Eisai Named to List of The Time 100 Most Influential Companies
03.06.2024 - 10:16:38
LEQEMBI is the first and only treatment approved in Japan, the United States, China, and South Korea shown to reduce the rate of disease progression and to slow cognitive and functional decline, that acts on the underlying pathology of AD.
AD is a progressive, fatal disease, and a global healthcare issue that greatly impacts not only the people living with the disease, but also their loved ones, care partners and society. Based on our corporate concept of "human health care (hhc)," we have taken on the challenge of this difficult issue through our nearly 40 years of drug discovery activities in the field of dementia, while spending time with patients and their families. We will deliver LEQEMBI to the people with early AD who need it and their families, and aim to continue creating impact on global issues surrounding dementia.
Eisai serves as the lead of LEQEMBI development and regulatory submissions globally with both Eisai and Biogen Inc. (U.S.) co-commercializing and co-promoting the product and Eisai having final decision-making authority.
Please see full Prescribing Information (www.leqembi.com/-/media/Files/Leqembi/Prescribing-Information.pdf), including Boxed WARNING in the United States.
MEDIA CONTACTS:
Eisai Co., Ltd.
Public Relations Department
TEL: +81 (0)3-3817-5120
Source: Eisai
Copyright 2024 JCN Newswire . All rights reserved.
AD is a progressive, fatal disease, and a global healthcare issue that greatly impacts not only the people living with the disease, but also their loved ones, care partners and society. Based on our corporate concept of "human health care (hhc)," we have taken on the challenge of this difficult issue through our nearly 40 years of drug discovery activities in the field of dementia, while spending time with patients and their families. We will deliver LEQEMBI to the people with early AD who need it and their families, and aim to continue creating impact on global issues surrounding dementia.
Eisai serves as the lead of LEQEMBI development and regulatory submissions globally with both Eisai and Biogen Inc. (U.S.) co-commercializing and co-promoting the product and Eisai having final decision-making authority.
Please see full Prescribing Information (www.leqembi.com/-/media/Files/Leqembi/Prescribing-Information.pdf), including Boxed WARNING in the United States.
MEDIA CONTACTS:
Eisai Co., Ltd.
Public Relations Department
TEL: +81 (0)3-3817-5120
Source: Eisai
Copyright 2024 JCN Newswire . All rights reserved.

