
3 February 2026 - Daiichi Sankyo and AstraZeneca’s supplemental biologics license application for Datroway (datopotamab deruxtecan-dlnk) has been accepted and granted priority review in the US for the treatment of adult patients with unresectable or metastatic triple negative breast cancer who are not candidates for PD-1/PD-L1 inhibitor therapy.
Based on results from TROPION-Breast02 showing Daiichi Sankyo and AstraZeneca’s Datroway significantly improved overall survival versus chemotherapy in this patient population.