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Enhertu granted Priority Review in the US for patients with metastatic HER2-positive solid tumours

AstraZeneca and Daiichi Sankyo's supplemental Biologics License Application (sBLA) for Enhertu (trastuzumab deruxtecan) has been accepted and granted Priority Review in the US for the treatment of adult patients with unresectable or metastatic HER2-positive (immunohistochemistry [IHC] 3+) solid tumours who have ...
United Kingdom United States Trastuzumab Deruxtecan Susan Galbraith Daiichi Sankyo Enhertu Ken Takeshita

Datopotamab deruxtecan significantly extended progression-free survival vs. chemotherapy in patients with HR-positive, HER2-low or negative breast cancer in TROPION-Breast01 Phase III trial

AstraZeneca and Daiichi Sankyoโ€™s datopotamab deruxtecan reduced the risk of disease progression or death by 37%, providing a 2-month median PFS benefit, and was well tolerated in post-endocrine...
United States United Kingdom Daiichi Sankyo End Results Program European Society For Medical Oncology Sapporo Medical University

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Datopotamab deruxtecan demonstrated statistically significant and clinically meaningful progression-free survival benefit in patients with HR-positive, HER2-low or negative breast cancer in TROPION-Breast01 Phase III trial

First Phase III results in breast cancer for AstraZeneca and Daiichi Sankyoโ€™s datopotamab deruxtecan Plans for global regulatory submissions underway ...
United Kingdom United States Ken Takeshita Daiichi Sankyo Susan Galbraith Merck Co Inc

ENHERTU® (fam-trastuzumab deruxtecan-nxki) demonstrated clinically meaningful and durable responses in patients across multiple HER2-expressing advanced solid tumors

AstraZeneca and Daiichi Sankyo’s ENHERTU showed an objective response rate of 37.1% in the overall population of the DESTINY-PanTumor02 Phase II trial ENHERTU is the first therapy to show... | June 5, 2023
United States United Kingdom Cristian Massacesi Daiichi Sankyo Van Cutsem Mark Rutstein

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