Wednesday, October 2, 2024

CATEGORY

Takeda

Attention Deficit Hyperactivity Disorder Treatment Access Boosted as President Endorses Adderall XR Reimbursement

Key TakeawaysThe President's recommendation supports the reimbursement of Adderall XR for attention deficit hyperactivity disorder treatment. The decision aims to improve access to...

Takeda Receives Approval for FRUZAQLA in Japan to Treat Advanced Colorectal Cancer

Key TakeawaysTakeda's FRUZAQLA (fruquintinib), an innovative targeted therapy, has been approved in Japan for unresectable advanced colorectal cancer. The approval is based on...

Lupin Secures Patent Licensing to Commercialize Vonoprazan for Acid Peptic Disorders in India

Key Takeaways:Lupin Limited has signed a non-exclusive patent license agreement with Takeda Pharmaceutical Company to commercialize Vonoprazan Tablets in the Indian market under...

Pharmaceutical Giants Alkem and Takeda Join Forces to Bring Vonoprazan to India

Key TakeawaysAlkem Laboratories has entered a landmark licensing agreement with Takeda Pharmaceutical Company to commercialize Vonoprazan, a novel medication for gastrointestinal disorders, in...

European Commission Approves ADZYNMA® as the First Recombinant Therapy for cTTP

Takeda has received European Commission approval for ADZYNMA® (recombinant ADAMTS13), making it the first and only recombinant enzyme replacement therapy available for congenital thrombotic...

Results Highlight Takeda’s Strong Q1 Performance: Growth & Launch Products Lead Revenue Surge

Results from Takeda (TOKYO:4502/NYSE) were announced today, detailing earnings for the first quarter of fiscal year 2024 (period ended June 30, 2024). The company...

Takeda’s New Data on Mezagitamab Shows Promise in ITP Treatment

Takeda Pharmaceuticals has announced encouraging results from its Phase 2b study of mezagitamab, showing potential to transform the treatment of primary immune thrombocytopenia (ITP)....

Cytomegalovirus Treatment: Takeda’s LIVTENCITY® Approved in Japan for Post-Transplant Infections

Takeda has announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) approved LIVTENCITY® (maribavir) for treating post-transplant cytomegalovirus (CMV) infection/disease refractory to...

Demyelinating Polyneuropathy Treatment: Takeda’s HYQVIA® Shows Long-Term Safety and Efficacy

Takeda has presented favorable data from the Phase 3 ADVANCE-CIDP 3 clinical trial, a long-term study evaluating HYQVIA® for chronic inflammatory demyelinating polyneuropathy...

Leukemia Treatment Advancements: Takeda and Ascentage Pharma Partner on Olverembatinib Development

In a significant move within the pharmaceutical industry, Takeda and Ascentage Pharma have signed an option agreement for the development and commercialization of olverembatinib,...

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