Takeda Pharmaceutical Company Ltd
- Country
- 🇯🇵Japan
- Ownership
- -
- Established
- 1925-01-01
- Employees
- -
- Market Cap
- $47.5B
- Website
- http://www.takeda.co.jp/
FDA Approves Takeda's GAMMAGARD LIQUID ERC, First Ready-to-Use Low IgA Immunoglobulin Therapy for Primary Immunodeficiency
The U.S. FDA has approved GAMMAGARD LIQUID ERC as the only ready-to-use liquid immunoglobulin therapy with low IgA content for primary immunodeficiency treatment in patients aged two and older.
Day One Biopharmaceuticals Appoints Michael Vasconcelles as Head of R&D to Drive Pipeline Expansion
Day One Biopharmaceuticals has appointed Michael Vasconcelles, M.D., as Head of Research and Development, bringing over 25 years of oncology research and development expertise to the company.
Revolutionary Gene Therapy and BBB-Penetrating Treatments Transform Hunter Syndrome Treatment Landscape
RGX-121, a one-time gene therapy using AAV vector technology, is expected to receive regulatory approval in the second half of 2025, potentially offering lifelong benefits from a single infusion for Hunter Syndrome patients.
GC Biopharma's Hunterase Shows Significant Efficacy in Phase 3 Trial for Hunter Syndrome
GC Biopharma's Phase 3 clinical trial results for Hunterase (idursulfase beta) in Hunter Syndrome patients have been published in Genetics in Medicine, demonstrating significant improvements in functional mobility and metabolic markers.
Vima Therapeutics Emerges with $60M to Develop First Oral Therapy for Dystonia
Vima Therapeutics launched with $60 million Series A funding led by Atlas Venture to advance VIM0423, a potential first-in-class oral therapy for dystonia targeting muscarinic cholinergic receptors.
XOMA Royalty Acquires $30 Million Mezagitamab Rights from BioInvent as Anti-CD38 Antibody Advances to Phase 3
XOMA Royalty Corporation purchased BioInvent's future mezagitamab royalty and milestone rights for $20 million upfront plus $10 million upon FDA approval in IgA nephropathy.
Alzheimer's Drug Pipeline Shows Promising Diversity as 88 Trials Recruit Patients in 2025
The Alzheimer's drug development landscape has expanded significantly beyond anti-amyloid antibodies, with 88 different clinical trials currently recruiting patients and twelve Phase 3 trials expected to report results in 2025.
NextCell Pharma Strengthens Commercial Strategy with Appointment of MSC Therapy Expert Dr. Eric Strati
NextCell Pharma has appointed Dr. Eric Strati, former executive at Takeda, Mesoblast, and Novartis, to its Board of Advisors to advance commercial strategy for ProTrans, its type 1 diabetes cell therapy.
Takeda's Oveporexton Shows Promising Results in Phase 2b Trial for Narcolepsy Type 1
The New England Journal of Medicine published data showing Takeda's investigational oral orexin receptor 2 agonist oveporexton demonstrated significant improvements in wakefulness and reduced cataplexy events in narcolepsy type 1 patients.
Yaqrit Bolsters Leadership Team to Advance Late-Stage Liver Disease Treatments
Yaqrit has appointed Ronen Israel, a healthcare innovator and hedge fund strategist, to its management board, strengthening North American investment connectivity for its advanced liver disease portfolio.