🇺🇸·3h agoIndustry
FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), each with Trodelvy® (sacituzumab govitecan-hziy) as First-Line Treatment of PD-L1+ (CPS ≥10) Advanced Triple-Negative Breast Cancer (TNBC)
Publisher
M
Merck & Co. (MSD) News
USA
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- Publisher
- Merck & Co. (MSD) News
- Region
- USA
- Scope
- Industry
- Published
- June 25, 2026
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Source: Merck & Co. (MSD) News
Scope: Industry
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