The FDA last month accepted the application for subcutaneous Leqembi for maintenance dosing, with a target action date of ...
The EC requests CHMP to reassess new safety data that emerged after the positive opinion recommending the approval of ...
Biogen BIIB and Japan-based partner, Eisai, announced an update regarding the regulatory review of an application seeking the approval of Leqembi (lecanemab) for mild cognitive impairment due to ...
We recently compiled a list of the 12 Best S&P 500 Stocks to Invest in According to Analysts. In this article, we are going ...
Japan’s Eisai and US partner Biogen have announced today update on the ongoing regulatory review of the Marketing Authorization Application for lecanemab (trade name Leqembi) as a treatment for early ...
On January 26, Eisai Co., Ltd. and Biogen announced that the U.S. Food and Drug Administration (FDA) has approved once every four weeks maintenance dosing of Alzheimer’s drug, LEQEMBI.