Eu, Eisai and Biogen
Biogen and Eisai said they believe that EC's requests can be addressed with existing information, and that no new safety signals have been identified for Leqembi. The U.S. Food and Drug Administration ...
The US Food and Drug Administration has approved the supplemental biologics licence application (sBLA) of Eisai and Biogen's ...
Merck's blockbuster drug Keytruda and Eisai's cancer drug Lenvima, in combination with chemotherapy, failed to improve ...
The monthly maintenance regimen, which offers a more convenient frequency than the initially approved treatment schedule for ...
Merck & Co. and Eisai have to deal with the reality that yet another phase 3 trial of their combination of Keytruda and ...
GlobalData on MSN7d
MSD and Eisai’s LEAP gastroesophageal cancer trial sees mixed successMSD and Eisai’s trial saw mixed success with its two primary endpoints, seeing success in progression-free survival, but ...
In the latest development, the European Commission has asked the EMA's human medicines committee, the CHMP, to take a look at ...
Several medicines are poised to reach new heights after winning key endorsements from European drug regulators. | Among those ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback