Available in United States, Brazil, Spain
The study will investigate the efficacy and safety of Dato-DXd with or without durvalumab
when compared with ICT (capecitabine and/or pembrolizumab) in participants with stage I
to III TNBC who have residual invasive disease in the breast and/or axillary lymph nodes
at surgical resection following neoadjuvant systemic therapy.
The primary objective of the study is to demonstrate superiority of Dato-DXd in
combination with durvalumab relative to ICT by assessment of iDFS in participants with
stage I to III TNBC with residual invasive disease at surgical resection following
neoadjuvant therapy.
1075Patients around the world