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Gilead expands EU approval of Trodelvy with Keytruda for TNBC

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Sig4.20Sen+5.10Env0.00Soc+2.40Gov+0.30

Gilead Sciences received expanded European Commission approval for Trodelvy combined with Keytruda as a first-line treatment for metastatic triple-negative breast cancer across PD-L1 status in Europe. The decision makes Trodelvy plus Keytruda the first approved antibody-drug conjugate and immunotherapy combination for first-line metastatic TNBC across the EU, strengthening Gilead’s oncology trajectory in the region.

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