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FDA Panel Votes on Maribavir for Post-Transplant CMV Infection

An FDA panel voted to recommend the use of maribavir for post-transplant CMV infection.

Maribavir global program leader at takedaDrug administrationAntimicrobial drugs advisory committeeNew drug applicationPriority reviewObi umehVice presidentMaribavir global program leader

FDA Advisory Committee Recommends Use of Investigational Drug Maribavir (TAK-620) to Treat Post-Transplant Recipients with Cytomegalovirus (CMV) Infection and Disease Refractory to Treatment With or Without Resistance

FDA Advisory Committee Recommends Use of Investigational Drug Maribavir (TAK-620) to Treat Post-Transplant Recipients with Cytomegalovirus (CMV) Infection and Disease Refractory to Treatment With or Without Resistance
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United statesEmily blumbergClin virolHuman cytomegalovirus nuclear egressInternational report on organ donationTakeda pharmaceutical company limitedThird international consensus guidelinesStage of nuclear egressTakeda pharmaceutical companyMediates disruption of nuclear laminaMaribavir global program leader at takedaDrug administrationWorld health organizationEuropean commissionAntimicrobial drugs advisory committeeExchange commission
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