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Information about pipeline compounds or investigational uses of compounds does not imply FDA approval for these compounds or uses, nor does it establish the safety or efficacy of these compounds or uses. There is no guarantee that the pipeline compounds or investigational uses will receive FDA approval. Daiichi Sankyo does not recommend or suggest use of its medicines in a manner inconsistent with FDA-approved labeling.
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T-DXd
Trastuzumab deruxtecan in previously treated HER2-positive gastric cancer: A plain language summary of the DESTINY-Gastric01 study
Dato-DXd
Application of the model-informed drug development paradigm to datopotamab deruxtecan dose selection for late-stage development
Edoxaban
Echocardiographic parameters of left atrial structure and function and clinical outcomes at 2 years in elderly patients with atrial fibrillation — The ANAFIE echocardiographic substudy
Edoxaban
Impact of cognitive impairment on clinical outcomes in elderly patients with atrial fibrillation: ANAFIE registry
T-DXd
Efficacy and safety of trastuzumab deruxtecan in patients with HER2-expressing solid tumors: Primary results from the DESTINY-PanTumor02 phase II trial
T-DXd
Analytical and clinical validation of PATHWAY Anti-HER-2/neu (4B5) antibody to assess HER2-low status for trastuzumab deruxtecan treatment in breast cancer
Edoxaban
Direct oral anticoagulant dosing in patients with atrial fibrillation: An Asian perspective
T-DXd
Treatment with trastuzumab deruxtecan in patients with HER2-positive breast cancer and brain metastases and/or leptomeningeal disease (ROSET-BM)
Pexidartinib
Supporting patients in the transition to the revised pexidartinib dosing regimen: Perspectives from the multidisciplinary clinical and allied health professional team
HER3-DXd
Patritumab deruxtecan (HER3-DXd), a human epidermal growth factor receptor 3-directed antibody-drug conjugate, in patients with previously treated human epidermal growth factor receptor 3-expressing metastatic breast cancer: A multicenter, phase I/II trial