Brief: FDA Says CDER Proposed To Withdraw Approval Of Tavneos
April 27 (Reuters) - Amgen Inc AMGN.O: FDA: CDER PROPOSES TO WITHDRAW APPROVAL OF TAVNEOS FDA: NEW INFORMATION INDICATES THAT TAVNEOS HAS NOT BEEN SHOWN TO BE EFFECTIVE FOR ITS APPROVED USE FDA: TAVNEOS WILL REMAIN ON THE MARKET UNTIL THE APPLICANT DECIDES TO REMOVE THE DRUG OR THE FDA COMMISSIONER MANDATES ITS REMOVAL Source text: https://tinyurl.com/2abqou95 Further company coverage: AMGN.O ((Reuters.Briefs@thomsonreuters.com;))
Recent news on Amgen
See all newsFactbox: Global drugmakers invest billions to boost US presence
China's Harbour BioMed to focus on another patent case after $20 million damages award
Amgen owes $20.2 million in antibody patent lawsuit, US jury says (updated)
Amgen owes $20.2 mln in antibody patent lawsuit, US jury says
Amgen taps research firm to reassess Tavneos data (updated)