Berlin - Delayed Quote • EUR Daiichi Sankyo Co Ltd (D4S.BE) Follow Compare 26.62 +0.28 +(1.06%) As of 8:09:58 AM GMT+1. Market Open. Comparisons Indicators Technicals Corporate Events Chart Types Aggregated Types Draw List View Grid View Detach Attach No Tool Measure UNDO Redo All All Favorites Text Statistics Technicals Fibonacci Markings Lines Annotation Arrow Line Horizontal Vertical Rectangle Trend Line Measurement Line Average Line Callout Channel Check Continuous Crossline Elliott Wave Ellipse Doodle Fib Projection Fib Arc Fib Fan Fib Time Zone Focus Gann Fan Gartley Heart Pitchfork Quadrant Lines Ray Regression Line Fib Retracement Star Speed Resistance Arc Speed Resistance Line Time Cycle Tirone Levels Volume Profile Cross Magnet Clear All Drawings Restore Default Parameters Loading Chart for D4S.BE 1D 5D -1.66% 1M 0.64% 3M -8.30% 6M -20.75% YTD 2.27% 1Y 0.11% 5Y 28.81% All 519.07% Date Range 1 min 1 min 2 mins 3 mins 5 mins 15 mins 30 mins 1 hour 4 hours Recent News: D4S.BE View More All News Press Releases SEC Filings All SEC Filings Corporate Changes & Voting Matters Periodic Financial Reports Proxy Statements Tender Offer/Acquisition Reports Offering Registrations FDA Approves AstraZeneca's Datroway For Pretreated Breast Cancer Patients DATROWAY® Approved in the U.S. for Patients with Previously Treated Metastatic HR Positive, HER2 Negative Breast Cancer Daiichi Sankyo buys solid tumour ADC from Glycotope for $132.5m Daiichi Sankyo Acquires Intellectual Property Rights for Anti-TA-MUC1 Antibody in DS-3939 from Glycotope GmbH Datopotamab Deruxtecan Granted Priority Review in the U.S. for Patients with Previously Treated Advanced EGFR-Mutated Non-Small Cell Lung Cancer AZN, Daiichi Withdraw EU Filing for Dato-DXd in Nonsquamous NSCLC AstraZeneca, Daiichi Sankyo withdraw EU application for lung cancer treatment Datopotamab Deruxtecan Application in the EU for Patients with Advanced Nonsquamous Non-Small Cell Lung Cancer Voluntarily Withdrawn Daiichi Sankyo doses first subject in Phase III AML therapy trial AZN, Daiichi's ADC Gets FDA Breakthrough Tag for EGFR-Mutated NSCLC QuANTUM-Wild Phase 3 Trial of VANFLYTA® Initiated in Patients with Newly Diagnosed FLT3-ITD Negative AML