European Commission expands Trodelvy use in metastatic breast cancer
The European Commission expands the role of Gilead’s Trodelvy in first-line metastatic triple-negative breast cancer across PD-L1 status.
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The European Commission expands the role of Gilead’s Trodelvy in first-line metastatic triple-negative breast cancer across PD-L1 status.
The European Commission grants marketing authorization for Gilead’s Trodelvy with Keytruda in first-line PD-L1-positive metastatic triple-negative breast cancer and expands its role across PD-L1 status.