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TAK

US8740602052

Produits pharmaceutiques

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18,18 ^USD	-0,19%		-2,41%	+17,13%

09/09	Takeda publie les données de phase 3 démontrant que l'oveporexton améliore les symptômes de la narcolepsie de type 1	CI
08/09	Le traitement de Pharvaris contre une maladie génétique atteint son objectif principal en phase finale d'essai	RE

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11:34	Takeda Pharmaceutical : Announces Planned Retirement of President of Research & Development Andy Plump
09/09	Takeda Publishes Phase 3 Data Demonstrating Oveporexton Improves Narcolepsy Type 1 Symptoms
09/09	New England Journal of Medicine Publishes Data from Phase 3 Studies Demonstrating Oveporexton (ORZEYFUL) Improved the Full Range of Narcolepsy Type 1 Symptoms and Quality of Life
08/09	Pharvaris' genetic disorder drug meets main goal in late-stage trial
04/09	After obesity, pharma seeks its next mega-blockbuster in sleep
04/09	Takeda Pharmaceutical Insider Sold Shares Worth $2,148,372, According to a Recent SEC Filing
01/09	Weave Bio and Takeda Enter Collaboration to Deploy Ai-Native Regulatory Automation Across Key Drug Development Activities
31/08	Takeda, Other Biotech Firms to Announce New Drug Pricing Deals With White House
31/08	Takeda, Other Biotech Firms to Announce New Drug Pricing Deals With White House
31/08	Protagonist Therapeutics' Own Pipeline Seen as Main Long-Term Growth Driver, Wedbush Says
31/08	Takeda Receives U.S. FDA Approval of MIMRYLO, Marking a Potential Shift in the Treatment Paradigm for Polycythemia Vera
31/08	Takeda Pharmaceutical Says US FDA Approves Rusfertide for Rare Type of Blood Cancer
31/08	Takeda Pharmaceutical Wins US Approval for New PV Treatment MIMRYLO
29/08	Takeda Pharmaceutical Company Limited Receives U.S. FDA Approval Of MIMRYLO For Treatment Of Erythrocytosis In Adults With Polycythemia Vera
29/08	Takeda Receives U.S. FDA Approval of MIMRYLO™ (rusfertide), Marking a Potential Shift in the Treatment Paradigm for Polycythemia Vera
28/08	US FDA approves Takeda, Protagonist's drug for rare blood cancer
28/08	Takeda's Mimrylo Gets FDA Approval to Treat Blood Cancer Condition
28/08	Novavax, Inc., Sanofi S.A., And Takeda Pharmaceutical Company Limited Receive Approvals For XFG-Adapted Nuvaxovid Formulation In The U.S., European Union And Japan For 2026-2027 Vaccination Season
28/08	Novavax's Nuvaxovid Approved in US, EU, Japan for 2026-2027 Season
24/08	Takeda Pharmaceutical : Provides Update on ADZYNMA (ADAMTS13, recombinant-krhn)
24/08	FDA places clinical hold on Regenxbio's gene therapy for Hunter Syndrome
24/08	Takeda's Orzeryful Approved in Japan as First Treatment Targeting Narcolepsy Type 1
24/08	Takeda Pharmaceutical Company Limited Receives Approval For Orzeyful (Oveporexton) To Treat Narcolepsy Type 1 In Japan
24/08	Takeda Secures Japan Approval for Orzeyful to Treat Narcolepsy Type 1
24/08	ORZEYFUL (oveporexton) Approved in Japan as the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1