LIVTENCITY (Maribavir Tablets) – Post Transplant CMV Infection | HongKong DengYue Medicine
- Generic Name/Brand Name: Maribavir Tablets/LIVTENCITY
- Indications: Post-transplant CMV infection/disease
- Dosage Form: Tablets
- Specification: 0.2g x 56 tablets
LIVTENCITY Application Scope
Indicated for treatment of adults and pediatric patients (12 years of age and older and weighing at least 35 kg) with post-transplant cytomegalovirus (CMV) infection/disease that is refractory (with or without genotypic resistance) to ganciclovir, valganciclovir, cidofovir or foscarnet.

LIVTENCITY Characteristics
Ingredients:
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Active Ingredient: Maribavir
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Inactive Ingredients: FD&C Blue #1, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, sodium starch glycolate, titanium dioxide, and talc.
Properties:
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Pharmacological Class: Cytomegalovirus (CMV) pUL97 kinase inhibitor.
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Mechanism of Action: Inhibits the CMV pUL97 kinase, which is essential for viral DNA replication.
Packaging Specification:
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Form: Oral tablets
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Strength: 200 mg per tablet
Storage:
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Conditions: Store at 20°C to 25°C (68°F to 77°F).
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Stability: Shelf life is 30 months from the date of manufacture when stored under recommended conditions.
Expiry Date:
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Refer to the expiration date printed on the packaging.
Executive Standard:
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Manufactured in compliance with applicable pharmaceutical manufacturing standards.
Approval Number:
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Approved by the U.S. FDA on November 23, 2021.
Date of Revision:
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Refer to the latest prescribing information for the most recent revision date.
Manufacturer:
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Takeda Pharmaceuticals USA
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Guidelines for the Use of LIVTENCITY
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Dosage and Administration:
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Recommended Dose: 400 mg (two 200 mg tablets) taken orally twice daily with or without food.
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Administration: Oral tablets
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Missed Dose: If a dose is missed, take it as soon as remembered unless it is less than 12 hours until the next dose. Do not double doses to make up for a missed dose.
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Adverse Reactions:
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Common Adverse Reactions: Headache
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Serious Adverse Reactions:
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Potential for reduced therapeutic effect when coadministered with certain drugs
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Risk of virologic failure during treatment and relapse post-treatment
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Risk of reduced antiviral activity when coadministered with ganciclovir and valganciclovir
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Contraindications: None identified.
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Precautions: Monitor CMV DNA levels and check for resistance if patient does not respond to treatment.
LIVTENCITY Interactions
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Coadministration with ganciclovir or valganciclovir is not recommended due to antagonistic effects.
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Strong CYP3A4 inducers may reduce maribavir exposure; dose adjustments needed when coadministered with certain anticonvulsants (e.g. carbamazepine, phenytoin, phenobarbital).
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Has potential to increase concentrations of immunosuppressant drugs that are CYP3A4 / P-gp substrates (tacrolimus, cyclosporine, sirolimus, everolimus); monitoring required.
Note:
- If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
- This content is for reference only. Prescription drugs must be used under a doctor’s guidance and purchased from authorized sources.










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