Takeda Pharmaceutical Gestione

Criteri Gestione verificati 2/4

Al momento non disponiamo di informazioni sufficienti sull'amministratore delegato.

Informazioni chiave

Julie Kim

Amministratore delegato

n/a

Compenso totale

Percentuale dello stipendio del CEO	n/a
Mandato del CEO	no data
Proprietà del CEO	0.005%
Durata media del management	3.3yrs
Durata media del Consiglio di amministrazione	3yrs

Aggiornamenti recenti sulla gestione

Recent updates

AMMINISTRATORE DELEGATO

Julie Kim (56 yo)

no data

Mandato

Ms. So-Young Kim, also known as Julie, is CEO, President & Director of Takeda Pharmaceutical Company Limited from June 24, 2026. She joined the Takeda Pharmaceutical Company Limited in January 2019. She wa...

Gruppo dirigente

Nome	Posizione	Mandato	Compensazione	Proprietà
Milano Furuta	CFO & Director	2.2yrs	JP¥384.00m	0.0019% € 851.0k
Andrew S. Plump	President of Research & Development and Representative Director	no data	JP¥1.26b	0.020% € 8.7m
So-Young Kim	CEO, President & Director	no data	Nessun dato	0.0055% € 2.4m
Seigo Izumo	Chair of Management Board	no data	Nessun dato	Nessun dato
Haruhiko Hirate	Member of Management Board	no data	Nessun dato	Nessun dato
Salvatore Alesci	Member of Management Board and Head of R&D Global Science & Biomedical Policy	no data	Nessun dato	Nessun dato
Michael Fox	Chief Operating Officer	no data	Nessun dato	Nessun dato
Norimasa Takeda	Chief Accounting Officer & Corporate Controller	no data	Nessun dato	Nessun dato
Iwaaki Taniguchi	Senior Vice President of Corporate Finance & Controlling Department	13.3yrs	Nessun dato	Nessun dato
Gabriele Ricci	Chief Data & Technology Officer	4.3yrs	Nessun dato	0.0025% € 1.1m
Christopher David O'Reilly	Global Head of Investor Relations & Global Finance	5.8yrs	Nessun dato	Nessun dato
Natalie Furney	Global General Counsel	1.2yrs	Nessun dato	Nessun dato

3.3yrs

Durata media

51yo

Età media

Gestione esperta: Il team dirigenziale di TKDA è considerato esperto (durata media dell'incarico 3.3 anni).

Membri del Consiglio di amministrazione

Nome	Posizione	Mandato	Compensazione	Proprietà
Milano Furuta	CFO & Director	2yrs	JP¥384.00m	0.0019% € 851.0k
Andrew S. Plump	President of Research & Development and Representative Director	11yrs	JP¥1.26b	0.020% € 8.7m
So-Young Kim	CEO, President & Director	no data	Nessun dato	0.0055% € 2.4m
John Michael Maraganore	Independent External Director	4yrs	JP¥44.00m	0.00024% € 105.3k
Steven S. Gillis	Independent External Director	7.4yrs	JP¥53.00m	0.00050% € 219.3k
Paulus Stoffels	Independent External Director	no data	Nessun dato	Nessun dato
Bruce Broussard	Independent External Director	no data	Nessun dato	0.000030% € 13.2k
Miki Tsusaka	Independent External Director	3yrs	JP¥38.00m	Nessun dato
Masami Iijima	Independent External Chair	5yrs	JP¥43.00m	0.00041% € 179.9k
Kimberly A. Reed	Independent External Director	4yrs	JP¥47.00m	0.00028% € 122.8k
Koichiro Kimura	Independent External Director	no data	Nessun dato	Nessun dato

3.0yrs

Durata media

63yo

Età media

Consiglio di amministrazione esperto: I membri del consiglio di amministrazione di TKDA sono considerati esperti (durata media dell'incarico 3 anni).

Analisi aziendale e situazione dei dati finanziari

Dati	Ultimo aggiornamento (ora UTC)
Analisi dell'azienda	2026/06/30 23:18
Prezzo dell'azione a fine giornata	2026/06/30 00:00
Utili	2026/03/31
Utili annuali	2026/03/31

Fonti dei dati

I dati utilizzati nella nostra analisi aziendale provengono da S&P Global Market Intelligence LLC. I seguenti dati sono utilizzati nel nostro modello di analisi per generare questo report. I dati sono normalizzati, il che può comportare un ritardo nella disponibilità della fonte.

Pacchetto	Dati	Tempistica	Esempio Fonte USA ^*
Dati finanziari della società	10 anni	Conto economico Rendiconto finanziario Bilancio	Modulo SEC 10-K Modulo SEC 10-Q
Stime di consenso degli analisti	+3 anni	Previsioni finanziarie Obiettivi di prezzo degli analisti	Rapporti di ricerca degli analisti Blue Matrix
Prezzi di mercato	30 anni	Prezzi delle azioni Dividendi, scissioni e azioni	Dati di mercato ICE Modulo SEC S-1
Proprietà	10 anni	Top azionisti Insider trading	Modulo 4 SEC Modulo 13D SEC
Gestione	10 anni	Team di leadership Consiglio di amministrazione	Modulo SEC 10-K Modulo SEC DEF 14A
Sviluppi principali	10 anni	Annunci aziendali	Modulo 8-K SEC

* Esempio per i titoli statunitensi, per i titoli non statunitensi si utilizzano forme e fonti normative equivalenti.

Se non specificato, tutti i dati finanziari si basano su un periodo annuale ma vengono aggiornati trimestralmente. Si tratta dei cosiddetti dati TTM (Trailing Twelve Month) o LTM (Last Twelve Month). Per saperne di più.

Modello di analisi e Snowflake

I dettagli del modello di analisi utilizzato per generare questo report sono disponibili sulla nostra pagina Github; disponiamo inoltre di guide su come utilizzare i nostri report e di tutorial su Youtube.

Scoprite il team di livello mondiale che ha progettato e realizzato il modello di analisi Simply Wall St.

Metriche di settore e industriali

Le nostre metriche di settore e di sezione sono calcolate ogni 6 ore da Simply Wall St; i dettagli del nostro processo sono disponibili su Github.

Fonti analitiche

Takeda Pharmaceutical Company Limited è coperta da 27 analisti. 15 di questi analisti ha fornito le stime di fatturato o di utile utilizzate come input per il nostro report. Le stime degli analisti vengono aggiornate nel corso della giornata.

Analista	Istituzione
Atsushi Seki	Barclays
Miki Sogi	Bernstein
Koichi Mamegano	BofA Global Research

Takeda Pharmaceutical Gestione

Criteri Gestione verificati 2/4

Informazioni chiave

Aggiornamenti recenti sulla gestione

Takeda Pharmaceutical Company Limited Announces Management and Committee Changes

Takeda Pharmaceutical Company Limited, Annual General Meeting, Jun 24, 2026

Takeda Pharmaceutical Company Limited Announces Board and Executive Retirements

Takeda Announces Executive Changes, Effective June 2026

Takeda Pharmaceutical Company Limited Announces Change in Compensation Committee Members, Effective June 25, 2025

Takeda Pharmaceutical Company Limited, Annual General Meeting, Jun 25, 2025

Recent updates

Takeda Pharmaceutical Company Limited Announces Management and Committee Changes

Takeda Pharmaceutical Company Limited Presents Additional Results from Two Pivotal Studies Showing Oveporexton Improves Daily Function, Cognition, and Nighttime Sleep for People with Narcolepsy Type 1

Takeda Announces Positive Topline Results for Phase 3 Study Comparing Zasocitinib to Deucravacitinib in Adults with Moderate-To-Severe Plaque Psoriasis

Takeda Pharmaceutical Company Limited to Report Q2, 2027 Results on Oct 29, 2026

Takeda Pharmaceutical Company Limited, Annual General Meeting, Jun 24, 2026

Takeda Pharmaceutical Company Limited Announces Positive Topline Results From Pivotal Phase 2/3 Clinical Trial Of TAK-881 In Primary Immunodeficiency Disease

Takeda Pharmaceutical Company Limited Announces Zasocitinib Delivers Rapid and Durable Skin Clearance in Plaque Psoriasis

Takeda Pharmaceutical Company Limited Announces Board and Executive Retirements

Takeda Pharmaceuticals USA, Inc., Takeda Pharmaceutical Company Limited and Eli Lilly and Company Announce National Third-Party Payor Class Certified in Lawsuit Regarding Actos

Takeda Pharmaceutical Company Limited to Report Q1, 2027 Results on Jul 30, 2026

Takeda and Protagonist Therapeutics, Inc Announce FDA Accepts Priority Review for First-In-Class Therapy Rusfertide in Polycythemia Vera

Takeda Announces Positive Phase 3 Data Demonstrate Potential for ENTYVIO®? (vedolizumab) to Address Treatment Gap for Children and Adolescents with Moderate to Severe Ulcerative Colitis

U.S. Food and Drug Administration Accepts New Drug Application and Grants Priority Review for Takeda Pharmaceutical Company Limited's Oveporexton (TAK-861) as A Potential First-In-Class Therapy for Narcolepsy Type 1

Takeda Pharmaceutical Company Limited Revises Consolidated Earnings Guidance for the Fiscal Year 2025

Takeda Announces U.S. Availability of GAMMAGARD LIQUID ERC, the Only Ready-To-Use Liquid Immunoglobulin Therapy with Low Immunoglobulin A (IgA) Content

Takeda and Protagonist Announce Submission of New Drug Application for Rusfertide for Treatment of Polycythemia Vera

Takeda’s Zasocitinib Landmark Phase 3 Plaque Psoriasis Data Show Promise to Deliver Clear Skin in a Once-Daily Pill, Catalyzing a New Era of Treatment

Takeda Pharmaceutical Company Limited to Report Q3, 2026 Results on Jan 29, 2026

Protagonist Therapeutics, Inc. and Takeda Pharmaceutical Company Limited Present Longer-Term Data At ASH 2025 Showing Rusfertide Delivers Durable Response and Hematocrit Control in Polycythemia Vera

Wisner Baum Unleashes Rico Against Takeda Pharmaceuticals and Eli Lilly

Takeda Presents New Data Showing Mezagitamab Sustained Effect on Kidney Function 18 Months After Treatment in Primary IgA Nephropathy

Takeda Inc. Announces Completion of the 7-Year Pivotal Phase 3 Tides Trial Evaluating Its Dengue Vaccine, Qdenga®?V

Takeda Pharmaceutical Company Limited Declares Dividend for Second Quarter-End of Fiscal Year Ending March 31, 2026, Payable on December 1, 2025

Takeda Inc. Announces the Recently FDA- Approved Hyhub and Hyhub Duo Devices Now Available in the U.S. to Simplify Hyqvia® Infusion Preparation

Takeda Announces Executive Changes, Effective June 2026

Takeda Presents Orexin Data from Landmark Oveporexton Phase 3 Program in Narcolepsy Type 1 at World Sleep 2025

Takeda Announces U.S. FDA Approves Expanded Indication for VONVENDI for Adults and Children with Von Willebrand Disease

Takeda Pharmaceutical Company Limited to Report Q2, 2026 Results on Oct 30, 2025

Takeda Pharmaceutical Company Limited Announces an Embargoed Version of an Abstract for Phase 3 TAK-861-3002 Study (Radiantlight) of Oveporexton (TAK-861) in Narcolepsy Type 1, Which Is Slated to Be Presented At the Upcoming World Sleep 2025 Congress

Takeda Pharmaceutical Company Limited Reaffirms Earnings Guidance for the Fiscal Year 2025

Takeda Receives FDA 510(k) Clearance for HyHubTM and HyHub Duo Devices to Simplify HYQVIA Administration

Takeda Announces Positive Results from Two Pivotal Phase 3 Studies of Oveporexton (Tak-861) in Narcolepsy Type 1

Takeda Pharmaceutical Company Limited Approves Dividend

Takeda Pharmaceutical Company Limited Announces U.S. FDA Approval of Gammard Liquid Immunoglobulin Therapy with Low Immunoglobulin A (IgA) Content

Takeda Pharmaceutical Company Limited Announces Change in Compensation Committee Members, Effective June 25, 2025

Ninth Circuit Affirms Actos RICO Class Action Certification Against Takeda and Eli Lilly

European Commission Approves Adcetris®? (Brentuximab Vedotin) for the Treatment of Adult Patients with Newly Diagnosed Stage Iib/Iii/Iv Hodgkin Lymphoma in Combination with Ecadd

Protagonist Therapeutics, Inc. and Takeda Announce Asco Plenary Presentation Highlighting Full 32-Week Results from Phase 3 Verify Study of Rusfertide

Takeda Announces The New England Journal of Medicine Publishes Data from Phase 2b Trial of Oral Orexin Receptor 2 Agonist Oveporexton (TAK-861) in People with Narcolepsy Type 1

Takeda Pharmaceutical Company Limited, Annual General Meeting, Jun 25, 2025

Takeda Pharmaceutical Company Limited Receives Approval by the Japanese Ministry of Health, Labour, and Welfare for Livmarli®? (Maralixibat) Oral Solution for the Treatment of Alagille Syndrome and Progressive Familial Intrahepatic Cholestasis in Japan

Protagonist Therapeutics, Inc. and Takeda Pharmaceutical Company Limited Announces Positive Topline Results from Phase 3 Verify Study of Rusfertide in Patients with Polycythemia Vera

Takeda Pharmaceutical Company Limited to Report Q1, 2026 Results on Jul 30, 2025

Takeda Pharmaceutical Company Limited (TSE:4502) announces an Equity Buyback for 28,500,000 shares, representing 1.8% for ¥100,000 million.

Takeda Announces Approval of HYQVIA® 10% S.C. (Subcutaneous) Injection Set in Japan for Patients with Agammaglobulinemia or Hypogammaglobulinemia

Takeda Pharmaceutical Company Limited to Report Q3, 2025 Results on Jan 30, 2025

Takeda Pharmaceutical Company Limited Raises Earnings Guidance for the Full Year 2024

Takeda Receives Approval from the Japanese Ministry of Health, Labour and Welfare to Manufacture and Market Fruquintinib for Previously Treated Colorectal Cancer

Takeda Receives European Commission Approval for ADZYNMA®

Corza Medical Inc. completed the acquisition of TachoSil manufacturing operations in Linz, Austria. from Takeda Pharmaceutical Company Limited (TSE:4502).

Takeda Receives European Commission Approval for FRUZAQLA® (fruquintinib)

Takeda Receives Approval from European Commission for Fruquintinib in Previously Treated Metastatic Colorectal Cancer

Takeda Announces Data from Phase 3 ADVANCE-CIDP 3 Clinical Trial of HYQVIA in Patients with Chronic Inflammatory Demyelinating Polyneuropathy at PNS Annual Meeting

Takeda Announces Phase 3 Topline Results for Soticlestat in Patients with Dravet Syndrome and Lennox-Gastaut Syndrome

Takeda Receives Positive CHMP Opinion for Recombinant ADAMTS13 (rADAMTS13) in Congenital Thrombotic Thrombocytopenic Purpura (cTTP)

Takeda Pharmaceutical Company Limited Announces Demise of its Board Member, Olivier Bohuon

Takeda Receives Positive Chmp Opinion for Fruquintinib in Previously Treated Metastatic Colorectal Cancer

U.S. Food and Drug Administration Approves Subcutaneous Administration of Takeda Pharmaceutical Company Limited's ENTYVIO (Vedolizumab) for Maintenance Therapy in Moderately to Severely Active Crohn's Disease

Alinamin Pharmaceutical Co., Ltd. acquired Nihon Pharmaceutical Co., Ltd. from Takeda Pharmaceutical Company Limited (TSE:4502).

Takeda Pharmaceutical Company Limited, Annual General Meeting, Jun 26, 2024

Takeda Pharmaceuticals U.S.A, Inc. Announces Approval of Adzynma Intravenous Injection 1500 (Apadamtase Alfa) in Japan for Patients with Congenital Thrombotic Thrombocytopenic Purpura

Takeda Announces U.S. FDA Approval of Supplemental New Drug Application for ICLUSIG® (ponatinib) in Adult Patients with Newly Diagnosed Ph+ ALL

Takeda Announces Positive Topline Results from Phase 2 Study Evaluating Mezagitamab (Tak-079), A Potential Best-In-Class Anti-Cd38 Monoclonal Antibody, for Primary Immune Thrombocytopenia

FDA Approves Takeda's EOHILIA (budesonide Oral Suspension)

Takeda Intends to Rapidly Initiate the First Global Phase 3 Trials of TAK-861, an Oral Orexin Agonist, in Narcolepsy Type 1 in First Half of Fiscal Year 2024

Takeda Pharmaceutical Company Limited Reaffirms Earnings Guidance for the Full Year of Fiscal 2024

Takeda Pharmaceutical Company Limited Announces Chief Financial Officer Succession, Effective April 1, 2024

Takeda's Gammard Liquidid®? Approves by U.S. Fda for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (Cidp)

Takeda Announces U.S. Food and Drug Administration Approves Hyqvia® [Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronidase]