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Aug 24, 2026 12:25 PM ET
Signal
FDA/Bio
European Commission Expands Role of Gilead’s Trodelvy® in First-Line Metastatic Triple-Negative Breast Cancer Across PD-L1 Status
EU approval expands Trodelvy’s first-line use across all PD-L1 statuses, boosting market access.
What changed
Why it matters
EU approval expands Trodelvy’s first-line use across all PD-L1 statuses, boosting market access.
Sources
eodhd
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