FDA Rejects Takeda's Eosinophilic Esophagitis Candidate, Asks For Additional StudyBenzinga • 12/22/21
Takeda Receives Positive CHMP Opinion for Vedolizumab IV for the Treatment of Active Chronic PouchitisBusiness Wire • 12/17/21
Takeda Drives Continued Scientific Leadership Through Real-World Evidence in Rare Hematological Diseases at ASH 2021Business Wire • 12/13/21
Takeda Announces Publication of Data from SOLSTICE, a Pivotal Phase 3 Trial for LIVTENCITY™ (Maribavir) in Post-Transplant Recipients With Cytomegalovirus (CMV) Infection (Refractory, With or Without Resistance)Business Wire • 12/08/21
Takeda Unveils New Research to Advance Patient Care in Hematology and Oncology at 63rd American Society of Hematology (ASH) Annual MeetingBusiness Wire • 12/07/21
Takeda's LIVTENCITY™ (maribavir) Now Available for Certain Individuals Ages 12 Years and Older With Post-Transplant Cytomegalovirus (CMV) Infection/Disease in the United StatesBusiness Wire • 12/02/21
Takeda Announces U.S. Corporate Social Responsibility (CSR) Program Aimed to Help Reduce Social DisparitiesBusiness Wire • 11/30/21
Takeda's LIVTENCITYTM (maribavir) Approved by U.S. FDA as the First and Only Treatment for People Ages 12 and Older with Post-Transplant Cytomegalovirus (CMV), Refractory (With or Without Genotypic Resistance) to Conventional Antiviral TherapiesBusiness Wire • 11/23/21
Takeda's Area Offices in Dubai, United Arab Emirates Certified Sustainable and InauguratedGlobeNewsWire • 11/16/21
Takeda Recommends Common-sense Policy Reforms Designed to Reduce Time to Diagnosis, Improve Access to Care for Patients with Rare DiseaseBusiness Wire • 11/04/21
5 Big Dividend Biotech and Pharmaceutical Stocks Have Strong Upside Potential24/7 Wall Street • 11/01/21
Takeda Pharmaceutical Company Limited (TAK) CEO Christophe Weber on Q2 2022 Results - Earnings Call TranscriptSeeking Alpha • 10/29/21
Takeda Pharmaceutical: Diversify Your Book With This Excellent Japanese Pharma PlaySeeking Alpha • 10/28/21