Eisai Co Ltd

Discover how Eisai’s EMA IV‑maintenance and FDA SC‑autoinjector approvals could improve Alzheimer’s therapy access, boost patient adherence, and expand market reach.

Priority review for Eisai’s Leqembi autoinjector accelerates at‑home Alzheimer’s treatment, boosting patient convenience, potential market share, and strategic momentum.

Explore how Eisai’s diversified portfolio and breakthrough trials are boosting investor confidence, with highlights on Alzheimer’s, oncology and neuroinflammation research.

Explore Eisai’s dual pharma‑and‑agro strategy, growth prospects, and risks—from oncology trials to green pesticides—insights for investors.

New Eisai data shows anti‑tau antibody etalanetug reduces tau PET signal in some DIAD patients and a subcutaneous Leqembi launch targets Japan, boosting AD treatment access and convenience.

Discover how Eis Co.’s subcutaneous Leqembi (lecanemab) filings in Japan & the U.S. aim to accelerate Alzheimer’s therapy access, boost market share, and secure IP protection.

Read how Eisai’s Leqembi Iqlik could change Alzheimer’s care with at‑home injections and the implications for FDA approval, pricing, and market growth.

Shares of Eisai surge 6.4% as Nikkei rebounds, driven by strong biotech pipeline—Aduhelm, Lenvima, Inovelge—and upbeat market expectations for rate cuts.

Eisai Co., Ltd. has received FDA fast-track designation for its investigational Alzheimer’s disease treatment, a move that could accelerate its development and approval process, and position the company as a leader in the neurodegenerative disease m…

Eisai Co Ltd’s stock price surged 4.07% to a new high after the US FDA approved its Alzheimer’s treatment, LEQEMBI IQLIK, for maintenance dosing, marking a significant milestone for the company.