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AstraZeneca, european medicines agency and lung cancer
AstraZeneca withdraws application for lung cancer drug in EU
AstraZeneca has voluntarily withdrawn its marketing authorisation application with the EU's medicines regulator for its experimental precision drug for the treatment of a type of lung cancer, it said on Tuesday.
AstraZeneca, Daiichi Sankyo Withdraw Authorization Application for Lung Cancer Treatment in EU
AstraZeneca said it and Daiichi Sankyo decided to voluntarily withdraw the marketing authorization application in the European Union for advanced lung-cancer treatment Dato-DXd. This decision followed a feedback from the European Medicines Agency, the pharma company said Tuesday.
AstraZeneca And Daiichi Sankyo Withdraw EU Marketing Application For Datopotamab Deruxtecan
British drug maker AstraZeneca Plc (AZN.L, AZN) and Daiichi Sankyo (DSKYF.PK) said that they have voluntarily withdrawn their
AstraZeneca, Daiichi pull EU marketing application for lung cancer drug, Dato-DXd
AstraZeneca (NASDAQ:AZN) and Daiichi Sankyo (OTCPK:DSKYF) announced Tuesday they have withdrawn the EU marketing application for their experimental lung cancer therapy, datopotamab deruxtecan (Dato-DXd),
1d
on MSN
European markets close higher ahead of Christmas shutdown; Novo Nordisk resumes recovery
European markets are set to open higher on Tuesday, in a shortened trading session for Christmas Eve. London's FTSE 100 is ...
1d
Sickle cell disease drug's withdrawal leads to suits against Pfizer
A once-groundbreaking sickle cell disease drug — at the center of a $5.4 billion acquisition two years ago — is the subject ...
1d
on MSN
Anavex stock rallies 30% on business updates
Anavex (AVXL) stock rallied 30% Monday after the company announced EU regulators had accepted the market application for its ...
Daily
7h
Bristol Myers Squibb gets European Commission nod for Opdivo plus Yervoy to treat colorectal cancer
Princeton: Bristol Myers Squibb has announced that the European Commission (EC) has approved Opdivo (nivolumab) plus Yervoy ...
2d
Cytokinetics announces EMA has validated MAA for aficamten
Cytokinetics (CYTK) announced that the European Medicines Agency, EMA, has validated the Marketing Authorization Application, MAA, for ...
devdiscourse
1d
Biocon and Zentiva Secure EU Approval for Diabetes and Weight Management Drug
Biocon Ltd, in collaboration with Zentiva, has obtained EU approval for the complex formulation Liraglutide, a generic ...
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