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Eisai Bilanço Sağlığı

Finansal Sağlık kriter kontrolleri 5/6

Anahtar bilgiler

11.2%

Borç/özkaynak oranı

JP¥94.91b

Borç

Faiz karşılama oranı	n/a
Nakit	JP¥265.53b
Eşitlik	JP¥850.70b
Toplam yükümlülükler	JP¥410.57b
Toplam varlıklar	JP¥1.26t

Son finansal sağlık güncellemeleri

Güncelleme yok

Recent updates

Finansal Durum Analizi

Kısa Vadeli Yükümlülükler: ESAL.Y's short term assets (¥585.4B) exceed its short term liabilities (¥266.5B).

Uzun Vadeli Yükümlülükler: ESAL.Y's short term assets (¥585.4B) exceed its long term liabilities (¥144.0B).

Borç-Özkaynak Tarihçesi ve Analizi

Borç Seviyesi: ESAL.Y has more cash than its total debt.

Borcun Azaltılması: ESAL.Y's debt to equity ratio has reduced from 36% to 11.2% over the past 5 years.

Borç Kapsamı: ESAL.Y's debt is well covered by operating cash flow (32%).

Faiz Kapsamı: Insufficient data to determine if ESAL.Y's interest payments on its debt are well covered by EBIT.

This company listing is no longer active

Eisai Bilanço Sağlığı

Finansal Sağlık kriter kontrolleri 5/6

Anahtar bilgiler

Son finansal sağlık güncellemeleri

Recent updates

Eisai Co., Ltd. and Biogen Inc. Announce Lecanemab Receives Priority Review Status in Japan

Eisai Accepts Marketing Authorization Application for Lecanemab as Treatment for Early Alzheimer's Disease

Eisai Co., Ltd. Files Marketing Authorization Application for Anti-Amyloid-Beta Protofibril Antibody Lecanemab for Early Alzheimer's Disease in Japan

Eisai Co., Ltd. and Biogen Inc. Submits Marketing Authorization Application for Lecanemab as Treatment for Early Alzheimer's Disease in Europe

Eisai Co., Ltd. and Biogen Inc. Announce FDA Approves LEQEMBI (lecanemab-irmb) Under the Accelerated Approval Pathway for the Treatment of Alzheimer's Disease

Eisai Initiates BLA Submission of Data for Lecanemab in China

Eisai Presents Results of Lecanemab Phase 3 Confirmatory Clarity AD Study for Early Alzheimer's Disease at CTAD Conference

Eisai to Present Latest Data on Fycompa (Perampanel) CIII at the 76th American Epilepsy Society (AES) Annual Meeting

DKSH Holding AG (SWX:DKSH) signed an agreement to acquire Two pharma brands of Eisai.

Eisai Co., Ltd. Provides Consolidated Earnings Guidance for the Fiscal Year Ending March 31, 2023

Eisai Announces Real-World Evidence on the Clinical Effectiveness of LENVIMA® (lenvatinib) Monotherapy for the Treatment of Patients with Radioiodine-Refractory Differentiated Thyroid Cancer

Eisai Co. and Biogen Announce Positive Topline Results from Eisai's Large Global Phase 3 Confirmatory Clarity AD Clinical Trial of Lecanemab

Merck and Eisai Present Results From Phase 3 LEAP-002 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Versus LENVIMA Monotherapy in Patients With Unresectable Hepatocellular Carcinoma

Eisai Presents New Data from Its Oncology Portfolio and Pipeline At ESMO Congress 2022

Eisai Presents New Data for Lecanemab (Ban2401) At Alzheimer's Association International Conference

Merck & Co., Inc. and Eisai Co., Ltd. Provides Update on Phase 3 LEAP-002 Trial

Eisai Co., Ltd. and Biogen Inc. Announces U.S. Food and Drug Administration Accepted the Biologics License Application

Global Coalition for Adaptive Research Announces the Discontinued Evaluation of Eritoran in REMAP-COVID

Eisai Co., Ltd., Annual General Meeting, Jun 17, 2022

Eisai Co., Ltd., Annual General Meeting, Jun 17, 2022

Eisai Completes Rolling Submission to the U.S. FDA for Biologics License Application of Lecanemab for Early Alzheimer's Disease Under the Accelerated Approval Pathway

Eisai Co., Ltd. Announces Article About Long-Term Health Outcomes of Its Investigational Anti-Amyloid-Beta Protofibril Antibody Lecanemab in People Living

Eisai Co., Ltd. to Report Q2, 2023 Results on Nov 07, 2022

Eisai Co., Ltd. (TSE:4523) acquired an unknown minority stake in Arteryex Co., Ltd.

Eisai Co., Ltd. and Biogen Inc. Initiate A Submission to the Pharmaceuticals and Medical Devices Agency of Application Data Under the Prior Assessment Consultation System in Japan for the Investigational Anti-Amyloid Beta Protofibril Antibody Lecanemab

Eisai Co., Ltd. Provides Consolidated Earnings Guidance for the Fiscal Year Ending March 31, 2022

Biogen Inc. and Eisai Co., Ltd. Provides Update on the Phase 4 ENVISION Confirmatory Study of ADUHELM

Eisai Co., Ltd. Announces Dominantly Inherited Alzheimer Network Trials Unit Enrolls the First Subject in the Phase II/III Study

Biogen Inc. and Eisai Company, Ltd. Announces Japan’S Ndc of the Pharmaceutical Affairs and Food Sanitation Council Seeks Additional Data; Aducanumab Remains Under Review

Biogen Inc. and Eisai Co., Ltd. Announces Update on Regulatory Submission for Aducanumab in the European Union

Eisai Presents Final Results of Phase IV Elevate Study of Anti-Epileptic Drug FYCOMPA® (perampanel) at the American Epilepsy Society 2021 Annual Meeting

Eisai Co., Ltd. to Present Real-World Evidence And Convulsive Seizure Freedom Data Evaluating FYCOMPA® (perampanel) Across Patient Types At 75th American Epilepsy Society (AES) Annual Meeting

Eisai Initiates Rolling Submission To The U.S. FDA For Biologics License Application Of Lecanemab (BAN2401) For Early Alzheimer's Disease Under The Accelerated Approval Pathway

BioArctic AB's partner Eisai Initiates Rolling Submission for the US FDA Biologics License Application of Lecanemab for Early Alzheimer’s Disease Under the Accelerated Approval Pathway

Eisai Co., Ltd. Revises Earnings Guidance for the Fiscal Year Ending March 31, 2022

Eisai Co., Ltd. Announces That It Has Obtained Manufacturing and Marketing Approval for the Ezh2 Inhibitor "Tazverik® Tablets 200 Mg" with the Indication of Relapsed or Refractory Ezh2 Gene Mutation-Positive Follicular Lymphoma

Biogen and Eisai, Co., Ltd. Announces FDA Approval for Aduhelm as the First and Only Alzheimer’S Disease Treatment to Address A Defining Pathology of the Disease

Eisai Announces Real-World Data on the Effectiveness of HALAVEN® (eribulin mesylate) for the Treatment of Patients with Metastatic Breast Cancer (mBC) Published in Advances in Therapy

Eisai Co., Ltd. Announces Dividend for the Year Ended March 31, 2021, Payable on May 21, 2021; Provides Dividend Guidance for the Year Ending March 31, 2022

Merck and Eisai Receive Priority Review from FDA for Keytruda (Pembrolizumab) Plus Lenvima (Lenvatinib) Applications for Advanced Renal Cell Carcinoma and for Advanced Endometrial Carcinoma

Eisai Co., Ltd. to Report Q3, 2022 Results on Feb 03, 2022

Bioarctic and Eisai Present Latest Data Regarding Lecanemab at AD/PD 2021

Bioarctic AB (Publ) and Eisai to Present Data Relating to Its Investigational Anti-Amyloid Beta (Aß) Protofibril Antibody Lecanemab (BAN2401)

Eisai Co., Ltd. Revises Consolidated Earnings Guidance for the Full Year Ending March 31, 2021

Biogen and Eisai Announce FDA’s 3-Month Extension of Review Period for the Biologics License Application for Aducanumab

Eisai Co., Ltd. to Present Abstracts on Lenvatinib at 2021 Gastrointestinal Cancers Symposium

Biogen and Eisai, Co., Ltd. Files New Drug Application for Aducanumab in Japan

Eisai Co., Ltd. Announces Presentations on A Series of Abstracts Highlighting Updates on Its In-House Discovered Lenvatinib Mesylate Lenvima

Eisai Co., Ltd. and Wren Therapeutics Ltd. Enter into Research Collaboration Agreement for Drug Discovery for Synucleinopathies

Eisai Announces New Investigational Data from Study 211 Evaluating the Starting Dose of Lenvima

BioArctic AB (publ) Partner Eisai Presents Latest Data Regarding Drug Candidate BAN2401 at CTAD 2020

Eisai Announces Investigational Data Highlighting Lenvima® (Lenvatinib) Based Combination Therapy in Patients with Renal Cell Carcinoma At IKCS 2020

European Medicines Agency Accepts Biogen’s Aducanumab Marketing Authorization Application for Alzheimer's Disease

Global Coalition for Adaptive Research, Amgen, and Eisai Announce First Patient Enrolled in International Covid-19 Trial

Eisai and Seikagaku Enter into Agreement for the Marketing Alliance of SI-613, A Treatment of Osteoarthritis, in South Korea

Merck and Eisai Present First-Time Data from Two Studies Evaluating Keytruda® (Pembrolizumab) Plus Lenvima® (Lenvatinib) in Seven Different Tumor Types at ESMO Virtual Congress 2020

Eisai Co., Ltd. Announces the Latest Results from the Cohort Targeting Patients with HER2-Negative Breast Cancer in the Phase I Clinical Trial for the New Liposomal Formulation (E7389-LF)

Finansal Durum Analizi

Borç-Özkaynak Tarihçesi ve Analizi

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