Eisai Co., Ltd. (TYO: 4523)

Japan flag Japan · Delayed Price · Currency is JPY
4,226.00
-14.00 (-0.33%)
Jan 20, 2025, 3:30 PM JST
-39.77%
Market Cap 1.19T
Revenue (ttm) 753.22B
Net Income (ttm) 40.97B
Shares Out 281.89M
EPS (ttm) 143.32
PE Ratio 29.49
Forward PE 23.67
Dividend 160.00 (3.77%)
Ex-Dividend Date Mar 28, 2025
Volume 574,000
Average Volume 1,469,180
Open 4,251.00
Previous Close 4,240.00
Day's Range 4,226.00 - 4,275.00
52-Week Range 4,195.00 - 7,151.00
Beta -0.13
RSI 38.62
Earnings Date Feb 7, 2025

About Eisai

Eisai Co., Ltd. engages in the research and development, manufacture, sale, and import and export of pharmaceuticals in Japan. It offers Dayvigo, for the treatment of insomnia; Lenvima, an anticancer agent/molecular targeted medicine for the treatment of thyroid cancer, renal cell carcinoma in combination with everolimus, and hepatocellular carcinoma; Methycobal for the treatment of peripheral neuropathy; and Halaven, an anticancer agent for the treatment of breast cancer. The company also provides Jyseleca, a janus kinase inhibitor; Elental, a... [Read more]

Sector Healthcare
Founded 1941
Employees 11,067
Stock Exchange Tokyo Stock Exchange
Ticker Symbol 4523
Full Company Profile

Financial Performance

In 2023, Eisai's revenue was 741.75 billion, a decrease of -0.36% compared to the previous year's 744.40 billion. Earnings were 42.41 billion, a decrease of -23.50%.

Financial Statements

News

Fujirebio and Eisai Enter into Memorandum of Understanding for Joint Research and Social Implementation of Blood-based Biomarkers in the Field of Neurodegenerative Diseases

TOKYO--(BUSINESS WIRE)-- #IVD--Fujirebio Holdings, Inc. (President & CEO: Goki Ishikawa; Head Office: Minato-ku, Tokyo), a wholly-owned subsidiary of H.U. Group Holdings, Inc. (Chairman, President and...

4 weeks ago - Business Wire

Eisai's "URECE(R)" (Dotinurad) Approved in China for Gout Patients with Hyperuricemia

TOKYO, Dec 11, 2024 - (JCN Newswire) - Eisai Co., Ltd. announced today that it has received approval for "URECE(R)" (generic name: dotinurad) from the National Medical Products Administration in China...

5 weeks ago - Benzinga

Biogen Inc (BIIB) and Eisai's Alzheimer's Drug LEQEMBI Approved in Mexico

Biogen Inc (BIIB) and Eisai's Alzheimer's Drug LEQEMBI Approved in Mexico

6 weeks ago - GuruFocus

Biogen's Outlook Dims As Analyst Projects Flat Revenue Until 2026

Needham downgraded Biogen Inc (NASDAQ: BIIB), citing limited catalysts for the company over the next year. Alzheimer’s drug Leqembi’s (lecanemab) sales growth is expected to stay gradual without a sh...

2 months ago - Benzinga

Eisai Receives Positive Opinion from the CHMP in the European Union for Lecanemab in Early Alzheimer's Disease

TOKYO and CAMBRIDGE, Mass., Nov. 14, 2024 /PRNewswire/ -- Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachuset...

2 months ago - PRNewsWire

Biogen’s stock rises after E.U. regulator reverses negative view of Alzheimer’s drug

Biogen’s stock rose 1% Thursday, after Europe’s pharmaceutical regulator issued a positive opinion on the Alzheimer’s disease drug that the company developed with Japanese partner Eisai — reversing an...

2 months ago - MarketWatch

EU drugs regulator recommends Alzheimer's drug from Eisai-Biogen

The European Union's drugs regulator on Thursday said it recommends approval of Eisai and Biogen's Leqembi in patients with early Alzheimer's disease, months after the agency first rejected the treatm...

2 months ago - Reuters

EU Backs Eisai Alzheimer’s Drug Despite Earlier Rejection

Eisai Co. and its partners won the European Union regulator’s backing for use of its Alzheimer’s drug Leqembi in a surprising reversal of a previously negative opinion.

2 months ago - BNN Bloomberg

Q2 2025 Eisai Co Ltd Earnings Presentation Transcript

Q2 2025 Eisai Co Ltd Earnings Presentation Transcript

2 months ago - GuruFocus

Eisai reports HY results

2 months ago - Seeking Alpha

Eisai updates Leqembi® outlook for fiscal year 2024 (April 2024 - March 2025). Sales now expected to reach JPY 42.5 billion

STOCKHOLM , Nov. 7, 2024 /PRNewswire/ -- BioArctic AB's (publ) (Nasdaq Stockholm: BIOA B) partner Eisai today updated their revenue outlook for Leqembi for their 2024 fiscal year (FY), which runs from...

2 months ago - PRNewsWire

Eisai Completes Rolling Submission to US FDA for LEQEMBI® (lecanemab-irmb) Biologics License Application for Subcutaneous Maintenance Dosing for the Treatment of Early Alzheimer's Disease Under the Fast Track Status

TOKYO and CAMBRIDGE, Mass. , Oct. 31, 2024 /PRNewswire/ -- Eisai Co., Ltd. (Headquarters: Tokyo , CEO: Haruo Naito , "Eisai") and Biogen Inc. (NASDAQ: BIIB , Corporate headquarters: Cambridge, Massach...

2 months ago - Benzinga

Eisai completes rolling BLA submission for subcutaneous maintenance dosing of Leqembi® (lecanemab-irmb) in the US

STOCKHOLM , Oct. 31, 2024 /PRNewswire/ -- BioArctic AB's (publ) (Nasdaq Stockholm: BIOA B) partner Eisai announced today that Eisai has completed the rolling submission of a Biologics License Applicat...

2 months ago - PRNewsWire

Leqembi® revenue totaled JPY 10 billion in the third quarter 2024

STOCKHOLM , Oct. 30, 2024 /PRNewswire/ -- BioArctic AB's (publ) (Nasdaq Stockholm: BIOA B) partner Eisai today published the preliminary global revenue for Leqembi during the third quarter 2024, in co...

2 months ago - Benzinga

Eisai will request reconsideration of initial decision for lecanemab in Australia

STOCKHOLM , Oct. 16, 2024 /PRNewswire/ -- BioArctic AB (publ) (NASDAQ Stockholm: BIOA B) partner Eisai announced today that the Therapeutic Goods Administration (TGA) of Australia issued a public stat...

3 months ago - PRNewsWire

Merck Keytruda with Eisai’s Lenvima succeeds in late-stage trial for liver cancer

Merck's (MRK) Keytruda in combination with Eisai's (ESALY) Lenvima hit main goal ina late-stage trial for liver cancer. Read more here.

4 months ago - Seeking Alpha

KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Combination With Transarterial Chemoembolization Significantly Improved Progression-Free Survival Compared to TACE Alone in Patients With Unresectable, Non-Metastatic Hepatocellular Carcinoma

In the Phase 3 LEAP-012 trial, KEYTRUDA plus LENVIMA in combination with TACE reduced the risk of disease progression or death by 34% compared to TACE alone Late-breaking first interim analysis result...

4 months ago - Benzinga

Biogen/Eisai's Leqembi Brings Hope To Early Alzheimer's Patients Amid Logistical Challenges

Biogen Inc. (NASDAQ: BIIB) and Eisai Ltd’s (OTC: ESALY) Alzheimer’s drug Leqembi (lecanemab) is reportedly offering hope for patients in the early stages of the disease despite it not being a cure. ...

4 months ago - Benzinga