TAKTAKEDA PHARMACEUTICAL CO LTD

NYSE takeda.com


$ 14.88 $ -0.06 (-0.4 %)    

Thursday, 22-Aug-2024 15:59:58 EDT
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$ 14.88
$ 14.87 x 4,200
-- x --
-- - --
$ 12.58 - $ 16.39
2,329,312
na
25.14B
$ 0.60
$ 26.38
TBD
na
na ($ 0.00)
na
TBD na
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News

OPINIONS

 ascendis-hypoparathyroidism-drug-scores-fda-approval-as-first-and-only-treatment-replacing-takedas-drug-discontinued-due-to-supply-issues

FDA grants approval to Ascendis Pharma's Yorvipath (TransCon PTH) for adult hypoparathyroidism. Yorvipath offers continuous...

 why-is-japanese-drugmaker-takeda-pharmaceutical-stock-trading-higher-on-wednesday

Takeda Pharmaceutical stock rises following European Commission approval of Adzynma for treating ADAMTS13 deficiency in cTTP pa...

 takeda-2024-outlook-reaffirmed-expects-revenue-of--435t-and-core-eps-of-431-sees-adjusted-free-cash-flow-of-350b---450b

FY2024 Outlook (unchanged from May 2024) (Billion yen, except percentages and per share

 newly-listed-psoriasis-focused-alumis-attracts-analysts-attention-with-promising-lead-program-and-modest-valuation

Guggenheim Partners initiated coverage on Alumis, highlighting its lead asset ESK-001, a TYK2 inhibitor for plaque psoriasis an...

 eli-lillys-32b-morphic-deal-is-crucial-has-strategic-merit-despite-investor-attention-on-obesity-analyst

Eli Lilly's acquisition of Morphic highlights strategic expansion in Immunology, targeting α4β7 for ulcerative colitis and ...

 blackstone-nears-22b-deal-for-sale-of-japanese-supplement-maker-alinamin-report

Blackstone Inc. is reportedly finalizing a deal to sell Alinamin Pharmaceutical to MBK Partners for $2.17 billion. Blackstone a...

 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 ...

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