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Market Cap 18.67B P/E 46.71 EPS this Y - Ern Qtrly Grth -30.90%
Income 45.42B Forward P/E - EPS next Y - 50D Avg Chg -4.00%
Sales 749.46B PEG - EPS past 5Y - 200D Avg Chg 5.00%
Dividend 1,012.00% Price/Book 0.02 EPS next 5Y - 52W High Chg -24.00%
Recommedations - Quick Ratio 1.70 Shares Outstanding 1.15B 52W Low Chg 20.00%
Insider Own - ROA 3.03% Shares Float 272.92M Beta -0.06
Inst Own 0.03% ROE 5.70% Shares Shorted/Prior -/- Price 15.88
Gross Margin 78.95% Profit Margin 6.06% Avg. Volume 69,758 Target Price -
Oper. Margin 3.44% Earnings Date May 14 Volume 26,058 Change 0.44%
About EISAI CO UNSPON ADS EACH REP 1

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 branched-chain amino acid preparation; Goofice and Movicol for chronic constipation; Fycompa, an antiepileptic agent; Pariet, a proton-pump inhibitor; Aricept, for Alzheimer's disease/Dementia with Lewy bodies; and Chocola BB plus for the preparation vitamin B2. Eisai Co., Ltd. was formerly known as Nihon Eisai Co., Ltd. and changed its name to Eisai Co., Ltd. in 1955. Eisai Co., Ltd. was incorporated in 1941 and is headquartered in Tokyo, Japan.

EISAI CO UNSPON ADS EACH REP 1 News
04/24/24 Alzheimer’s Drug Leqembi Sees Sales Pickup, Boosting Biogen Stock
03/31/24 Eisai Completes Submission of LEQEMBI® (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer's Disease to the U.S. FDA
10/27/23 Alzheimer's drug Leqembi: The twice-monthly infusion could be available in injection form
10/26/23 Eisai reporting positive data on injectable Alzheimer’s drug
10/25/23 EISAI PRESENTS NEW LEQEMBI® (LECANEMAB-IRMB) INVESTIGATIONAL SUBCUTANEOUS FORMULATION INTERIM STUDY RESULTS AND CLINICAL IMPROVEMENT DATA IN EARLIER STAGES OF EARLY ALZHEIMER'S DISEASE FROM ADDITIONAL ANALYSES OF CLARITY AD AT THE CLINICAL TRIALS ON ALZHEIMER'S DISEASE (CTAD) CONFERENCE
09/24/23 Eisai's Alzheimer's drug Leqembi gets green light in Japan, shares surge
07/19/23 Eisai Presents Latest Analysis of Lecanemab's Effect on Biomarker Changes and Subcutaneous Dosing at The Alzheimer's Association International Conference (AAIC) 2023
07/18/23 New Alzheimer's drug success 'was built on failures': Eisai exec
07/11/23 EISAI TO PRESENT THE LATEST ALZHEIMER'S DISEASE PIPELINE AND RESEARCH, INCLUDING LECANEMAB AND ANTI-MTBR TAU ANTIBODY E2814, AT THE ALZHEIMER'S ASSOCIATION INTERNATIONAL CONFERENCE (AAIC) 2023
07/07/23 Biogen, Eisai stocks fall despite receiving FDA approval for Alzheimer's drug
07/07/23 New Alzheimer's drug from Biogen, Eisai gets government approval, but faces long road ahead
07/07/23 Eisai-Biogen's Alzheimer's treatment drug receives FDA approval
07/06/23 FDA Grants Traditional Approval for LEQEMBI® (lecanemab-irmb) for the Treatment of Alzheimer's Disease
06/09/23 FDA Advisory Committee Votes Unanimously to Confirm the Clinical Benefit of LEQEMBI® (lecanemab-irmb) for the Treatment of Alzheimer's Disease