TAKTAKEDA PHARMACEUTICAL CO LTD

NYSE takeda.com


$ 12.94 $ 0.03 (0.23 %)    

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1,655,173
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$ 0.59
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News

OPINIONS

 takedas-livtencity-gains-approval-in-japan-for-post-transplant-cmv-treatment

Takeda ((TAK) today announced that LIVTENCITY® (maribavir) has been approved by the Japanese Ministry of Health, Labour and Wel...

 reported-earlier-takedas-mezagitamab-shows-results-for-rare-bleeding-disorder

Takeda ((TAK) today presented positive results from its Phase 2b, randomized, double-blind, placebo-controlled study evaluating...

Core News & Articles

− Approval Based on Results from Positive, Global, Phase 3 FRESCO-2 Trial− FRUZAQLA (fruquintinib) is the First Novel Targeted ...

 health-canada-expanded-marketing-authorization-for-takedas-hyqvia-as-replacement-therapy-for-primary-humoral-immunodeficiency-and-secondary-humoral-immunodeficiency-for-pediatric-patients

HyQvia®, which may be administered at home, will provide children and adolescents living with immunodeficiencies with a new tre...

 takeda-to-present-long-term-data-from-phase-3-advance-cidp-3-clinical-trial-of-hyqvia-in-patients-with-chronic-inflammatory-demyelinating-polyneuropathy-at-pns-annual-meeting

Favorable Findings from the Longest Public Clinical Study in CIDP Support HYQVIA as an Effective Long-Term Treatment Option for...

 whats-going-on-with-ovid-therapeutics-after-takedas-two-phase-3-epilepsy-studies-fail

Takeda Pharmaceutical reveals Phase 3 study data for Soticlestat (TAK-935) in treating Dravet and Lennox-Gastaut syndromes. In ...

 japan-pharma-giant-takedas-anti-seizure-treatment-flunks-in-two-late-stage-studies

Takeda Pharmaceutical released topline data from its Phase 3 studies, SKYLINE and SKYWAY, on Soticlestat for refractory Dravet ...

Core News & Articles

SKYLINE Study in Dravet Syndrome Narrowly Missed its Primary Endpoint of Reduction in Convulsive Seizure Frequency and Showed ...

 takeda-signs-option-agreement-with-ascentage-pharma-for-exclusive-license-of-olverembatinib-potential-third-generation-bcr-abl-tki-for-cml-and-other-hematological-cancers-license-excludes-mainland-china-hong-kong-macau-taiwan-and-russia

− Takeda to Receive Exclusive Option to License Global Rights to Olverembatinib in All Territories Outside of Mainland China, H...

 takeda-expands-partnership-with-partners-in-health-to-address-social-determinants-of-health-and-improve-access-to-care-in-massachusetts

The New Expanded Partnership Will Aim to Support the Dismantling of Systemic Barriers to Equity and Help Strengthen the Health ...

 blackstone-weighs-sale-of-japanese-pharma-firm-alinamin-report

Blackstone reportedly considers sale of Japanese consumer healthcare firm Alinamin Pharmaceutical (previously owned by Takeda) ...

 takeda-presents-phase-2b-results-for-narcolepsy-treatment-at-sleep-2024

Takeda ((TAK) will present today positive results from its Phase 2b trial of TAK-861 in narcolepsy type 1 (NT1) as late-breakin...

Core News & Articles

The four-year analysis showed superior progression-free survival (PFS) and improved tolerability for patients compared to a cur...

 takeda-gets-positive-chmp-opinion-for-recombinant-adamts13-in-congenital-thrombotic-thrombocytopenic-purpura

cTTP Is an Ultra-rare, Potentially Fatal Blood-Clotting Disorder with Limited Treatment Options; Untreated, Acute TTP Events Ha...

 takeda-canada-inc-concludes-letter-of-intent-loi-with-the-pan-canadian-pharmaceutical-alliance-pcpa-for-livtencity-maribavir-for-the-treatment-of-adults-with-a-post-transplant-cytomegalovirus-cmv-infection

Takeda Canada Inc. ("Takeda") is pleased to announce that it has completed negotiations with the pan-Canadian Pharmaceu...

 takedas-dengue-vaccine-gets-who-approval-eligible-for-un-procurement

Takeda's dengue vaccine, Qdenga, gains WHO prequalification, enabling UN agency procurement. Approved in multiple countries...

Core News & Articles

Scilex Holding Company (NASDAQ:SCLX, "Scilex" or "Company")))), an innovative revenue-generating company focuse...