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Home » A new first as FDA approves Takeda drug to treat CMV in transplant recipients
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A new first as FDA approves Takeda drug to treat CMV in transplant recipients

Nov. 24, 2021
By Michael Fitzhugh
Following an FDA priority review, Takeda Pharmaceutical Co. Ltd.'s oral antiviral, maribavir, has won U.S. approval as the first drug in the country to treat resistant cytomegalovirus (CMV) infection and disease in adult and pediatric transplant recipients. The drug will be marketed as Livtencity.
BioWorld Regulatory Infection Japan U.S. FDA

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