Takeda Pharmaceutical Company Limited 보도자료

3월 14일 10:04

Takeda Announces Positive Topline Results from Phase 2 Study Evaluating Mezagitamab (TAK-079), a Potential Best-in-Class Anti-CD38 Monoclonal Antibody, for Primary Immune Thrombocytopenia

Takeda (TSE:4502/NYSE:TAK ) today announced positive topline results from a Phase 2, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability and efficacy of mezagitamab (TAK-079) in patients with persistent or chroni...

2월 29일 15:25

Takeda and Biological E. Limited Collaborate to Accelerate Access to Dengue Vaccine in Endemic Areas

Takeda (TSE:4502/NYSE:TAK ) and Biological E. Limited (BE), a leading India-based Vaccines and Pharmaceutical Company, today announced a strategic partnership to accelerate access to QDENGA®▽ (Dengue Tetravalent Vaccine [Live, Attenuated]) (TAK-00...

2월 29일 15:25

다케다, 바이올로지컬 E와 협력해 풍토병 지역 내 뎅기열 백신 이용 가속화

다케다(Takeda) (도쿄증권거래소: 4502/뉴욕증권거래소: TAK )와 인도의 선도적 백신 및 제약회사인 바이올로지컬 E(Biological E. Limited, BE)가 QDENGA®▽(뎅기 4가 백신[생백신, 약독백신])(TAK-003)의 다회용량바이알(MDV) 출시를 가속화하기 위한 전략적 파트너...

2월 11일 11:15

Takeda Intends to Rapidly Initiate the First Global Phase 3 Trials of TAK-861, an Oral Orexin Agonist, in Narcolepsy Type 1 in First Half of Fiscal Year 2024

Takeda (TSE:4502/NYSE:TAK ) today announced positive topline results from a randomized, double-blind, placebo-controlled, multiple dose Phase 2b trial evaluating TAK-861, an oral orexin receptor 2 (OX2R) agonist, in patients with narcolepsy type 1...

2월 2일 16:10

Takeda Announces Chief Financial Officer Succession

Takeda (TOKYO:4502/NYSE:TAK) today announced that Costa Saroukos, chief financial officer, has decided to leave Takeda to return to his home-country of Australia to be closer to family. Mr. Saroukos will step down as CFO, effective April 1, 2024 a...

2월 2일 16:10

다케다, 최고재무책임자 승계 발표

다케다(Takeda)(도쿄증권거래소: 4502/뉴욕증권거래소: TAK)는 최고재무책임자(CFO) 코스타 사루코스(Costa Saroukos)가 다케다를 떠나 가족들과 더 가까이 지내기 위해 고국인 호주로 돌아가기로 결정했다고 오늘 발표했다. 사루코스는 2024년 4월 1일부로 최고재무...

2월 2일 14:40

Takeda Announces Third-Quarter FY2023 Results; On-Track Towards Full-Year Management Guidance With Strong Momentum in Growth & Launch Products

Takeda (TOKYO:4502/NYSE:TAK) today announced financial results for the third quarter of fiscal year 2023 (period ended December 31, 2023). With year-to-date strong momentum in its Growth & Launch Products (+12.7% at CER) offsetting the significant...

2월 2일 14:40

다케다, 2023 회계연도 3분기 실적 발표하며 성장 및 출시 제품의 강력한 모멘텀으로 연간 경영 지침을 향해 순항

다케다(TOKYO:4502/NYSE:TAK)가 2023 회계연도 3분기(2023년 12월 31일 마감 기간)의 재무실적을 발표했다. 제네릭 약품 부문 진입 기업의 상당한 매출 영향을 상쇄하는 성장 및 출시 제품(Growth & Launch Products)(CER 기준 +12.7%)의 연간 강력한 모멘텀을 통해 ...

1월 31일 14:10

Takeda’s HYQVIA® Approved by European Commission as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Takeda (TSE:4502/NYSE:TAK ) today announced that the European Commission (EC) approved HYQVIA® [Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronidase] as maintenance therapy in patients of all ages with chronic inflammatory dem...

1월 31일 14:10

다케다의 하이큐비아®, 만성 염증성 탈수초성 다발성 신경병증(CIDP) 환자의 유지 요법으로 유럽연합 집행위원회가 승인

다케다(TSE:4502/NYSE:TAK )가 오늘 유럽연합 집행위원회(European Commission, EC)가 정맥 면역글로불린 요법(Intravenous Immunoglobulin Therapy, IVIG)으로 안정화 후 만성 염증성 탈수초성 다발성 신경병증(chronic inflammatory demyelinating polyneuropathy,...

1월 30일 14:06

Takeda’s GAMMAGARD LIQUID® Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Takeda (TSE:4502/NYSE:TAK ) today announced that the U.S. Food and Drug Administration (FDA) has approved GAMMAGARD LIQUID® [Immune Globulin Infusion (Human) 10% solution] as an intravenous immunoglobulin (IVIG) therapy to improve neuromuscular di...

1월 19일 11:00

Takeda Named Global Top Employer for Seventh Consecutive Year

Takeda (TSE:4502/NYSE:TAK ) today announced that for the seventh consecutive year, it has received global Top Employer® certification for 2024. Takeda is one of just 17 companies that received global recognition, and it was additionally certified ...

1월 19일 11:00

다케다, 7년 연속 전 세계 최우수 고용기업으로 선정

다케다(Takeda) (TSE:4502/NYSE:TAK) 가 오늘 7년 연속으로 2024년 전세계 최우수 고용기업® 인증을 받았다고 발표했다. 다케다는 전 세계적으로 인정을 받은 오직 17개 기업 중 하나이며, 24개국에서 최우수 고용기업으로 추가로 인증되었다. 우수고용협회(Top Empl...

1월 17일 14:33

U.S. FDA Approves Takeda’s HYQVIA® as Maintenance Therapy in Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Takeda (TSE:4502/NYSE:TAK ) today announced that the U.S. Food and Drug Administration (FDA) has approved HYQVIA® [Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronidase] for the treatment of chronic inflammatory demyelinating p...

2023년 12월 22일 13:59

Takeda Announces China NMPA Approval of LIVTENCITY® (maribavir) for the Treatment of Adults With Post-transplant Cytomegalovirus (CMV) Refractory to Prior Therapies

Takeda (TSE:4502/NYSE:TAK ) today announced that LIVTENCITY® (maribavir) has been approved by the National Medical Products Administration (NMPA) of China for the treatment of adult patients with post-hematopoietic stem cell transplant (HSCT) or s...

2023년 12월 17일 10:50

Takeda Receives Positive CHMP Opinion for HYQVIA® as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Takeda (TSE:4502/NYSE:TAK ) today announced the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of HYQVIA® [Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronid...

2023년 12월 17일 10:50

다케다, 만성 염증성 탈수초성 다발신경병증(CIDP) 환자의 하이큐비아 유지요법에 대해 긍정적 CHMP 의견 수신

다케다(도쿄증권거래소:4502/뉴욕증권거래소:TAK )는 오늘 유럽의약품청(EMA) 인체용약물사용자문위원회(CHMP)에서 만성 염증성 탈수초성 다발신경병증(CIDP) 환자에 대해 피하 면역글로불린 요법(IVIG)을 사용한 안정화 후 유지 요법으로의 하이큐비아(HYQVIA®)(재...

2023년 12월 6일 10:45

Takeda and The New York Academy of Sciences Announce 2024 Innovators in Science Award Winners

Takeda (TSE:4502/NYSE:TAK ) and The New York Academy of Sciences today announced the winners of the 2024 Innovators in Science Award for their excellence in, and commitment to, innovative science that has significantly advanced the field of resear...

2023년 11월 10일 17:40

Takeda Receives U.S. FDA Approval of FRUZAQLA™ for Previously Treated Metastatic Colorectal Cancer

Takeda (TSE:4502/NYSE:TAK ) today announced that the U.S. Food and Drug Administration (FDA) has approved FRUZAQLA™ (fruquintinib), an oral targeted therapy for adults with metastatic colorectal cancer (mCRC) who have been previously treated with ...

2023년 11월 10일 17:40

다케다, 치료 전력 있는 전이성 대장암 환자 치료제로 FRUZAQLA™에 대한 미국 식품의약국 승인 획득

다케다(Takeda)(도쿄증권거래소: 4502/뉴욕증권거래소: TAK )는 오늘 미국 식품의약국(FDA)이 FRUZAQLA™(프루킨티닙)를 승인했다고 발표했다. 프루자클라는 플루오로피리미딘(fluoropyrimidine-), 옥살리플라틴(oxaliplatin-), 이리노테칸(irinotecan-) 기반 화학요...

2023년 11월 10일 11:15

Takeda’s ADZYNMA Approved by U.S. FDA as the First and Only Recombinant ADAMTS13 Enzyme Replacement Therapy for the Treatment of Congenital Thrombotic Thrombocytopenic Purpura

Takeda (TSE:4502/NYSE:TAK ) today announced that the U.S. Food and Drug Administration (FDA) has approved ADZYNMA (ADAMTS13, recombinant-krhn) for the prophylactic and on-demand treatment of adult and pediatric patients with congenital thrombotic ...

2023년 11월 8일 10:48

Takeda Announces Late-Breaking Data from Phase 2b Study of TAK-279, an Investigational, Oral, Once-Daily TYK2 Inhibitor, in Patients with Active Psoriatic Arthritis at American College of Rheumatology Convergence Annual Meeting

Takeda (TSE:4502/NYSE:TAK) today announced that the company will present positive results from its randomized, double-blind, placebo-controlled, Phase 2b trial evaluating TAK-279, an investigational oral allosteric tyrosine kinase 2 (TYK2) inhibit...

2023년 10월 27일 11:40

Takeda Announces FY2023 H1 Results; Updates Full-Year Forecasts While Remaining on Track Towards Management Guidance

Takeda (TOKYO:4502/NYSE:TAK) today announced financial results for the first half of fiscal year 2023 (six months ended September 30, 2023), updating reported and Core forecasts and reconfirming Management Guidance for Core change at CER. Takeda c...