Information in the news releases is current on the date of the announcement, but is subject to change without prior notice.
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December 18, 2020
EISAI COMPLETES CONSTRUCTION OF THE 5TH MANUFACTURING BUILDING AT KAWASHIMA INDUSTRIAL PARK IN JAPAN
TO STRENGTHEN ITS IN-HOUSE PRODUCTION FUNCTION FOR FORMULATING ANTI-CANCER AGENT LENVIMA®
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December 16, 2020
LENVIMA® (lenvatinib) Plus KEYTRUDA® (pembrolizumab) Combination Demonstrated Statistically Significant Improvement in Overall Survival, Progression-Free Survival and Objective Response Rate Versus Chemotherapy in Patients With Advanced Endometrial Cancer Following Prior Systemic Therapy in Phase 3 Study
First Overall Survival Analysis for LENVIMA Plus KEYTRUDA Combination in a Phase 3 Study in Advanced Endometrial Cancer
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December 10, 2020
BIOGEN FILES NEW DRUG APPLICATION FOR ADUCANUMAB IN JAPAN
If approved, aducanumab would become the first treatment to meaningfully change the course of Alzheimer’s disease
Aducanumab is now under regulatory review in Japan, Europe and the United States
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December 4, 2020
EISAI TO PRESENT ABSTRACTS ON ONCOLOGY PRODUCTS AND PIPELINE AT 43RD ANNUAL SAN ANTONIO BREAST CANCER SYMPOSIUM
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November 30, 2020
EISAI AND WREN THERAPEUTICS ENTER INTO RESEARCH COLLABORATION AGREEMENT FOR DRUG DISCOVERY FOR SYNUCLEINOPATHIES
This collaboration aims to develop a disease modifying treatment for synucleinopathies based on network kinetics ofα-synuclein misfolding and aggregation
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November 30, 2020
EISAI TO PRESENT LATEST DATA ON PERAMPANEL AT THE 74TH AMERICAN EPILEPSY SOCIETY ANNUAL MEETING
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November 27, 2020
AbbVie and Eisai Announce an approval for additional indication of HUMIRA®, a fully Human Anti-TNFα Monoclonal Antibody, for the treatment of pyoderma gangrenosum for the first time in the world
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November 26, 2020
EISAI COMMENCES “PaDiCo” SMARTPHONE APPLICATION SERVICE IN JAPAN TO SUPPORT THE DAILY LIVES OF PATIENTS WITH PARKINSON’S DISEASE
WITH SIMPLE OPERATION, APP RECORDS AND VISUALIZES SYMPTOMS TO SUPPORT COMMUNICATION BETWEEN PATIENTS AND DOCTORS
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November 18, 2020
EISAI SELECTED FOR MEMBERSHIP IN DOW JONES SUSTAINABILITY ASIA PACIFIC INDEX 2020 FOR SEVENTH TIME
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November 18, 2020
JYSELECA® (FILGOTINIB) FOR RHEUMATOID ARTHRITIS LAUNCHES IN JAPAN
A once-daily, oral, JAK inhibitor for the treatment of rheumatoid arthritis in patients who have had an inadequate response to conventional therapies
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November 16, 2020
EISAI RECEIVES APPROVAL FOR INDICATION EXPANSION OF ANTI-EPILEPTIC AGENT FYCOMPA® FOR USE IN PEDIATRIC PATIENTS
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November 10, 2020
LENVIMA® Plus KEYTRUDA® Demonstrated Statistically Significant Improvement in Progression-Free Survival, Overall Survival and Objective Response Rate Versus Sunitinib as First-Line Treatment for Patients With Advanced Renal Cell Carcinoma
LENVIMA® Plus Everolimus Also Showed Statistically Significant Improvement in PFS and ORR Endpoints Versus Sunitinib
Results of Investigational Phase 3 CLEAR Trial (Study 307)/KEYNOTE-581 to be Presented at Upcoming Medical Meeting
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November 9, 2020
Sysmex Presents Academic Report with a View to Creating a Simple Method of Diagnosing Alzheimer’s Disease Using Blood
The Content Presented at the 13th Clinical Trials on Alzheimer’s Disease (CTAD) Conference
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November 7, 2020
Update on FDA Advisory Committee’s meeting on aducanumab in Alzheimer’s disease
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October 30, 2020
European Medicines Agency Accepts Biogen’s Aducanumab Marketing Authorization Application for Alzheimer's Disease
If approved, aducanumab would become the first therapy to reduce the clinical decline of Alzheimer’s disease and to meaningfully change the course of Alzheimer’s disease
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October 28, 2020
EISAI TO PRESENT LATEST DATA ON PIPELINE ASSETS IN THE AREA OF ALZHEIMER’S DISEASE AND DEMENTIA AT THE 13TH CLINICAL TRIALS ON ALZHEIMER’S DISEASE CONFERENCE
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October 27, 2020
EISAI AND JD HEALTH ESTABLISH A JOINT VENTURE COMPANY IN CHINA TO IMPLEMENT HEALTH SERVICE PLATFORM
Aiming to make a new contribution through a One-Stop Online Service for people living with Dementia in China
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October 27, 2020
GLOBAL COALITION FOR ADAPTIVE RESEARCH, AMGEN, AND EISAI ANNOUNCE FIRST PATIENT ENROLLED IN INTERNATIONAL COVID-19 TRIAL
AMGEN AND EISAI TO PARTICIPATE IN THE IMMUNE MODULATION DOMAIN OF REMAP-COVID, AN ADAPTIVE CLINICAL TRIAL TO TEST INTERVENTIONS FOR PATIENTS HOSPITALIZED WITH COVID-19
AMGEN’S APREMILAST AND EISAI’S ERITORAN TO BE EVALUATED ACROSS MULTIPLE INTERNATIONAL TRIAL SITES WITHIN THE REMAP NETWORK
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October 26, 2020
Eisai and Cogstate Expand Agreement for Global Development and Commercialization of Digital Cognitive Assessment Technologies
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October 21, 2020
NOTICE REGARDING BIOGEN’S DISCLOSURE ABOUT THE SUBMISSION OF MARKETING AUTHORIZATION APPLICATION TO EUROPEAN MEDICINES AGENCY FOR ADUCANUMAB FOR ALZHEIMER’S DISEASE
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October 16, 2020
SUPPLEMENTARY NEW DRUG APPLICATIONS FOR ANTI-EPILEPTIC DRUG FYCOMPA® AS MONOTHERAPY FOR PARTIAL-ONSET SEIZURES, PEDIATRIC INDICATION FOR PARTIAL-ONSET SEIZURES ACCEPTED IN CHINA
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October 8, 2020
THE UNIVERSITY OF TOKYO AND EISAI ANNOUNCE RESEARCH COLLABORATION FOR THE DEVELOPMENT AND DRUG DISCOVERY OF TARGETED PROTEIN DEGRADATION TECHNOLOGY
Establishment of Social Cooperation Program “Protein Degradation Drug Discovery”
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October 6, 2020
INDUSTRY-ACADEMIA-GOVERNMENT JOINT DEVELOPMENT AGREEMENT AIMING FOR DRUG DISCOVERY FOR COVID-19 UTILIZING ERITORAN AND E6011 CONCLUDED, NON-CLINICAL RESEARCH ACTIVITIES COMMENCE
Adopted for the public call for AMED "Development of therapeutic drugs for the novel coronavirus infection (COVID-19)"
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September 30, 2020
Eisai and Seikagaku Enter into Agreement for the Marketing Alliance of SI-613, a Treatment of Osteoarthritis, in South Korea
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September 25, 2020
JYSELECA® (FILGOTINIB) APPROVED IN JAPAN FOR RHEUMATOID ARTHRITIS
Filgotinib Demonstrates Durable Efficacy and Consistent Safety Profile Through 52 Weeks in Clinical Trials
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September 23, 2020
EISAI RECEIVES POSITIVE OPINION FROM EMA’S CHMP ON USE OF ANTIEPILEPTIC AGENT FYCOMPA® IN PEDIATRIC PATIENTS
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September 23, 2020
Eisai and Merck Present First-Time Data From Two Studies Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Seven Different Tumor Types at ESMO Virtual Congress 2020
New Results Include Findings From the Phase 2 LEAP-004 Trial Showing an ORR of 21.4% in Patients With Unresectable or Advanced Melanoma Who Had Previously Progressed on an Anti-PD-1/PD-L1 Therapy
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September 18, 2020
EISAI PRESENTS LATEST DATA OF PHASE I CLINICAL TRIAL ON LIPOSOMAL FORMULATION OF ANTI-CANCER AGENT HALAVEN® (ERIBULIN) AT ESMO VIRTUAL CONGRESS 2020
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September 17, 2020
EISAI ESTABLISHES PHARMA SALES SUBSIDIARY IN VIETNAM
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September 11, 2020
EISAI TO PRESENT ABSTRACTS ON ONCOLOGY PRODUCTS AND PIPELINE AT ESMO VIRTUAL CONGRESS 2020
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September 7, 2020
EISAI TO TAKE OVER MANUFACTURING AND MARKETING APPROVAL FOR EQUFINA® 50MG TABLETS (SAFINAMIDE MESILATE) IN JAPAN FROM MEIJI SEIKA PHARMA
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August 25, 2020
Relieving discomfort caused by dry skin with the moisturizing effect of pharmaceutical care products
EISAI TO LAUNCH SAHNE® MEDICAL SPRAY AND SAHNE® MEDICAL CREAM
Sahne Medical Spray is the first OTC drug spray-type lotion containing Heparinoid
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August 25, 2020
EISAI TO PRESENT LATEST DATA OF LEMBOREXANT AT 34th ANNUAL SLEEP MEETING (SLEEP2020)
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August 7, 2020
FDA Accepts Biogen’s Aducanumab Biologics License Application for Alzheimer's Disease with Priority Review
Priority Review accelerates FDA review time, with a Prescription Drug User Fee Act (PDUFA) target action on March 7, 2021
If approved, aducanumab would be the first treatment to meaningfully change the course of Alzheimer’s disease
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August 6, 2020
EISAI SUPPORTS RELIEF EFFORTS FOR THE HEAVY RAIN EVENT OF JULY 2020 IN JAPAN
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July 30, 2020
APPLICATION FOR ADDITIONAL INDICATION OF ANTI CANCER AGENT LENVIMA® FOR UNRESECTABLE THYMIC CARCINOMA SUBMITTED IN JAPAN
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July 28, 2020
EISAI AND DeNA TO PROVIDE SMARTPHONE APP “EASIIT APP” THROUGH BUSINESS ALLIANCE AGREEMENT
EISAI DEMENTIA PLATFORM EASIIT COMMENCES
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July 27, 2020
EISAI LISTED FOR 19TH CONSECUTIVE YEAR IN FTSE4GOOD INDEX SERIES, AN INDEX FOR SOCIALLY RESPONSIBLE INVESTMENT
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July 22, 2020
EISAI TO PRESENT LATEST DATA ON PIPELINE ASSETS IN THE AREA OF ALZHEIMER’S DISEASE AND DEMENTIA AT THE ALZHEIMER’S ASSOCIATION INTERNATIONAL CONFERENCE (AAIC) 2020
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July 20, 2020
Smartphone app for vital signs measurement of patients with the novel coronavirus infection
Experimental study project adopted as AMED project
Preventing medical infrastructure collapse by a monitoring system linked to LINE
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July 14, 2020
INITIATION OF NEW PHASE III CLINICAL STUDY (AHEAD 3-45) OF BAN2401 PRECLINICAL (ASYMPTOMATIC) ALZHEIMER’S DISEASE
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July 10, 2020
INDUSTRY-ACADEMIA-GOVERNMENT JOINT DEVELOPMENT AGREEMENT AIMING FOR DRUG DISCOVERY FOR SYSTEMIC LUPUS ERYTHEMATOSUS BY PRACTICAL APPLICATION OF TOLL-LIKE RECEPTOR RESEARCH CONCLUDED
RESEARCH ACTIVITIES COMMENCE
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July 8, 2020
Biogen Completes Submission of Biologics License Application to FDA for Aducanumab as a Treatment for Alzheimer’s Disease
If approved, aducanumab would be the first treatment with the potential to meaningfully change the course of Alzheimer’s disease
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July 8, 2020
Eisai and Merck Receive Complete Response Letter for LENVIMA® (lenvatinib) plus KEYTRUDA® (pembrolizumab) Combination as First-Line Treatment for Unresectable Hepatocellular Carcinoma
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July 8, 2020
EISAI SUBMITS MARKETING AUTHORIZATION APPLICATION IN JAPAN FOR ANTICANCER AGENT TAZEMETOSTAT FOR EZH2 GENE MUTATION-POSITIVE FOLLICULAR LYMPHOMA
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July 8, 2020
NEW DRUG APPLICATION FOR IN-HOUSE DEVELOPED NEW ANTI-INSOMNIA DRUG DAYVIGO® ACCEPTED IN HONG KONG
FIRST NEW DRUG APPLICATION FOR DAYVIGO IN ASIA OUTSIDE JAPAN
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July 6, 2020
EISAI TO LAUNCH IN-HOUSE DEVELOPED NEW ANTI-INSOMNIA DRUG DAYVIGO® (LEMBOREXANT) WITH INDICATION FOR INSOMNIA IN JAPAN
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July 6, 2020
NEW FINE GRANULE FORMULATION OF ANTI-EPILEPTIC DRUG FYCOMPA® LAUNCHED IN JAPAN
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July 1, 2020
REMAP-CAP TO PARTNER WITH EISAI ON INNOVATIVE TRIAL TO COMBAT COVID
GCAR, EISAI AND UPMC, ON BEHALF OF REMAP-CAP INVESTIGATOR NETWORK, ANNOUNCE ERITORAN’S INCLUSION IN REMAP-COVID, AN ADAPTIVE CLINICAL TRIAL TO TEST INTERVENTIONS FOR PATIENTS WITH MODERATE AND SEVERE COVID INFECTION
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EISAI’S ERITORAN SELECTED AS THE FIRST INVESTIGATIONAL IMMUNE MODULATION THERAPY TO BE EVALUATED ACROSS MULTIPLE INTERNATIONAL TRIAL SITES
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June 29, 2020
Position and Policy Regarding Reduction in the Trading Unit of the Company's Shares
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June 25, 2020
EISAI RECEIVES APPROVAL FOR PARKINSON’S DISEASE TREATMENT EQUFINA® IN SOUTH KOREA
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June 23, 2020
SHELF REGISTRATION FOR ISSUANCE OF STOCK OPTIONS
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June 19, 2020
CONTINUATION OF “POLICY FOR PROTECTION OF THE COMPANY’S CORPORATE VALUE AND COMMON INTERESTS OF SHAREHOLDERS (SHAREHOLDER RIGHTS PLAN)”
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June 10, 2020
EISAI TO SUPPORT COUNTER-MEASURES AGAINST THE SPREAD OF THE NOVEL CORONAVIRUS INFECTION IN AFRICA
SUPPORT FOR CONTINUATION OF ELIMINATION ACTIVITIES FOR NEGLECTED TROPICAL DISEASES AND SUPPORT FOR DEVELOPMENT AND POPULARIZATION OF MOBILE HEALTH PLATFORM
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June 4, 2020
BRAIN PERFORMANCE (BRAIN-HEALTH) SELF-CHECK TOOL “NOUKNOW™” TO BE USED IN BEAUTY SALONS
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June 2, 2020
EISAI LAUNCHES NEW INSOMNIA DRUG DAYVIGO™ (LEMBOREXANT) CIV IN THE UNITED STATES AS A TREATMENT OPTION FOR ADULTS WITH INSOMNIA
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May 29, 2020
AbbVie and Eisai Announce an approval for partial changes in the marketing approval of HUMIRA®, a Fully Human Anti-TNFα Monoclonal Antibody, concerning the dosage and administration related to the indication of hidradenitis suppurativa
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May 29, 2020
Results from LENVIMA® (lenvatinib) plus KEYTRUDA® (pembrolizumab) Trials in Unresectable Hepatocellular Carcinoma and Advanced Renal Cell Carcinoma to be Presented at 2020 ASCO Annual Meeting
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May 18, 2020
The effect of SEI-I* evokes the joy of eating
EISAI TO LAUNCH NEW SELBELLE® PREMIUM TABLETS AND NEW SELBELLE® PREMIUM FINE GRANULES
The first OTC product containing the same amount of stomach-protecting teprenone as for medical purposes
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May 14, 2020
EISAI TO PRESENT DATA ON ONCOLOGY PIPELINE AND PRODUCTS AT ASCO ANNUAL MEETING
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April 27, 2020
EISAI SELECTED AS MOST HONORED COMPANY AND THE FIRST PLACE OF THE SECTOR IN “THE ALL-JAPAN EXECUTIVE TEAM (BEST IR COMPANY RANKING)” BY INSTITUTIONAL INVESTOR MAGAZINE
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April 1, 2020
Eisai and Seikagaku Enter into Agreement for the Co-development and Marketing Alliance of SI-613, a Treatment of Osteoarthritis, in China
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March 26, 2020
EISAI SUBMITS MARKETING AUTHORIZATION APPLICATION IN JAPAN FOR ANTICANCER AGENT DENILEUKIN DIFTITOX (GENETIC RECOMBINANT) FOR CUTANEOUS T-CELL LYMPHOMA AND PERIPHERAL T-CELL LYMPHOMA
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March 25, 2020
DISCOVERY RESEARCH ON MULTIKINASE INHIBITOR LENVATINIB HONORED WITH PSJ AWARD FOR DRUG RESEARCH AND DEVELOPMENT ’20
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March 23, 2020
EISAI TO LAUNCH DIGITAL TOOL “NOUKNOW™” IN JAPAN FOR REGULAR SELF-ASSESSMENT OF BRAIN PERFORMANCE (BRAIN HEALTH)
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March 19, 2020
All-case Surveillance Condition for Approval of “Actonel® 17.5 mg tablets” for Treatment of Paget’s Disease of Bone Cleared in Japan
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February 25, 2020
Eisai and FUJI YAKUHIN Conclude License Agreement Concerning the Development and Distribution of Dotinurad, a Treatment for Hyperuricemia and Gout, in China
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February 21, 2020
EISAI RECEIVES THE PRESIDENT’S AWARD OF THE JAPAN TECHNO-ECONOMICS SOCIETY AT THE 8TH TECHNOLOGY MANAGEMENT AND INNOVATION AWARDS
FOR ITS CONTRIBUTIONS TOWARDS PATIENTS WITH LIVER DISEASE THROUGH THE EISAI-ORIGINATED ORALLY AVAILABLE KINASE INHIBITOR LENVIMA®
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January 30, 2020
EISAI TO SUPPORT COUNTER MEASURES FOR CHINA’S NOVEL CORONAVIRUS-ASSOCIATED PNEUMONIA SPREAD IN CHINA
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January 29, 2020
EISAI COMMENCES JOINT RESEARCH AND DEVELOPMENT OF CANCER GENE PANEL TEST WITH PERSONAL GENOME DIAGNOSTICS INC. USING LIQUID BIOPSY TO ACCELERATE NEXT-GENERATION DRUG DISCOVERY AND DEVELOPMENT
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January 23, 2020
DAYVIGO™ (LEMBOREXANT) APPROVED FOR TREATMENT OF INSOMNIA IN JAPAN
NON-SEDATIVE OREXIN RECEPTOR ANTAGONIST DEMONSTRATES EFFECTIVENESS FOR BOTH SLEEP ONSET AND SLEEP MAINTENANCE
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January 23, 2020
APPROVAL OF ANTIEPILEPTIC DRUG FYCOMPA® IN JAPAN FOR MONOTHERAPY AND PEDIATRIC INDICATIONS FOR PARTIAL-ONSET SEIZURES, AS WELL AS A NEW FORMULATION
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January 20, 2020
Eisai Rated “A”, the highest rating in the CDP Climate Change Report 2019
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January 10, 2020
LAUNCH OF ANTICANCER AGENT HALAVEN® IN CHINA
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January 6, 2020
FYCOMPA® FOR ADJUNCTIVE TREATMENT OF PARTIAL ONSET SEIZURES LAUNCHED IN CHINA