FDA Approves Avmapki Fakzynja Co-Pack for KRAS-Mutated Recurrent Low-Grade Serous Ovarian Cancer

The Food and Drug Administration (FDA) approved the Avmapki Fakzynja Co-Pack as the first treatment for adult patients with KRAS-mutated recurrent low-grade serous ovarian cancer who have previously undergone systemic therapy. This approval marks a new option for a specific subset of ovarian cancer patients. Specifically, the FDA approval applies to adult patients whose low-grade serous ovarian cancer has recurred and carries a KRAS mutation. Furthermore, these patients must have already received prior systemic treatment for their cancer. The Avmapki Fakzynja Co-Pack offers a treatment option in cases where previous therapies have not been successful.

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Date: May 9, 2025

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Author

Mark Chiang

紐約 NYU Computer Science 碩士 紐澤西 UMDNJ Biomedical Informatics 博士 中研院博士後 台灣大學博士後