TAK TAKEDA PHARMACEUTICAL CO LTD

NYSE takeda.com


$ 13.81 $ 0.08 (0.58 %)    

Tuesday, 14-Oct-2025 16:00:30 EDT
QQQ $ 598.50 $ -4.01 (-0.67 %)
DIA $ 463.08 $ 2.03 (0.44 %)
SPY $ 662.74 $ -0.81 (-0.12 %)
TLT $ 90.69 $ 0.29 (0.32 %)
GLD $ 382.95 $ 2.70 (0.71 %)
$ 13.8
$ 13.86
$ 13.79 x 30
$ 14.02 x 1
$ 13.74 - $ 13.89
$ 12.80 - $ 15.69
4,312,734
na
23.42B
$ 0.30
$ 32.53
TBD
na
na ($ 0.00)
na
TBD na
How to Read 10-K & 10-Q Reports To View SEC Filing Reports, Please Register or Sign In
# Filing Date Period End Date Type Report Link
No Data found
Guide for Analyst Ratings To View Analyst Ratings, Please Register or Sign In
# Date Analyst Firm Upside/Downside Price Target Change Rating Change Current Rating

News

OPINIONS

 takeda-taps-nabla-bios-generative-ai-platform-for-antibody-design-in-1-billion-pact

Nabla Bio partners with Takeda to use its AI platform JAM for designing antibodies, receiving upfront payments and potential su...

 johnson--johnson-in-talks-to-acquire-protagonist-therapeutics-report

Johnson & Johnson is in talks to buy Protagonist Therapeutics in a deal that could expand its immunology and cancer drug po...

 whats-going-on-with-nano-cap-galecto-stock-on-tuesday

Galecto stock spiked on heavy trading with no clear news, while the company highlights funding plans, pipeline updates, and cli...

 takeda-reports-results-from-firstlight-and-radiantlight-studies-showing-oveporexton-improves-wakefulness-cataplexy-severity-and-quality-of-life

– Takeda is the Leader in Orexin Science and is on Track to Submit Global Regulatory Applications Starting in Fiscal Year 2025–...

 on-friday-fda-approved-takedas-supplemental-application-for-vonvendi-expanding-the-indication-to-include-routine-prophylaxis-to-reduce-the-frequency-of-bleeding-episodes-in-adults-with-von-willebrand-disease

Takeda announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental Biologics License Application (...

 whats-going-on-with-takeda-stock-on-friday

Takeda stock steadies after early dip as FDA clears Ionis' Dawnzera for hereditary angioedema, posing fresh competition to ...

 ionis-pharma-wins-fda-nod-for-first-rna-targeted-therapy-for-rare-genetic-swelling-disorder

FDA approved Ionis' Dawnzera for hereditary angioedema, showing up to 87% attack reduction and strong results in switch pat...

 takeda-pharma-maintains-outlook-even-as-vyvanse-generics-hit-sales

Takeda reported a 30% rise in Q1 profit and beat EPS estimates, offsetting Vyvanse losses with growth in oncology, plasma, and ...

 takeda-reaffirms-fy2025-guidance-core-revenue-of-4530b-and-core-operating-profit-broadly-flat-at-1140b-core-eps-of-485

FY2025 Outlook (unchanged from May 2025)(Billion yen, except percentages and per share amounts)ItemFY2025 FORECASTFY2025 MANAGE...

 takeda-pharmaceutical-q1-adj-epads-052-beats-047-estimate-sales-766b-beat-753b-estimate

Takeda Pharmaceutical (NYSE:TAK) reported quarterly earnings of $0.52 per share which beat the analyst consensus estimate of $0...

 takeda-receives-fda-510k-clearance-for-hyhub-and-hyhub-duo-devices-for-patients-17-years-of-age-and-older-that-allow-hyqvia-to-be-transferred-from-vials-without-using-needle-in-home-environment-or-clinical-setting

HyHub and HyHub Duo Reduce the Number of Steps Required to Prepare HYQVIA1First Devices Customized for a Plasma-Derived Therapy...

 takedas-oveporexton-demonstrates-safety-and-efficacy-in-global-phase-3-studies-paving-way-for-new-narcolepsy-treatment

Both Phase 3 Studies Met all Primary and Secondary Endpoints Demonstrating Statistically Significant Improvements Across Sympto...

 takeda-gains-ec-approval-for-adcetris-in-combination-with-ecadd-chemotherapy-regimen-in-adult-patients-with-newly-diagnosed-stage-iib-with-risk-factorsiiiiv-hodgkin-lymphoma

- Approval Based on Positive Results from the Phase 3 HD21 Trial for Stage IIb with Risk Factors/III/IV Hodgkin Lymphoma- ADCET...

CLASS ACTION DEADLINES - JOIN NOW!

NEW CASE INVESTIGATION