Pharm
Maribavir
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Maribavir
, Livtencity
See Also
Letermovir
Ganciclovir
Cidofovir
Foscarnet
Valganciclovir
Cytomegalovirus
Indications
Resistant
Cytomegalovirus
Infection in Adults (and age >=12 years, weight >=35 kg)
Post-
Solid Organ Transplant
Post
Hematopoietic Stem Cell Transplant
cancer patients
Dosing
Adult (and age >=12 years, weight >=35 kg)
Take 400 mg orally twice daily
Mechanism
Benzimidazole riboside with activity against
Cytomegalovirus
Selective ATP competitive inhibitor for viral UL97 Kinase
Blocks viral DNA assembly and viral capsid transmission into cells
Pharmacokinetics
Good oral
Bioavailability
Half-Life
: 4.3 hours
Peak Activity after ingestion: 1 to 3 hours
Renal Excretion
Hepatic metabolism
Primarily
CYP3A4
substrate (with some metabolism by
CYP1A2
)
Adverse Effects
Common
Dysgeusia
Nausea
and
Vomiting
Diarrhea
Fatigue
Serious
Nephrotoxicity (8.5%)
Contrast with >21% for
Foscarnet
Neutropenia
(9.4%)
Contrast with >33% for
Ganciclovir
Safety
Unknown safety in pregnancy
Unknown safety in
Lactation
Drug Interactions
Strong
CYP3A4
Inducers (esp. Anticonvulsants) may decrease Maribavir levels
Carbamazepine
Increase Maribavir dose to 800 mg twice daily
Phenytoin
or
Phenobarbital
Increase Maribavir dose to 1200 mg twice daily
Maribavir is a weak
CYP3A4
and
P-gp
Inhibitor and may increase levels of drugs (monitor levels)
Tacrolimus
Cyclosporine
Resources
Maribavir (DailyMed)
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c94fc2c5-e840-4f18-b7d8-d5eacb26d3a0
References
(2022) Med Lett Drugs Ther 64: 193-4
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