beyond KRAS mutations.
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