FDA grants accelerated approval to the combination of avutometinib and defactinib for KRAS-mutated recurrent low-grade serous ovarian cancer

FDA

8 May 2025 - Today, the FDA granted accelerated approval to the combination of avutometinib and defactinib (Avmapki Fakzynja Co-pack, Verastem) for adults with KRAS mutated recurrent low grade serous ovarian cancer who have received prior systemic therapy.

Efficacy was evaluated in RAMP-201, an open-label, multi-centre trial that included 57 adults with measurable KRAS mutated recurrent low grade serous ovarian cancer.

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Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , US , Registration