Takeda’s Livtencity approved in Japan for CMV

24 June 2024

The Japanese Ministry of Health, Labor and Welfare (MHLW) has approved Livtencity (maribavir) for post-transplant cytomegalovirus (CMV) infection/disease that is refractory to existing anti-CMV therapies, Japanese pharma major Takeda (TYO: 4502) announced today.

The company noted that Livtencity is the first and only post-transplant anti-CMV treatment approved in Japan that targets and inhibits pUL97 kinase and its natural substrates.

European Commission (EC) granted approval for the marketing authorization application for Livtencity in this indication in November 2022, and China’s National Medical Products Administration (NMPA) did likewise in December last year. The drug is also approved in the USA and Canada. Takeda has previously projected $700 million to $800 million in peak sales for Livtencity.

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