Takeda Pharmaceutical Company Limited (VIE:TKD)

Austria flag Austria · Delayed Price · Currency is EUR
27.69
+0.29 (1.06%)
Last updated: Jun 26, 2026, 11:00 AM CET
Market Cap43.59B +5.9%
Revenue (ttm)24.58B -1.7%
Net Income-831.22M
EPS-0.53
Shares Out n/a
PE Ration/a
Forward PEn/a
Dividend1.11 (4.04%)
Ex-Dividend DateMar 30, 2026
Volumen/a
Open27.71
Previous Close27.40
Day's Range27.69 - 27.71
52-Week Range22.83 - 32.16
Betan/a
Analystsn/a
Price Targetn/a
Earnings DateJul 30, 2026

About VIE:TKD

Takeda Pharmaceutical Company Limited engages in the research, development, manufacture, marketing, and out-licensing of pharmaceutical products. It offers pharmaceutical products in the areas of gastroenterology, rare diseases, plasma-derived therapies, oncology, vaccines, and neuroscience. The company provides its products under the Entyvio, Gattex/Revestive, Takecab/Vocinti, EOHILIA, Takhzyro, Advate, Elaprase, Replagal, Vpriv, Adynovate/Adynovi, Livtencity, ADZYNMA, Gammagard Liquid/Kiovig, Hyqvia, Cuvitru, Flexbumin, Adcetris, Leuplin/Enan... [Read more]

Industry Pharmaceutical Preparations
Founded 1781
Employees 47,029
Stock Exchange Vienna Stock Exchange
Ticker Symbol TKD

Financial Performance

Financial numbers in JPY Financial Statements

News

Takeda Announces New Assignments of Directors and Appointment of Julie Kim as Representative Director, President and CEO

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--In the final step of its 18-month CEO transition, Takeda (TOKYO:4502/NYSE:TAK) today announced that Julie Kim was officially appointed Takeda's Repres...

2 days ago - Business Wire

New Pivotal Study Data Show Takeda's Oveporexton Improved Daily Function, Cognition and Nighttime Sleep for People with Narcolepsy Type 1

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) today presented additional results from two pivotal studies at SLEEP 2026, showing oveporexton (TAK-861), an oral orexin re...

11 days ago - Business Wire

Takeda's AI-crafted psoriasis pill tops Bristol Myers' Sotyktu in head-to-head trial

Japan's Takeda Pharmaceutical said on Thursday its experimental once-daily psoriasis pill, developed with the help of AI, outperformed Bristol Myers Squibb's approved ​drug Sotyktu in a late-stage hea...

15 days ago - Reuters

Takeda's Zasocitinib Significantly Outperforms Deucravacitinib in Head-to-Head Phase 3 Psoriasis Study, Promising to Redefine Oral Treatment Expectations

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) announced positive topline results for the Phase 3, randomized, multicenter, double-blind study comparing zasocitinib (TAK-...

15 days ago - Business Wire

U.S. FDA Accepts Takeda's Application for Intravenous ENTYVIO® (vedolizumab) in Pediatric Ulcerative Colitis and Crohn's Disease

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) today announced the U.S. Food and Drug Administration (FDA) has accepted for review its supplemental Biologics License Appl...

17 days ago - Business Wire

Takeda Pharmaceutical Company Transcript: Jefferies Global Healthcare Conference 2026

Leadership transition is underway with Julie Kim as CEO, supported by a refreshed executive team and board. Three major product launches are expected to drive growth, while a transformation plan aims for significant cost savings and improved margins. ENTYVIO and plasma-derived therapies remain key revenue drivers amid evolving market dynamics.

23 days ago - Transcripts

Takeda engaged in antitrust scheme to delay generic constipation drug, US jury finds

A ​U.S. jury on ‌Monday found that ​Takeda ​Pharmaceutical caused pharmacies, ⁠insurers, ​retailers and ​others to sustain about $885 million ​in ​damages delaying the ‌release ⁠of a generic version o...

5 weeks ago - Reuters

Takeda to cut about 4,500 jobs in fiscal 2026 as it steps up restructuring

Japan's Takeda Pharmaceutical , plans to cut about 4,500 jobs in fiscal year 2026, as it pushes ahead with ​a restructuring to centralize corporate functions and reduce ‌costs.

6 weeks ago - Reuters

Takeda Pharmaceutical Company Earnings Call Transcript: Q4 2026

FY 2025 saw resilient financials despite VYVANSE erosion, with core revenue at JPY 4.5T and strong pipeline progress. Three late-stage assets are set for launch, supporting a new growth phase, while cost discipline and transformation programs underpin future margin expansion and capital flexibility.

6 weeks ago - Transcripts

Takeda Pharmaceutical Company Slides: Q4 2026

Takeda Pharmaceutical Company has posted slides in relation to its Q4 2026 quarterly earnings report, which was published on May 13, 2026.

6 weeks ago - Filings

Takeda Pharmaceutical Company Quarterly report: Q4 2026

Takeda Pharmaceutical Company has published its Q4 2026 quarterly earnings report on May 13, 2026.

6 weeks ago - Filings

Takeda Pharmaceutical Company Annual report: Q4 2026

Takeda Pharmaceutical Company has published its Q4 2026 annual report on May 13, 2026.

6 weeks ago - Filings

Takeda Announces FY2025 Full Year Results and FY2026 Outlook, Highlighted by Excellent Pipeline Progress and Solid FY2025 Results

OSAKA, Japan--(BUSINESS WIRE)--Takeda (TOKYO:4502/NYSE:TAK) today announced financial results for the fiscal year 2025 (period ended March 31, 2026). The Company delivered solid results in line with i...

6 weeks ago - Business Wire

Takeda's immune disease drug meets main goal of mid-to-late stage trial

Takeda Pharmaceutical ​said its ‌experimental drug ​for ​primary immunodeficiency disease, ⁠a ​rare condition ​that weakens the ​immune ​system, has met ‌the ⁠main goal of a ​mid- ​to ⁠late-stage ​cli...

7 weeks ago - Reuters

Takeda Announces Positive Topline Results from Pivotal Phase 2/3 Clinical Trial of TAK-881 in Primary Immunodeficiency Disease (PID)

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda announced that TAK-881-3001, a pivotal Phase 2/3 clinical trial in Primary Immunodeficiency Disease (PID) patients, met its primary endpoint.

7 weeks ago - Business Wire

Takeda Pharmaceutical Company Transcript: Study Update

Phase III studies show zasocitinib delivers rapid, durable skin clearance and significant quality-of-life improvements for moderate-to-severe plaque psoriasis, outperforming apremilast and placebo. The once-daily oral therapy demonstrated a strong safety profile and is positioned to expand the oral psoriasis market.

3 months ago - Transcripts

Takeda Pharmaceutical Company Slides: Study Update

Takeda Pharmaceutical Company has posted slides in relation to its latest quarterly earnings report, which was published on March 28, 2026.

3 months ago - Filings

Takeda's Zasocitinib Delivered Rapid and Durable Skin Clearance in a Convenient Once-Daily Pill, Affirming Promise to Reshape Psoriasis Care

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda's Zasocitinib Delivered Rapid and Durable Skin Clearance in a Convenient Once-Daily Pill, Affirming Promise to Reshape Psoriasis Care.

3 months ago - Business Wire

TrumpRx lists many medicines at prices higher than paid in UK

U.S. President Donald Trump pledged to make prescription drugs cheaper for Americans than anywhere in the world, but his TrumpRx.gov website is not delivering across the board lower prices than those ...

3 months ago - Reuters

Takeda Pharmaceutical Company Transcript: TD Cowen 46th Annual Health Care Conference

Three NMEs are set for launch following strong phase III results, with a new CEO transition and a focus on digital transformation. Oveporexton, zasocitinib, and rusfertide each target distinct markets with robust efficacy and safety profiles, while pipeline expansion and new indications are planned.

4 months ago - Transcripts

Takeda and Protagonist Announce U.S. Food and Drug Administration Accepts New Drug Application and Grants Priority Review for Rusfertide as a Potential First-in-Class Therapy for Polycythemia Vera

OSAKA, Japan & CAMBRIDGE, Mass. & NEWARK, Calif.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) and Protagonist Therapeutics, Inc. (“Protagonist”) (NASDAQ:PTGX) today announced that the U.S. Food and Dr...

4 months ago - Business Wire

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

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) today announced positive data from the pivotal Phase 3 KEPLER trial, which demonstrated that ENTYVIO® (vedolizumab) can off...

4 months ago - Business Wire

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

OSAKA, Japan & CAMBRIDGE, Mass.--(BUSINESS WIRE)--FDA Accepts New Drug Application and Grants Priority Review for Takeda's Oveporexton as a Potential First-in-Class Therapy for Narcolepsy Type 1.

4 months ago - Business Wire

Takeda deepens AI drug discovery push with $1.7 billion Iambic deal

Privately held Iambic said on Monday it has entered a multi-year partnership worth more than $1.7 billion with Japan's Takeda Pharmaceutical to use artificial intelligence to help design small-molecul...

4 months ago - Reuters

Iambic Announces Collaboration with Takeda to Advance AI-Driven Design of Small Molecules

SAN DIEGO & CAMBRIDGE, Mass.--(BUSINESS WIRE)--Iambic, a clinical-stage life science and technology company developing novel medicines using its AI-driven discovery and development platform, today ann...

4 months ago - Business Wire