Japan`s Eisai developing dementia drug for US market, Nikkei reports
Ensho Therapeutics has emerged with an inflammatory disease therapy portfolio from Eisai’s GI subsidiary EA Pharma, including a phase 2-ready clinical program in ulcerative colitis (UC).
Lilly Alzheimer`s drug gets unanimous backing from FDA advisory panel
FDA accepts Eisai`s monthly dosing application for Leqembi
TOkYO and CAMBRIDGE, Mass., June 09, 2024 (GLOBE NEWSWIRE) -- Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge,...
Bloomberg Intelligence analysts expect Eli Lilly to come from behind and capture half of a $13 billion market by 2030.
US FDA staff raise no major concerns about Eli Lilly Alzheimer`s drug
Japan-headquartered pharmaceutical firm Eisai Co. and US-based Biogen Inc. have announced that the Ministry of Food and Drug Safety (MFDS) in South Korea has approved humanised anti-soluble aggregated amyloid-beta (A?) monoclonal antibody LEQEMBI (lecanemab) for treatment in adult patients with mild cognitive impairment due to Alzheimer’s disease (AD) or mild AD (early AD).
NUTLEY, N.J., May 23, 2024 /PRNewswire/ -- Eisai announced today the presentation of research across multiple types of cancer from its oncology portfolio and pipeline during the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting (#ASCO24), which is taking place virtually and in-person in Chicago, Illinois from May 31 to June 4.
Eisai Co. and nippon medac Co., a subsidiary of medac group, have launched the anti-rheumatic agent 'Metoject Subcutaneous Injection 7.5mg Pen 0.15mL, 10mg Pen 0.20mL, 12.5mg Pen 0.25mL and 15mg Pen 0.30mL' (methotrexate, or MTX), in Japan.