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Takeda s LIVTENCITYTM (maribavir) Approved by U S FDA as the First and Only Treatment for People Ages 12 and Older with Post-Transplant Cytomegalovirus (CMV), Refractory (With or Without Genotypic Resistance) to Conventional Antiviral Therapies

Takeda s LIVTENCITYTM (maribavir) Approved by U S FDA as the First and Only Treatment for People Ages 12 and Older with Post-Transplant Cytomegalovirus (CMV), Refractory (With or Without Genotypic Resistance) to Conventional Antiviral Therapies
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United statesShannon lowe emeryEl chaerChou marousekClin virolBenzimidazolel ribosideTakeda pharmaceuticals united states incTakeda pharmaceutical company limitedWire takeda pharmaceutical company limitedWorld health organizationThird international consensus guidelinesDrug administrationStage of nuclear egressTakeda pharmaceutical companyExchange commissionSpringer international publishing

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

Redirecting to Subgroup Analysis from Phase 3 Clinical Trial Supports Efficacy of Maribavir Over Conventional Therapies in Transplant Recipients With Cytomegalovirus Infection (Refractory, With or Without Resistance)

Redirecting to Subgroup Analysis from Phase 3 Clinical Trial Supports Efficacy of Maribavir Over Conventional Therapies in Transplant Recipients With Cytomegalovirus Infection (Refractory, With or Without Resistance)
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United statesDuarter maribavirClin virolHuman cytomegalovirus nuclear egressInternational report on organ donationTakeda pharmaceutical company limitedWorld health organizationThird international consensus guidelinesMeeting of the european society for bloodStage of nuclear egressExchange commissionSpringer international publishingMediates disruption of nuclear laminaMore than three timesBaseline receivingInvestigational drug maribavir achieved