TOKYO & MUNICH--(BUSINESS WIRE)--Daiichi Sankyo (TSE: 4568) and AstraZeneca (LSE/STO/Nasdaq: AZN) have voluntarily withdrawn the marketing authorization application (MAA) in the EU for datopotamab ...
TOKYO & BASKING RIDGE, N.J.--(BUSINESS WIRE)--Updated results from the BEGONIA phase 1b/2 trial for the cohort of patients treated with datopotamab deruxtecan (Dato-DXd) plus durvalumab (Arm 7) showed ...
Please provide your email address to receive an email when new articles are posted on . Datopotamab deruxtecan failed to extend OS vs. chemotherapy for adults with advanced breast cancer, according to ...
WILMINGTON, Del.--(BUSINESS WIRE)-- AstraZeneca and Daiichi Sankyo’s Biologics License Application (BLA) for datopotamab deruxtecan (Dato-DXd) has been accepted and granted Priority Review in the US ...
Datopotamab deruxtecan significantly improves overall survival compared with chemotherapy in previously untreated metastatic TNBC. The Food and Drug Administration (FDA) has accepted for Priority ...
Findings showed datopotamab deruxtecan significantly improved PFS and OS vs chemotherapy. Topline data were announced from a phase 3 trial evaluating datopotamab deruxtecan-dlnk as a first-line ...
High-level overall survival (OS) results from the TROPION-Lung01 phase III trial, which previously met the dual primary endpoint of progression-free survival (PFS), numerically favoured datopotamab ...
Datopotamab deruxtecan not only demonstrated a statistically significant improvement over chemotherapy for breast cancer and docetaxel for non–small cell lung cancer (NSCLC), but the intervention ...
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