This phase II trial evaluates the effectiveness of sequential datopotamab deruxtecan (Dato-DXd) and trastuzumab deruxtecan (T-DXd) in treating patients with HER2-negative breast cancer that cannot be ...
Datopotamab deruxtecan demonstrated a distinct and generally manageable safety profile while delaying deterioration in several patient-reported outcomes compared with chemotherapy in previously ...
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Efficacy and safety of AKT inhibitor NTQ1062 combined with fulvestrant in patients with HR-positive/HER2-negative metastatic breast cancer:a proof-of-concept ...
What Is Datroway, and Why Does It Matter? Datroway (datopotamab deruxtecan-dlnk) is a prescription intravenous targeted cancer medicine called an antibody-drug conjugate (ADC). The FDA has approved it ...
The FDA on Friday approved datopotamab deruxtecan (Dato-DXd; Datroway) as a first-line option for unresectable or metastatic triple-negative breast cancer patients ineligible for immunotherapy.
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May 22, 2026 — AstraZeneca and Daiichi Sankyo’sDATROWAY® (datopotamab deruxtecan-dlnk) has been approved in the US for the treatment of adult patients with unresectable or metastatic triple-negative ...
ⓘ This article is third-party content and does not represent the views of this site. We make no guarantees regarding its accuracy or completeness. AstraZeneca and Daiichi Sankyo’s DATROWAY is the only ...
Datopotamab deruxtecan is now a first-line targeted therapy for immunotherapy-ineligible metastatic TNBC, addressing the ~70% lacking actionable PD-L1 eligibility and historically limited to ...
Please provide your email address to receive an email when new articles are posted on . FDA approved datopotamab deruxtecan for immunotherapy-ineligible unresectable or metastatic triple-negative ...
The FDA has approved datopotamab deruxtecan (Dato-DXd, Datroway, Daiichi Sankyo) for the treatment of patients with unresectable or metastatic triple-negative breast cancer who are not candidates for ...
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