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Findings from HERTHENA-Lung02 showed that the key secondary endpoint of overall survival did not meet statistical significance.
Susan Galbraith of AstraZeneca and Ken Takeshita of Daiichi Sankyo echoed the sentiment, highlighting the potential for ENHERTU to transform the treatment landscape and delay disease progression.
Results from three trials continue to demonstrate the potential of DATROWAY® (datopotamab deruxtecan) in combination with ...
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Pharmaceutical Technology on MSNDaiichi Sankyo and MSD withdraw US BLA for lung cancer treatmentDaiichi Sankyo and MSD have voluntarily withdrawn the biologics licence application (BLA) in the US for their HER3-directed ...
Daiichi Sankyo research and development global head Ken Takeshita said: “While we are disappointed with the OS results of HERTHENA-Lung02, we are conducting further biomarker analyses to better ...
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Stocktwits on MSNMerck, Daiichi Sankyo Pull FDA Application For Lung Cancer Therapy: Retail Terms It A ‘Huge Flop’(MRK) and Daiichi Sankyo on Thursday said that the companies have withdrawn their application to the U.S. Food and Drug ...
(RTTNews) - The Biologics License Application (BLA) seeking accelerated approval of patritumab deruxtecan, co-developed by Merck & Co Inc. (MRK) and Daiichi ... said Ken Takeshita, Global Head ...
“EGFR-mutated non-small cell lung cancer has proven to be difficult-to-treat in the second-line metastatic setting and beyond,” said Ken Takeshita, MD, Global Head, R&D, Daiichi ...
When Merck & Co. and Daiichi Sankyo last year received an FDA complete ... multiple clinical trials across 15 types of cancer," Ken Takeshita, M.D., Daiichi's global head of R&D, said in a statement.
"EGFR-mutated non-small cell lung cancer has proven to be difficult-to-treat in the second-line metastatic setting and beyond," said Ken Takeshita, MD, Global Head, R&D, Daiichi Sankyo. "While we are ...
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