Reported Wednesday, China's NMPA Approves GenFleet And Verastem Oncology's GFH375 For KRAS G12D Phase I/II Trials
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China's NMPA has approved GenFleet Therapeutics and Verastem Oncology's GFH375 for Phase I/II trials targeting advanced solid tumors with the KRAS G12D mutation. This mutation is prevalent in human cancers, and no targeted therapies have been approved yet.
June 20, 2024 | 9:45 am
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Verastem Oncology's GFH375 has been approved by China's NMPA for Phase I/II trials targeting the KRAS G12D mutation in advanced solid tumors. This approval could lead to significant advancements in cancer treatment.
The approval by China's NMPA for Phase I/II trials is a significant milestone for Verastem Oncology. It opens the door for potential advancements in treating cancers with the KRAS G12D mutation, which is highly prevalent and currently lacks targeted therapies. This could positively impact Verastem's stock price in the short term.
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