Takeda Announces Approval of LIVTENCITY® (maribavir) in Japan for Post-Transplant Cytomegalovirus (CMV) Infection/Disease That Is Refractory to Existing Anti-CMV Therapies [Yahoo! Finance]
Takeda Pharmaceutical Company Limited American Depositary Shares (each representing 1/2 of a share of) (TAK)
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Source: Yahoo! Finance
CMV Is One of the Most Common and Serious Post-transplant Infections and Can Lead to Secondary Infections and Serious Consequences, Including Loss of Transplanted Organ and Failure of Graft OSAKA, Japan & CAMBRIDGE, Mass., June 24, 2024 BUSINESS WIRE )--Takeda ( TSE:4502/NYSE:TAK ) today announced that LIVTENCITY ® (maribavir) has been approved by the Japanese Ministry of Health, Labour and Welfare (MHLW) for post-transplant cytomegalovirus (CMV) infection/disease that is refractory to existing anti-CMV therapies. LIVTENCITY is the first and only post-transplant anti-CMV treatment approved in Japan that targets and inhibits pUL97 kinase and its natural substrates. "We are pleased by the approval of LIVTENCITY in Japan, which will provide the transplant community with a new option for treatment of post-transplant CMV infection in patients refractory to other therapies," said Yasushi Kajii, Head, R&D Japan Region at Takeda. "A diagnosis of CMV infection can be particularly challeng
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TAK
Sec Filings
- 9/26/24 - Form 6-K
- 8/22/24 - Form 144
- 7/31/24 - Form 6-K
- TAK's page on the SEC website