<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title><![CDATA[Takeda Pharmaceutical Company Limited 보도자료 - 뉴스와이어]]></title><link>https://www.newswire.co.kr/?md=A10&amp;act=article&amp;no=21133></link><description><![CDATA[Takeda Pharmaceutical Company Limited 보도자료 - 뉴스와이어 RSS 서비스]]></description><lastBuildDate>Mon, 14 Sep 2026 03:48:20 +0900</lastBuildDate><copyright>Copyright (c) 2004~2026 Korea Newswire All rights reserved</copyright><image><url><![CDATA[https://file.newswire.co.kr/data/upfile/company_img/2013/12/12_1218276940_20131210091559_1132272665.jpg]]></url></image><language>ko-KR</language><item><title><![CDATA[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]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1042301</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK) announced that the New England Journal of Medicine  published results from two Phase 3 studies evaluating oveporexton (ORZEYFUL), an oral orexin receptor 2 (OX2R) agonist, in people with narcolepsy type 1 (NT1).[1] Oveporexton is the first and only medicine to treat the underlying cause of NT1.  “People living with nar...]]></description><pubDate>Thu, 10 Sep 2026 15:25:54 +0900</pubDate></item><item><title><![CDATA[Takeda Receives U.S. FDA Approval of MIMRYLO™ (rusfertide), Marking a Potential Shift in the Treatment Paradigm for Polycythemia Vera]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1041441</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) announced U.S. Food and Drug Administration (FDA) approval  of the New Drug Application (NDA)* for MIMRYLO™ (rusfertide) for the treatment of erythrocytosis in adults with polycythemia vera (PV), a blood cancer.  MIMRYLO is a first-in-class hepcidin mimetic designed to regulate iron distribution in the body and red bl...]]></description><image><url><![CDATA[https://file.newswire.co.kr/data/datafile2/thumb/2026/08/1028147215_20260830141028_4190573751.jpg]]></url></image><pubDate>Sun, 30 Aug 2026 14:12:46 +0900</pubDate></item><item><title><![CDATA[ORZEYFUL (oveporexton) Approved in Japan as the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1041019</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TOKYO:4502/NYSE:TAK ) announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) approved the use of ORZEYFUL (oveporexton) for the treatment of narcolepsy type 1 (NT1, narcolepsy with cataplexy) in adults. ORZEYFUL is a first-in-class oral orexin receptor 2 (OX2R) agonist and the only medicine indicated in Japan to treat ...]]></description><image><url><![CDATA[https://file.newswire.co.kr/data/datafile2/thumb/2026/08/31017998_20260824151642_7630859430.jpg]]></url></image><pubDate>Mon, 24 Aug 2026 16:00:55 +0900</pubDate></item><item><title><![CDATA[U.S. FDA Approves Takeda’s ORZEYFUL™ (oveporexton), the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1040045</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) announced that the U.S. Food and Drug Administration (FDA) approved  ORZEYFUL™ (oveporexton), an oral orexin receptor 2 (OX2R) agonist, for the treatment of narcolepsy type 1 (NT1, narcolepsy with cataplexy) in adults.* The persistent 24-hour nature of NT1 is driven by orexin deficiency and can severely impact people’...]]></description><pubDate>Thu, 06 Aug 2026 10:43:09 +0900</pubDate></item><item><title><![CDATA[Takeda Announces FY2026 First Quarter Results, Near-Term Launch Preparations and Pipeline Progress on Track]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1039673</link><description><![CDATA[OSAKA, Japan--(Business Wire/Korea Newswire)--Takeda (TOKYO:4502/NYSE:TAK ) announced financial results for the first quarter of fiscal year 2026 (April 1, 2026 to June 30, 2026), marking a period of disciplined execution and operational momentum. Takeda leveraged the resilient performance of its core in-line portfolio to support its long-term strategy, advancing commercial launch preparati...]]></description><pubDate>Thu, 30 Jul 2026 15:52:06 +0900</pubDate></item><item><title><![CDATA[Takeda’s Zasocitinib Demonstrates Consistent, High Rates of Skin Clearance Across the Body, Including Hard-to-Treat and High-Impact Sites, in Phase 3 Psoriasis Studies]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1038838</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) announced new data from the two pivotal Phase 3 studies of zasocitinib (TAK-279), a next-generation, highly selective and potent oral tyrosine kinase 2 (TYK2) inhibitor, in adults with moderate-to-severe plaque psoriasis (PsO).[1] Presented at the 2026 American Academy of Dermatology (AAD) Innovation Academy, these se...]]></description><pubDate>Sun, 19 Jul 2026 13:05:00 +0900</pubDate></item><item><title><![CDATA[Takeda and the Indonesian Government Announce Landmark Collaboration to Strengthen Healthcare Resilience and Expand Access to Lifesaving Plasma-Derived Medicinal Products]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1038436</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass. & JAKARTA, Indones--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK) and the Indonesian Government (the Ministry of Health, the Ministry of Investment and Downstream Industry/BKPM and the Coordinating Ministry for Economic Affairs) today announced a groundbreaking collaboration aimed at strengthening Indonesia’s plasma ecosystem and supporting more equitable access to lifesaving plasma-...]]></description><pubDate>Mon, 13 Jul 2026 09:28:27 +0900</pubDate></item><item><title><![CDATA[Takeda Announces New Assignments of Directors and Appointment of Julie Kim as Representative Director, President and CEO]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1037286</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--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 Representative Director, President and Chief Executive Officer.  During the 150th Annual General Meeting of Shareholders, which took place in Osaka, Japan, shareholders elected Julie as a new internal d...]]></description><pubDate>Wed, 24 Jun 2026 16:32:19 +0900</pubDate></item><item><title><![CDATA[New Pivotal Study Data Show Takeda’s Oveporexton Improved Daily Function, Cognition and Nighttime Sleep for People with Narcolepsy Type 1]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1036688</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today presented additional results from two pivotal studies at SLEEP 2026, showing oveporexton (TAK-861), an oral orexin receptor 2 (OX2R)-selective agonist, improved daily functioning as well as cognitive and sleep-related symptoms associated with narcolepsy type 1 (NT1).[1,2,3] Oveporexton is designed to address the...]]></description><pubDate>Tue, 16 Jun 2026 16:55:53 +0900</pubDate></item><item><title><![CDATA[Takeda’s Zasocitinib Significantly Outperforms Deucravacitinib in Head-to-Head Phase 3 Psoriasis Study, Promising to Redefine Oral Treatment Expectations]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1036418</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) announced positive topline results for the Phase 3, randomized, multicenter, double-blind study comparing zasocitinib (TAK-279), an investigational, next-generation, highly selective and potent oral tyrosine kinase 2 (TYK2) inhibitor, to deucravacitinib in adults with moderate-to-severe plaque psoriasis (PsO).  In the...]]></description><pubDate>Fri, 12 Jun 2026 10:51:54 +0900</pubDate></item><item><title><![CDATA[Takeda Announces FY2025 Full Year Results and FY2026 Outlook, Highlighted by Excellent Pipeline Progress and Solid FY2025 Results]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1034387</link><description><![CDATA[OSAKA, Japan--(Business Wire/Korea Newswire)--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 its latest FY2025 Management Guidance, reflecting strong OPEX savings, mitigating revenue headwinds while continuing to invest in future growth.  Key Highlights for FY2025  ·	Rev...]]></description><pubDate>Wed, 13 May 2026 16:11:12 +0900</pubDate></item><item><title><![CDATA[Takeda Announces Positive Topline Results from Pivotal Phase 2/3 Clinical Trial of TAK-881 in Primary Immunodeficiency Disease (PID)]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1033838</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today announced that TAK-881-3001, a pivotal Phase 2/3 clinical trial in patients with Primary Immunodeficiency Disease (PID), met its primary endpoint, which demonstrated pharmacokinetic (PK) comparability between the investigational TAK-881 [Immune Globulin Subcutaneous (Human), 20% Solution (SCIG 20%) with Recombin...]]></description><pubDate>Wed, 06 May 2026 16:25:00 +0900</pubDate></item><item><title><![CDATA[다케다, 원발성 면역결핍질환 대상 TAK-881의 중추적 제2/3상 임상시험에서 긍정적인 주요 결과 발표]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1033839</link><description><![CDATA[오사카, 일본 & 케임브리지, 메사추세츠--(Business Wire/뉴스와이어)--다케다(Takeda)(TSE:4502/NYSE:TAK )가 원발성 면역결핍질환(PID) 환자를 대상으로 한 중추적 제2/3상 임상시험인 TAK-881-3001이 임상시험용 TAK-881(재조합 인간 히알루로니다제를 병용한 면역글로불린 피하(인간), 20% 용액(SCIG 20%))과 하이큐비아(재조합 인간 히알루로니다제를 병용한 면역글로불린 주입액(인간) 10%) 간의 약동학적(PK) 동등성이 입증한 1차 평가변...]]></description><pubDate>Wed, 06 May 2026 16:25:00 +0900</pubDate></item><item><title><![CDATA[Takeda’s Zasocitinib Delivered Rapid and Durable Skin Clearance in a Convenient Once-Daily Pill, Affirming Promise to Reshape Psoriasis Care]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1031272</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK) today announced new data from the two pivotal Phase 3 studies of zasocitinib (TAK-279), a next-generation, highly selective oral tyrosine kinase 2 (TYK2) inhibitor, in adults with moderate-to-severe plaque psoriasis (PsO).[1] Presented as a late-breaking abstract at the 2026 American Academy of Dermatology (AAD) Annual...]]></description><pubDate>Sun, 29 Mar 2026 11:45:00 +0900</pubDate></item><item><title><![CDATA[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]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1029612</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass. & NEWARK, Calif.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) and Protagonist Therapeutics, Inc. (“Protagonist”) (NASDAQ:PTGX ) today announced that the U.S. Food and Drug Administration (FDA) accepted the New Drug Application (NDA) and granted Priority Review for rusfertide. Rusfertide is an investigational, first-in-class hepcidin mimetic peptide therapeutic for the treatment ...]]></description><pubDate>Wed, 04 Mar 2026 11:11:15 +0900</pubDate></item><item><title><![CDATA[Positive Phase 3 Data Demonstrate Potential for ENTYVIO® (vedolizumab) to Address Treatment Gap for Children and Adolescents with Moderate to Severe Ulcerative Colitis]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1028961</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today announced positive data from the pivotal Phase 3 KEPLER trial, which demonstrated that ENTYVIO® (vedolizumab) can offer the possibility of clinical remission for patients ages 2 and older with moderately to severely active ulcerative colitis (UC), a chronic inflammatory disease of the gastrointestinal tract and ...]]></description><pubDate>Fri, 20 Feb 2026 09:57:01 +0900</pubDate></item><item><title><![CDATA[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]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1028534</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today announced that the U.S. Food and Drug Administration (FDA) accepted its New Drug Application (NDA) and granted Priority Review for oveporexton (TAK-861) for the treatment of narcolepsy type 1 (NT1). Oveporexton is an investigational oral orexin receptor 2 (OX2R)-selective agonist designed to address the underlyi...]]></description><pubDate>Tue, 10 Feb 2026 17:30:10 +0900</pubDate></item><item><title><![CDATA[Takeda Reports Third-Quarter FY2025 Results: Updates Full Year Outlook to Reflect VYVANSE® Generics Impact, OPEX Discipline and FX Tailwind; Progressing Toward Three Transformative Launches Ahead]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1027836</link><description><![CDATA[OSAKA, Japan--(Business Wire/Korea Newswire)--Takeda (TOKYO:4502/NYSE:TAK ) today announced earnings results for the third quarter of fiscal year 2025 (nine months ended December 31, 2025). The gap between incremental Growth &amp; Launch Products revenue and VYVANSE erosion is narrowing, and operational efficiencies drove year-on-year reductions in operating expenses, including R&amp;D. The...]]></description><pubDate>Thu, 29 Jan 2026 15:52:14 +0900</pubDate></item><item><title><![CDATA[Takeda and Protagonist Announce Submission of New Drug Application (NDA) for Rusfertide for Treatment of Polycythemia Vera (PV)]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1026463</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass. & NEWARK, Calif.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) and Protagonist Therapeutics (Nasdaq: PTGX) (“Protagonist”) announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) seeking approval of rusfertide for the treatment of adults with polycythemia vera (PV). Rusfertide is an investigational first-in-class subcutaneously admi...]]></description><pubDate>Tue, 06 Jan 2026 09:04:17 +0900</pubDate></item><item><title><![CDATA[Takeda’s Zasocitinib Landmark Phase 3 Plaque Psoriasis Data Show Promise to Deliver Clear Skin in a Once-Daily Pill, Catalyzing a New Era of Treatment]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1025678</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today announced positive topline results for the two pivotal Phase 3 randomized, multicenter, double-blind, placebo- and active comparator-controlled studies of zasocitinib (TAK-279), a next-generation, highly selective oral tyrosine kinase 2 (TYK2) inhibitor, in adults with moderate-to-severe plaque psoriasis (PsO). ...]]></description><pubDate>Thu, 18 Dec 2025 17:09:37 +0900</pubDate></item><item><title><![CDATA[Protagonist and Takeda Present Longer-Term Data at ASH 2025 Showing Rusfertide Delivers Durable Response and Hematocrit Control in Polycythemia Vera]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1024802</link><description><![CDATA[NEWARK, Calif. & OSAKA, Japan & CAMBRIDGE, Mass--(Business Wire/뉴스와이어)--Protagonist Therapeutics, Inc. (“Protagonist”) (NASDAQ:PTGX ) and Takeda (TSE:4502/NYSE:TAK ) announce that new 52-week results from the pivotal Phase 3 VERIFY study evaluating rusfertide in patients with polycythemia vera (PV) will be presented in an oral presentation at the 67th American Society of Hematology (ASH) Annual Meeting and Expositio...]]></description><pubDate>Sun, 07 Dec 2025 16:00:15 +0900</pubDate></item><item><title><![CDATA[Takeda Presents New Data Showing Mezagitamab (TAK-079) Sustained Effect on Kidney Function 18 Months After Treatment in Primary IgA Nephropathy]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1022555</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today announced new interim data from the Phase 1b, open-label, proof-of-concept study of subcutaneous mezagitamab (TAK-079), an anti-CD38 monoclonal antibody with disease-modifying potential, in primary immunoglobulin A (IgA) nephropathy. Data from the study showed that kidney function (eGFR) remained stable in patie...]]></description><pubDate>Sun, 09 Nov 2025 09:50:08 +0900</pubDate></item><item><title><![CDATA[New Phase 3 Data Show Takeda’s Dengue Vaccine Delivers 7 Years of Sustained Protection Against Infection and Hospitalization]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1022085</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) announced the completion of the 7-year pivotal Phase 3 Tetravalent Immunization against Dengue Efficacy Study  (TIDES) trial evaluating its dengue vaccine, QDENGA®▼(Dengue Tetravalent Vaccine [Live, Attenuated]) (TAK-003). These data, including an exploratory analysis of a booster dose, confirm the favorable benefit a...]]></description><pubDate>Tue, 04 Nov 2025 08:39:39 +0900</pubDate></item><item><title><![CDATA[Takeda Reports First Half FY2025 Results, with Business Fundamentals Tracking as Planned. Updates Full Year Outlook to Reflect FX Impact and Pipeline Impairment. On Track for Multiple Regulatory Filings This Fiscal Year]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1021836</link><description><![CDATA[OSAKA, Japan--(Business Wire/Korea Newswire)--Takeda (TOKYO:4502/NYSE:TAK ) today announced earnings results for the first half of fiscal year 2025 (six months ended Sep 30, 2025) and updated its full-year outlook.  Takeda chief executive officer, Christophe Weber, commented: “Takeda’s fiscal year 2025 first half results are consistent with our expectations for core business progress in thi...]]></description><pubDate>Thu, 30 Oct 2025 16:51:19 +0900</pubDate></item><item><title><![CDATA[Takeda Enters Global Strategic Partnership with Innovent Biologics to Bolster Oncology Pipeline with Next-Generation Investigational Medicines for Treatment of Solid Tumors]]></title><link>https://www.newswire.co.kr/newsRead.php?no=1021129</link><description><![CDATA[OSAKA, Japan & CAMBRIDGE, Mass.--(Business Wire/Korea Newswire)--Takeda (TSE:4502/NYSE:TAK ) today announced that it has entered into a license and collaboration agreement with Innovent Biologics (HKEX: 01801) for the development, manufacturing and commercialization of two late-stage oncology medicines, IBI363 and IBI343, worldwide outside of Greater China.* IBI363 is being evaluated in non-small cell lung an...]]></description><pubDate>Wed, 22 Oct 2025 14:50:39 +0900</pubDate></item></channel></rss>