LIVTENCITY is indicated for the 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 to treatment (with or without genotypic resistance) with ganciclovir, valganciclovir, cidofovir or foscarnet [see Use in Specific Populations (8.4) and Clinical Studies (14)].

{ "type": "p", "children": [], "text": "LIVTENCITY is indicated for the 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 to treatment (with or without genotypic resistance) with ganciclovir, valganciclovir, cidofovir or foscarnet [see Use in Specific Populations (8.4) and Clinical Studies (14)]." }

The recommended dosage in adults and pediatric patients (12 years of age and older and weighing at least 35 kg) is 400 mg (two 200 mg tablets) taken orally twice daily with or without food [see Use in Specific Populations (8.4), Clinical Pharmacology (12.3) and Clinical Studies (14)].

If LIVTENCITY is coadministered with carbamazepine, increase the dosage of LIVTENCITY to 800 mg (four 200 mg tablets) twice daily [see Drug Interactions (7.3)].

If LIVTENCITY is coadministered with phenytoin or phenobarbital, increase the dosage of LIVTENCITY to 1,200 mg (six 200 mg tablets) twice daily [see Drug Interactions (7.3)].

The immediate-release tablets can be taken as whole, dispersed or crushed tablets by mouth, or as dispersed tablets through a nasogastric or orogastric tube (French size 10 or larger). The suspension may be prepared ahead of time and stored at room temperature for up to 8 hours.

Administration of Dispersed Tablets or Crushed Tablets by Mouth

Administration of Dispersed Tablets through a Nasogastric (NG) or Orogastric (OG) Tube

Tablet: 200 mg, blue, oval shaped convex tablet debossed with "SHP" on one side and "620" on the other side.

{ "type": "p", "children": [], "text": "Tablet: 200 mg, blue, oval shaped convex tablet debossed with \"SHP\" on one side and \"620\" on the other side." }

None.

{ "type": "p", "children": [], "text": "None." }

LIVTENCITY may antagonize the antiviral activity of ganciclovir and valganciclovir by inhibiting human CMV pUL97 kinase, which is required for activation/phosphorylation of ganciclovir and valganciclovir. Coadministration of LIVTENCITY with ganciclovir or valganciclovir is not recommended [see Drug Interactions (7.1) and Microbiology (12.4)].

Virologic failure due to resistance can occur during and after treatment with LIVTENCITY. Virologic relapse during the post-treatment period usually occurred within 4-8 weeks after treatment discontinuation. Some maribavir pUL97 resistance-associated substitutions confer cross-resistance to ganciclovir and valganciclovir. Monitor CMV DNA levels and check for maribavir resistance if the patient is not responding to treatment or relapses [see Microbiology (12.4) and Clinical Studies (14.1)].

The concomitant use of LIVTENCITY and certain drugs may result in potentially significant drug interactions, some of which may lead to reduced therapeutic effect of LIVTENCITY or adverse reactions of concomitant drugs [see Drug Interactions (7)].

See Table 4 for steps to prevent or manage these possible or known significant drug interactions, including dosing recommendations. Consider the potential for drug interactions prior to and during LIVTENCITY therapy; review concomitant medications during LIVTENCITY therapy and monitor for adverse reactions.

Maribavir is primarily metabolized by CYP3A4. Drugs that are strong inducers of CYP3A4 are expected to decrease maribavir plasma concentrations and may result in reduced virologic response; therefore, coadministration of LIVTENCITY with these drugs is not recommended, except for selected anticonvulsants [see Dosage and Administration (2.2) and Drug Interactions (7.3)].

Use with Immunosuppressant Drugs

LIVTENCITY has the potential to increase the drug concentrations of immunosuppressant drugs that are CYP3A4 and/or P-glycoprotein (P-gp) substrates where minimal concentration changes may lead to serious adverse events (including tacrolimus, cyclosporine, sirolimus and everolimus). Frequently monitor immunosuppressant drug levels throughout treatment with LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust the immunosuppressant dose, as needed [see Drug Interactions (7.3) and Clinical Pharmacology (12.3)].

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The safety of LIVTENCITY was evaluated in one Phase 3 multicenter, randomized, open-label, active-control trial in which 352 adult transplant recipients were randomized, and treated with LIVTENCITY (N=234) or Investigator-Assigned Treatment (IAT) consisting of monotherapy or dual therapy with ganciclovir, valganciclovir, foscarnet, or cidofovir as dosed by the investigator (N=116) for up to 8-weeks following a diagnosis of CMV infection/disease refractory to treatment (with or without genotypic resistance) with ganciclovir, valganciclovir, foscarnet or cidofovir. The mean treatment durations (SD) for LIVTENCITY and IAT were 48.6 (± 13.82) and 31.2 (± 16.91) days, respectively. The most common adverse events occurring in more than 10% of subjects receiving LIVTENCITY are outlined in Table 2.

<div class="scrollingtable"><table width="75%"> <caption> <span>Table 2: Adverse Events (All Grades) Reported in &gt;10% of Subjects in the LIVTENCITY Group in Trial 303</span> </caption> <col align="left" valign="top" width="32%"/> <col align="center" valign="top" width="36%"/> <col align="center" valign="top" width="32%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule" valign="middle">ADVERSE EVENT</th><th align="center" class="Rrule">LIVTENCITY<br/> N=234<br/> (%)</th><th align="center" class="Rrule">IAT<a class="Sup" href="#footnote-1" name="footnote-reference-1">*</a> <br/> N=116<br/> (%)</th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-1" name="footnote-1">*</a> </dt> <dd>IAT (Investigator-Assigned Treatment) included monotherapy or dual therapy with ganciclovir, valganciclovir, foscarnet, or cidofovir as dosed by the investigator.</dd> <dt> <a href="#footnote-reference-2" name="footnote-2">†</a> </dt> <dd>taste disturbance includes the following reported preferred terms: ageusia, dysgeusia, hypogeusia and taste disorder.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Taste disturbance<a class="Sup" href="#footnote-2" name="footnote-reference-2">†</a></td><td align="center" class="Rrule">46</td><td align="center" class="Rrule">4</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Nausea</td><td align="center" class="Rrule">21</td><td align="center" class="Rrule">22</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Diarrhea</td><td align="center" class="Rrule">19</td><td align="center" class="Rrule">21</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Vomiting</td><td align="center" class="Rrule">14</td><td align="center" class="Rrule">16</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">Fatigue</td><td align="center" class="Rrule">12</td><td align="center" class="Rrule">9</td> </tr> </tbody> </table></div>

Similar proportions of subjects experienced serious adverse events (38% in the LIVTENCITY group and 37% in the IAT group). The most common serious adverse event in both treatment groups occurred in the Infections and Infestations System Organ Class (SOC) (23% in the LIVTENCITY group and 15% in the IAT group) with CMV infection and disease being the most common in both groups.

A higher proportion of subjects in the IAT group discontinued study medication due to an adverse event compared to the LIVTENCITY group (32% in the IAT group vs 13% in the LIVTENCITY group). The most commonly reported causes that led to study drug discontinuation were neutropenia (9%) and acute kidney injury (5%) in the IAT group and dysgeusia, diarrhea, nausea, and recurrence of underlying disease (each reported at 1%) in the LIVTENCITY group.

Taste disturbance occurred in 46% of subjects treated with LIVTENCITY. These events rarely led to discontinuation of LIVTENCITY (1%) and, for 37% of the subjects, these events resolved while on therapy (median duration 43 days; range 7 to 59 days). For the subjects with ongoing taste disturbance after drug discontinuation, resolution occurred in 89%. In subjects with resolution of symptoms after drug discontinuation, the median duration of symptoms off treatment was 6 days (range 2 to 85 days).

Laboratory Abnormalities

Selected laboratory abnormalities reported in subjects with refractory (with or without genotypic resistance) CMV infections in Trial 303 are presented in Table 3.

<div class="scrollingtable"><table width="75%"> <caption> <span>Table 3: Selected Laboratory Abnormalities Reported in Trial 303</span> </caption> <col align="left" valign="top" width="34%"/> <col align="center" valign="top" width="33%"/> <col align="center" valign="top" width="33%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule" valign="middle">Laboratory Parameter</th><th align="center" class="Rrule">LIVTENCITY<br/> N=234<br/> n (%)</th><th align="center" class="Rrule">IAT<br/> N=116<br/> n (%)</th> </tr> </thead> <tbody> <tr class="First"> <td align="left" class="Lrule Rrule">Neutrophils (cells/µL)</td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule">  &lt;500</td><td align="center" class="Rrule">4 (2)</td><td align="center" class="Rrule">4 (3)</td> </tr> <tr> <td align="left" class="Lrule Rrule">  ≥500 to &lt;750</td><td align="center" class="Rrule">7 (3)</td><td align="center" class="Rrule">7 (6)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  ≥750 to &lt;1,000</td><td align="center" class="Rrule">10 (4)</td><td align="center" class="Rrule">6 (5)</td> </tr> <tr> <td align="left" class="Lrule Rrule">Hemoglobin (g/dL)</td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule">  &lt;6.5</td><td align="center" class="Rrule">3 (1)</td><td align="center" class="Rrule">1 (1)</td> </tr> <tr> <td align="left" class="Lrule Rrule">  ≥6.5 to &lt;8.0</td><td align="center" class="Rrule">34 (15)</td><td align="center" class="Rrule">23 (20)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  ≥8.0 to &lt;9.5</td><td align="center" class="Rrule">76 (32)</td><td align="center" class="Rrule">33 (28)</td> </tr> <tr> <td align="left" class="Lrule Rrule">Platelets (cells/µL)</td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule">  &lt;25,000</td><td align="center" class="Rrule">11 (5)</td><td align="center" class="Rrule">6 (5)</td> </tr> <tr> <td align="left" class="Lrule Rrule">  ≥25,000 to &lt;50,000</td><td align="center" class="Rrule">27 (12)</td><td align="center" class="Rrule">10 (9)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  ≥50,000 to &lt;100,000</td><td align="center" class="Rrule">41 (18)</td><td align="center" class="Rrule">20 (17)</td> </tr> <tr> <td align="left" class="Lrule Rrule">Creatinine (mg/dL)</td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr> <td align="left" class="Lrule Rrule">  &gt;2.5</td><td align="center" class="Rrule">16 (7)</td><td align="center" class="Rrule">12 (10)</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">  &gt;1.5 to ≤2.5</td><td align="center" class="Rrule">78 (33)</td><td align="center" class="Rrule">29 (25)</td> </tr> </tbody> </table></div>

LIVTENCITY is not recommended to be coadministered with valganciclovir/ganciclovir (vGCV/GCV). LIVTENCITY may antagonize the antiviral activity of ganciclovir and valganciclovir by inhibiting human CMV pUL97 kinase, which is required for activation/phosphorylation of ganciclovir and valganciclovir [see Warnings and Precautions (5.1) and Microbiology (12.4)].

Maribavir is a substrate of CYP3A4. Coadministration of LIVTENCITY with strong inducers of CYP3A4 is not recommended, except for selected anticonvulsants [see Dosage and Administration (2.2) and Drug Interactions (7.3)].

Maribavir is a weak inhibitor of CYP3A4, and an inhibitor of P-gp and breast cancer resistance protein (BCRP). Coadministration of LIVTENCITY with drugs that are sensitive substrates of CYP3A, P-gp and BCRP may result in a clinically relevant increase in plasma concentrations of these substrates (see Table 4). Table 4 provides a list of established or potentially clinically significant drug interactions, based on either clinical drug interaction studies or predicted interactions due to the expected magnitude of interaction and potential for serious adverse events or decrease in efficacy [see Warnings and Precautions (5.3) and Clinical Pharmacology (12.3)].

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 4: Established and Other Potentially Significant Drug Interactions<a class="Sup" href="#footnote-3" name="footnote-reference-3">*</a></span> </caption> <col align="left" valign="middle" width="30%"/> <col align="center" valign="middle" width="20%"/> <col align="left" valign="middle" width="50%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule">Concomitant Drug Class: Drug Name</th><th align="left" class="Rrule">Effect on Concentration</th><th align="left" class="Rrule">Clinical Comments</th> </tr> </thead> <tfoot> <tr class="First Last"> <td align="left" colspan="3">↓=decrease, ↑=increase.</td> </tr> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-3" name="footnote-3">*</a> </dt> <dd>This table is not all inclusive.</dd> <dt> <a href="#footnote-reference-4" name="footnote-4">†</a> </dt> <dd>The interaction between LIVTENCITY and the concomitant drug was evaluated in a clinical study <span class="Italics">[see <a href="#S12.3">Clinical Pharmacology (12.3)</a>]</span>.</dd> <dt> <a href="#footnote-reference-5" name="footnote-5">‡</a> </dt> <dd>Refer to the respective prescribing information.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule"><span class="Bold">Antiarrhythmics</span></td><td align="center" class="Rrule" colspan="2"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Digoxin<a class="Sup" href="#footnote-4" name="footnote-reference-4">†</a></td><td align="center" class="Rrule">↑ Digoxin</td><td align="left" class="Rrule">Use caution when LIVTENCITY and digoxin are coadministered. Monitor serum digoxin concentrations. The dose of digoxin may need to be reduced when coadministered with LIVTENCITY.<a class="Sup" href="#footnote-5" name="footnote-reference-5">‡</a></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Anticonvulsants</span></td><td align="center" class="Rrule" colspan="2"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Carbamazepine</td><td align="center" class="Rrule">↓ Maribavir</td><td align="left" class="Rrule">A dose adjustment of LIVTENCITY to 800 mg twice daily is recommended when coadministered with carbamazepine.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Phenobarbital</td><td align="center" class="Rrule">↓ Maribavir</td><td align="left" class="Rrule">A dose adjustment of LIVTENCITY to 1,200 mg twice daily is recommended when coadministration with phenobarbital.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Phenytoin</td><td align="center" class="Rrule">↓ Maribavir</td><td align="left" class="Rrule">A dose adjustment of LIVTENCITY to 1,200 mg twice daily is recommended when coadministration with phenytoin.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Antimycobacterials</span></td><td align="center" class="Rrule" colspan="2"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" valign="middle">  Rifabutin</td><td align="center" class="Rrule" valign="middle">↓ Maribavir</td><td align="left" class="Rrule">Coadministration of LIVTENCITY and rifabutin is not recommended due to potential for a decrease in efficacy of LIVTENCITY.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Rifampin<a class="Sup" href="#footnote-4">†</a></td><td align="center" class="Rrule">↓ Maribavir</td><td align="left" class="Rrule">Coadministration of LIVTENCITY and rifampin is not recommended due to potential for a decrease in efficacy of LIVTENCITY.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Herbal Products</span></td><td align="center" class="Rrule" colspan="2"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  St. John's wort</td><td align="center" class="Rrule">↓ Maribavir</td><td align="left" class="Rrule">Coadministration of LIVTENCITY and St. John's wort is not recommended due to potential for a decrease in efficacy of LIVTENCITY. </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">HMG-CoA Reductase Inhibitors</span></td><td align="center" class="Rrule" colspan="2"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Rosuvastatin<a class="Sup" href="#footnote-5">‡</a></td><td align="center" class="Rrule">↑ Rosuvastatin</td><td align="left" class="Rrule">The patient should be closely monitored for rosuvastatin-related events, especially the occurrence of myopathy and rhabdomyolysis.<a class="Sup" href="#footnote-5">‡</a></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Immunosuppressants</span></td><td align="center" class="Rrule" colspan="2"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Cyclosporine</td><td align="center" class="Rrule">↑ Cyclosporine</td><td align="left" class="Rrule">Frequently monitor cyclosporine levels throughout treatment with LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.<a class="Sup" href="#footnote-5">‡</a></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Everolimus</td><td align="center" class="Rrule">↑ Everolimus</td><td align="left" class="Rrule">Frequently monitor everolimus levels throughout treatment with LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.<a class="Sup" href="#footnote-5">‡</a></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Sirolimus</td><td align="center" class="Rrule">↑ Sirolimus</td><td align="left" class="Rrule">Frequently monitor sirolimus levels throughout treatment with LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.<a class="Sup" href="#footnote-5">‡</a></td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">  Tacrolimus<a class="Sup" href="#footnote-4">†</a></td><td align="center" class="Rrule">↑ Tacrolimus</td><td align="left" class="Rrule">Frequently monitor tacrolimus levels throughout treatment with LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.<a class="Sup" href="#footnote-5">‡</a></td> </tr> </tbody> </table></div>

No clinically significant interactions were observed in clinical drug-drug interaction studies of LIVTENCITY and ketoconazole, antacid, caffeine, warfarin, voriconazole, dextromethorphan, or midazolam [see Clinical Pharmacology (12.3)].

Risk Summary

No adequate human data are available to establish whether LIVTENCITY poses a risk to pregnancy outcomes. In animal reproduction studies, embryo-fetal survival was decreased in rats, but not in rabbits, at maribavir exposures less than those observed in humans at the recommended human dose (RHD) (see Data).

The background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.

Data

Animal Data

In a combined fertility and embryofetal development study, maribavir was administered to male and female rats at oral doses of 100, 200, or 400 mg/kg/day. Females were dosed for 15 consecutive days prior to pairing, throughout pairing, and up to gestation day (GD) 17, while males were dosed 29 days prior to mating and throughout mating. A decrease in the number of viable fetuses and increase in early resorptions and post-implantation losses were observed at ≥100 mg/kg/day (at exposures approximately half the human exposure at the RHD). Intermittent reduced body weight gain was observed in pregnant animals at ≥200 mg/kg/day. Maribavir had no effect on embryo-fetal growth or development at dose levels up to 400 mg/kg/day, at exposures similar to those observed in humans at the RHD.

No significant toxicological effects on embryo-fetal growth or development were observed in rabbits when maribavir was administered at oral doses up to 100 mg/kg/day from GD 8 to 20, at exposures approximately half the human exposure at the RHD.

In the pre-and post-natal developmental toxicity study, maribavir was administered to pregnant rats at oral doses of 50, 150, or 400 mg/kg/day from GD 7 to post-natal day (PND) 21. A delay in developmental milestones was observed, including pinna detachment at doses ≥150 mg/kg/day and eye opening and preputial separation associated with reduced bodyweight gain of the offspring at 400 mg/kg/day. In addition, decreased fetal survival and litter loss was observed due to maternal toxicity and poor maternal care, respectively, at doses ≥150 mg/kg/day. No effects were observed at 50 mg/kg/day (which is estimated to be less than the human exposure at the RHD). No effects on number of offspring, proportion of males, number of live pups, or survival to PND 4 were observed at any dose in the offspring born to the second generation.

Risk Summary

It is not known whether maribavir or its metabolites are present in human or animal milk, affect milk production, or have effects on the breastfed infant. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for LIVTENCITY and any potential adverse effects to the breast-fed child.

The recommended dosing regimen in pediatric patients 12 years of age and older and weighing at least 35 kg is the same as that in adults. Use of LIVTENCITY in this age group is based on the following:

The safety and effectiveness of LIVTENCITY have not been established in children younger than 12 years of age.

No dosage adjustment is required for patients over 65 years of age based on the results from population pharmacokinetics analysis [see Clinical Pharmacology (12.3)] and efficacy and safety data from the clinical studies. In the clinical Study 303, 54 patients aged 65 years and over were treated with LIVTENCITY. Safety, effectiveness, and pharmacokinetics were consistent between elderly patients (≥65 years) and younger patients (<65 years).

No dose adjustment of LIVTENCITY is needed for patients with mild, moderate, or severe renal impairment [see Clinical Pharmacology (12.3)]. Administration of LIVTENCITY in patients with end stage renal disease (ESRD), including patients on dialysis, has not been studied.

No dose adjustment of LIVTENCITY is needed for patients with mild (Child-Pugh Class A) or moderate (Child-Pugh Class B) hepatic impairment [see Clinical Pharmacology (12.3)]. Administration of LIVTENCITY in patients with severe hepatic impairment has not been studied.

There is no known specific antidote for LIVTENCITY. In case of overdose, it is recommended that the patient be monitored for adverse reactions and appropriate symptomatic treatment instituted. Due to the high plasma protein binding of LIVTENCITY, dialysis is unlikely to reduce plasma concentrations of LIVTENCITY significantly.

{ "type": "p", "children": [], "text": "There is no known specific antidote for LIVTENCITY. In case of overdose, it is recommended that the patient be monitored for adverse reactions and appropriate symptomatic treatment instituted. Due to the high plasma protein binding of LIVTENCITY, dialysis is unlikely to reduce plasma concentrations of LIVTENCITY significantly." }

LIVTENCITY tablets contain maribavir, a benzimidazole riboside CMV pUL97 protein kinase inhibitor. The chemical name of maribavir is 5,6-Dichloro-N-(1-methylethyl)-1-β-L-ribofuranosyl-1H-benzimidazol-2-amine and the structural formula is:

{ "type": "p", "children": [], "text": "LIVTENCITY tablets contain maribavir, a benzimidazole riboside CMV pUL97 protein kinase inhibitor. The chemical name of maribavir is 5,6-Dichloro-N-(1-methylethyl)-1-β-L-ribofuranosyl-1H-benzimidazol-2-amine and the structural formula is:" }

The molecular formula for maribavir is C15H19Cl2N3O4 and its molecular weight is 376.23.

{ "type": "p", "children": [], "text": "The molecular formula for maribavir is C15H19Cl2N3O4 and its molecular weight is 376.23." }

Each 200 mg tablet for oral administration contains 200 mg maribavir and the following inactive ingredients: FD&C Blue #1, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, sodium starch glycolate, titanium dioxide, and talc.

{ "type": "p", "children": [], "text": "Each 200 mg tablet for oral administration contains 200 mg maribavir and the following inactive ingredients: FD&C Blue #1, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, sodium starch glycolate, titanium dioxide, and talc." }

LIVTENCITY is an antiviral drug against human CMV [see Microbiology (12.4)].

Exposure-Response

In dose-ranging studies that evaluated doses of 400 mg twice daily and twice daily doses of two and three times the recommended dose, no exposure-response relationship was observed for viral load or probability of unquantifiable plasma CMV DNA.

In Phase 3 Trial 303 that evaluated a maribavir dose of 400 mg twice daily, increasing maribavir exposure was not associated with increased probability of confirmed plasma CMV DNA < LLOQ (lower limit of quantification) at Week 8.

Cardiac Electrophysiology

At three times the recommended dose (approximately twice the peak concentration observed following the recommended dose), LIVTENCITY does not prolong the QT interval to any clinically relevant extent.

LIVTENCITY pharmacological activity is due to the parent drug. Following oral administration, plasma maribavir exposure (Cmax and AUC) increased approximately dose-proportionally following a single dose of 50 to 1600 mg (0.125 to four times the recommended dose) and multiple doses up to 2400 mg per day (three times the recommended daily dose). Maribavir PK is time-independent. With twice-daily dosing, steady state is reached within 2 days, with mean accumulation ratios of Cmax and AUC ranging from 1.37 to 1.47.

The pharmacokinetic properties of maribavir following administration of LIVTENCITY are displayed in Table 5. The multiple-dose pharmacokinetic parameters are provided in Table 6.

<div class="scrollingtable"><table width="90%"> <caption> <span>Table 5: Pharmacokinetic Properties of Maribavir</span> </caption> <col align="left" valign="top" width="50%"/> <col align="left" valign="top" width="50%"/> <tfoot> <tr> <td align="left" colspan="2"> <dl class="Footnote"> <dt> <a href="#footnote-reference-6" name="footnote-6">*</a> </dt> <dd>When taken orally with a high fat, high caloric meal vs fasted, the AUC<span class="Sub">0‑∞</span> and C<span class="Sub">max</span> (geometric mean ratio [90% CI] of maribavir are 0.878 [0.843, 0.915] and 0.716 [0.671, 0.764], respectively.</dd> <dt> <a href="#footnote-reference-7" name="footnote-7">†</a> </dt> <dd> <span class="Italics">In vitro</span> studies have shown that maribavir is biotransformed into a major circulating inactive metabolite: VP 44469 (N-dealkylated metabolite), with a metabolic ratio of 0.15 - 0.20. Multiple UGT enzymes, namely UGT1A1, UGT1A3, UGT2B7, and possibly UGT1A9, are involved in the glucuronidation of maribavir in humans, however, the contribution of glucuronidation to the overall clearance of maribavir is low based on <span class="Italics">In vitro</span> data.</dd> <dt> <a href="#footnote-reference-8" name="footnote-8">‡</a> </dt> <dd>Dosing in mass balance study: single-dose administration of [<span class="Sup">14</span>C] maribavir oral solution 400 mg containing 200 nCi of total radioactivity.</dd> </dl> </td> </tr> </tfoot> <tbody class="Headless"> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">Absorption<a class="Sup" href="#footnote-6" name="footnote-reference-6">*</a></span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">T<span class="Sub">max</span> (h), median</td><td align="left" class="Rrule">1.0 to 3.0</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">Distribution</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Mean apparent steady-state volume of distribution (V<span class="Sub">ss</span>, L)</td><td align="left" class="Rrule">24.9</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">% bound to human plasma proteins </td><td align="left" class="Rrule">98.0 across the concentration range of 0.05-200 µg/mL</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Blood-to plasma ratio</td><td align="left" class="Rrule">1.37</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Bold">Elimination </span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Major route of elimination</td><td align="left" class="Rrule">Hepatic metabolism</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Half-life (t<span class="Sub">1/2</span>) in transplant patients (h), mean</td><td align="left" class="Rrule">4.32</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Oral clearance (CL/F) in transplant patients (L/h), mean</td><td align="left" class="Rrule">2.67</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="2"><span class="Italics">Metabolism</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Metabolic pathways<a class="Sup" href="#footnote-7" name="footnote-reference-7">†</a></td><td align="left" class="Rrule">CYP3A4 (major) and CYP1A2 (minor)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Italics">Excretion</span></td><td align="left" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">% of dose excreted as total <span class="Sup">14</span>C (unchanged drug) in urine<a class="Sup" href="#footnote-8" name="footnote-reference-8">‡</a></td><td align="left" class="Rrule">61 (&lt;2)</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">% of dose excreted as total <span class="Sup">14</span>C (unchanged drug) in feces<a class="Sup" href="#footnote-8">‡</a></td><td align="left" class="Rrule">14 (5.7)</td> </tr> </tbody> </table></div>

<div class="scrollingtable"><table width="90%"> <caption> <span>Table 6: Multiple-Dose Pharmacokinetic Parameters of Maribavir</span> </caption> <col align="center" valign="top" width="32%"/> <col align="center" valign="top" width="34%"/> <col align="center" valign="top" width="34%"/> <thead> <tr class="Botrule First"> <th align="center" class="Lrule Rrule" colspan="3"> Geometric Mean (% CV)<a class="Sup" href="#footnote-9" name="footnote-reference-9">*</a></th> </tr> <tr class="Last"> <th align="center" class="Lrule Rrule">AUC<span class="Sub">0-tau</span><a class="Sup" href="#footnote-10" name="footnote-reference-10">†</a> <br/> (µg∙h/mL)</th><th align="center" class="Rrule">C<span class="Sub">max</span> <br/> (µg/mL)</th><th align="center" class="Rrule">C<span class="Sub">tau</span> <br/> (µg/mL)</th> </tr> </thead> <tfoot> <tr class="First Last"> <td align="left" colspan="3">CV=Coefficient of Variation; C<span class="Sub">max</span>=Maximum concentration; AUC<span class="Sub">0-tau</span>=Area under the time concentration curve over a dosing interval; C<span class="Sub">tau</span>=Concentration at the end of a dosing interval.</td> </tr> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-9" name="footnote-9">*</a> </dt> <dd>Pharmacokinetic parameter values based on post-hoc estimates from maribavir population pharmacokinetic model in transplant patients with CMV receiving 400 mg of LIVTENCITY twice daily with or without food.</dd> <dt> <a href="#footnote-reference-10" name="footnote-10">†</a> </dt> <dd>tau is maribavir dosing interval: 12 hours.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="First Last"> <td align="center" class="Lrule Rrule">142 (48.5%)</td><td align="center" class="Rrule">20.1 (35.5%)</td><td align="center" class="Rrule">5.43 (85.9%)</td> </tr> </tbody> </table></div>

Specific Populations

There were no clinically significant differences in the pharmacokinetics of maribavir based on age (18-79 years), gender, race (Caucasian, Black, Asian, or others), ethnicity (Hispanic/Latino or non-Hispanic/Latino), body weight (36 to 141 kg), transplant type, mild to severe renal impairment (measured creatinine clearance ranging from 12 to 70 mL/min), or mild to moderate hepatic impairment (Child-Pugh Class A or B).

Pediatric Patients

The pharmacokinetics of maribavir in patients less than 18 years of age have not been evaluated.

Using modeling and simulation, the recommended dosing regimen is expected to result in comparable steady-state plasma exposures of maribavir in patients 12 years of age and older and weighing at least 35 kg as observed in adults [see Use in Specific Populations (8.4)].

Drug Interactions

Based on in vitro studies, the metabolism of maribavir is not mediated by CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP3A5, UGT1A4, UGT1A6, UGT1A10, or UGT2B15. The transport of maribavir is not mediated by organic anion transporting polypeptide (OATP)1B1, OATP1B3, or bile salt export pump (BSEP).

At clinically relevant concentrations, clinically significant interactions are not expected when LIVTENCITY is coadministered with substrates of CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2E1, CYP2D6, CYP3A4; uridine diphosphate-glucuronosyltransferase (UGT)1A1, UGT1A4, UGT1A6, UGT1A9, UGT2B7; P-gp; BSEP; multidrug and toxin extrusion protein (MATE)1/2K; organic anion transporters (OAT)1 and OAT3; organic cation transporters (OCT)1 and OCT2; OATP1B1 and OATP1B3. In a clinical drug-drug interaction cocktail study, coadministration with maribavir had no effect on substrates of CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A4.

Drug interaction studies were performed with LIVTENCITY and other drugs likely to be coadministered for pharmacokinetic interactions. The effects of coadministration of other drugs on the pharmacokinetics of maribavir are summarized in Table 7, and the effects of maribavir on the pharmacokinetics of coadministered drugs are summarized in Table 8.

Dosing recommendations as a result of established and other potentially significant drug-drug interactions with LIVTENCITY are provided in Table 4 [see Drug Interactions (7.3)].

<div class="scrollingtable"><table width="90%"> <caption> <span>Table 7: Changes in Pharmacokinetics of LIVTENCITY in the Presence of Coadministered Drugs</span> </caption> <col align="center" valign="top" width="20%"/> <col align="center" valign="top" width="15%"/> <col align="center" valign="top" width="20%"/> <col align="center" valign="top" width="6%"/> <col align="center" valign="top" width="13%"/> <col align="center" valign="top" width="13%"/> <col align="center" valign="top" width="13%"/> <thead> <tr class="First"> <th align="center" class="Lrule Rrule" colspan="2" rowspan="2" valign="middle">Coadministered Drug and Regimen</th><th align="center" class="Rrule" rowspan="2" valign="middle">LIVTENCITY Regimen</th><th align="center" class="Rrule" rowspan="2" valign="middle">N</th><th align="center" class="Botrule Rrule" colspan="3">Geometric Mean Ratio (90% CI) of LIVTENCITY PK with/without Coadministered Drug<br/> [No Effect=1.00]</th> </tr> <tr class="Last"> <th align="center" class="Rrule">AUC</th><th align="center" class="Rrule">C<span class="Sub">max</span></th><th align="center" class="Rrule">C<span class="Sub">tau</span><a class="Sup" href="#footnote-11" name="footnote-reference-11">*</a></th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="7"> <dl class="Footnote"> <dt> <a href="#footnote-reference-11" name="footnote-11">*</a> </dt> <dd>tau is maribavir dosing interval: 12 hours.</dd> <dt> <a href="#footnote-reference-12" name="footnote-12">†</a> </dt> <dd>Based on physiologically based pharmacokinetic modeling results from 10 trials of 20 subjects each. The maribavir dosing regimen and geometric mean ratios (5<span class="Sup">th</span> percentile, 95<span class="Sup">th</span> percentile) correspond to dose-adjusted maribavir with inducer vs 400 mg twice daily without inducer.</dd> <dt> <a href="#footnote-reference-13" name="footnote-13">‡</a> </dt> <dd>Containing 800 mg aluminum hydroxide and 800 mg magnesium hydroxide.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="7"><span class="Bold">Anticonvulsants</span></td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">Carbamazepine<a class="Sup" href="#footnote-12" name="footnote-reference-12">†</a></td><td align="center" class="Rrule">400 mg once daily</td><td align="center" class="Rrule">800 mg twice daily / 400 mg twice daily</td><td align="center" class="Rrule">200</td><td align="center" class="Rrule">1.40<br/> (1.09, 1.67)</td><td align="center" class="Rrule">1.53<br/> (1.22, 1.79)</td><td align="center" class="Rrule">1.05<br/> (0.71, 1.40)</td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">Phenobarbital<a class="Sup" href="#footnote-12">†</a></td><td align="center" class="Rrule">100 mg once daily</td><td align="center" class="Rrule">1,200 mg twice daily / 400 mg twice daily</td><td align="center" class="Rrule">200</td><td align="center" class="Rrule" valign="middle">1.80<br/> (1.18, 2.35)</td><td align="center" class="Rrule" valign="middle">2.17<br/> (1.69, 2.57)</td><td align="center" class="Rrule" valign="middle">0.94<br/> (0.22, 1.97)</td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">Phenytoin<a class="Sup" href="#footnote-12">†</a></td><td align="center" class="Rrule">300 mg once daily</td><td align="center" class="Rrule">1,200 mg twice daily / 400 mg twice daily</td><td align="center" class="Rrule">200</td><td align="center" class="Rrule">1.70<br/> (1.06, 2.46)</td><td align="center" class="Rrule">2.05<br/> (1.49, 2.63)</td><td align="center" class="Rrule">0.89<br/> (0.26, 2.04)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="7"><span class="Bold">Antimycobacterials</span></td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">Rifampin</td><td align="center" class="Rrule">600 mg once daily</td><td align="center" class="Rrule">400 mg twice daily</td><td align="center" class="Rrule">14</td><td align="center" class="Rrule">0.40<br/> (0.36, 0.44)</td><td align="center" class="Rrule">0.61<br/> (0.52, 0.72)</td><td align="center" class="Rrule">0.18<br/> (0.14, 0.25)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="7"><span class="Bold">Antifungals</span></td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">Ketoconazole</td><td align="center" class="Rrule">400 mg single dose</td><td align="center" class="Rrule">400 mg single dose</td><td align="center" class="Rrule">19</td><td align="center" class="Rrule">1.53<br/> (1.44, 1.63)</td><td align="center" class="Rrule">1.10<br/> (1.01, 1.19)</td><td align="center" class="Rrule">-</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="7"><span class="Bold">Antacids</span></td> </tr> <tr class="Last"> <td align="center" class="Lrule Rrule">Aluminum hydroxide and magnesium hydroxide antacid</td><td align="center" class="Rrule">20 mL<a class="Sup" href="#footnote-13" name="footnote-reference-13">‡</a> single dose</td><td align="center" class="Rrule">100 mg single dose</td><td align="center" class="Rrule">15</td><td align="center" class="Rrule">0.89<br/> (0.83, 0.96)</td><td align="center" class="Rrule">0.84<br/> (0.75, 0.94)</td><td align="center" class="Rrule">-</td> </tr> </tbody> </table></div>

<div class="scrollingtable"><table width="90%"> <caption> <span>Table 8: Drug Interactions: Changes in Pharmacokinetics for Coadministered Drug in the Presence of 400 mg Twice Daily LIVTENCITY</span> </caption> <col align="center" valign="top" width="20%"/> <col align="center" valign="top" width="39%"/> <col align="center" valign="top" width="5%"/> <col align="center" valign="top" width="12%"/> <col align="center" valign="top" width="12%"/> <col align="center" valign="top" width="12%"/> <thead> <tr class="Botrule First"> <th align="center" class="Lrule Rrule" colspan="2" rowspan="2" valign="middle">Coadministered Drug and Regimen</th><th align="center" class="Rrule" rowspan="2" valign="middle">N</th><th align="center" class="Botrule Rrule" colspan="3">Geometric Mean Ratio (90% CI) of Coadministered Drug PK with/without LIVTENCITY<br/> [No Effect=1.00]</th> </tr> <tr class="Last"> <th align="center" class="Rrule">AUC</th><th align="center" class="Rrule">C<span class="Sub">max</span></th><th align="center" class="Rrule">C<span class="Sub">tau</span></th> </tr> </thead> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">Immunosuppressants</span></td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">Tacrolimus</td><td align="center" class="Rrule">stable dose, twice daily (total daily dose: 0.5-16 mg)</td><td align="center" class="Rrule">20</td><td align="center" class="Rrule">1.51<br/> (1.39, 1.65)</td><td align="center" class="Rrule">1.38<br/> (1.20, 1.57)</td><td align="center" class="Rrule">1.57<br/> (1.41, 1.74)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="6"><span class="Bold">P-gp substrate</span></td> </tr> <tr class="Botrule Last"> <td align="center" class="Lrule Rrule">Digoxin</td><td align="center" class="Rrule">0.5 mg<br/> single dose</td><td align="center" class="Rrule">18</td><td align="center" class="Rrule">1.21<br/> (1.10, 1.32)</td><td align="center" class="Rrule">1.25<br/> (1.13, 1.38)</td><td align="center" class="Rrule">-</td> </tr> </tbody> </table></div>

Mechanism of Action

The antiviral activity of maribavir is mediated by competitive inhibition of the protein kinase activity of human CMV enzyme pUL97, which results in inhibition of the phosphorylation of proteins. Maribavir inhibited wild-type pUL97 protein kinase in a biochemical assay with an IC50 value of 0.003 µM. Maribavir and its 5'-mono- and 5'-triphosphate derivatives at 100 µM had no significant effect on the incorporation of deoxynucleoside triphosphates by human CMV DNA polymerase. At a concentration of 100 µM, neither maribavir nor its 5′-triphosphate derivative inhibited CMV DNA polymerase delta, however the 5′-monophosphate derivative inhibited incorporation by polymerase delta of all 4 natural dNTPs by approximately 55%.

Antiviral Activity

Maribavir inhibited human CMV replication in virus yield reduction, DNA hybridization, and plaque reduction assays in human lung fibroblast cell line (MRC-5), human embryonic kidney (HEK), and human foreskin fibroblast (MRHF) cells. The EC50 values ranged from 0.03 to 2.2 µM depending on the cell line and assay endpoint. The cell culture antiviral activity of maribavir has also been evaluated against CMV clinical isolates. The median EC50 values were 0.1 µM (n=10, range 0.03-0.13 µM) and 0.28 µM (n=10, range 0.12-0.56 µM) using DNA hybridization and plaque reduction assays, respectively. No significant difference in EC50 values across the four human CMV glycoprotein B genotypes (N=2, 1, 4, and 1 for gB1, gB2, gB3, and gB4, respectively) was seen.

Combination Antiviral Activity

When maribavir was tested in combination with other antiviral compounds, antagonism of the antiviral activity was seen in combination with ganciclovir. No antagonism was observed with cidofovir, foscarnet, letermovir and rapamycin at the drugs EC50 values. The pUL97 kinase activity inhibited by maribavir is necessary to activate valganciclovir/ganciclovir.

Treatment Effect in CMV Glycoprotein B (gB) Subtypes

In Trial 303, the primary endpoint response rates for LIVTENCITY across CMV gB subtypes 1, 2, 3, 4, and 5 were 65% (55/85), 39% (22/57), 54% (22/41), 67% (14/21), and 64% (7/11), respectively. The primary endpoint response rates for IAT across CMV gB subtypes 1, 2, 3, 4, and 5 were 28% (15/53), 27% (4/15), 11% (2/19), 20% (2/10), and 17% (1/6), respectively [see Clinical Studies (14)].

Viral Resistance

In Cell Culture

Selection of maribavir resistant virus in cell culture and genotypic plus phenotypic characterization of these has identified amino acid substitutions that confer reduced susceptibility to maribavir. Substitutions identified in pUL97 include L337M, V353A, L397R, T409M, and H411L/N/Y. These substitutions confer reductions in susceptibility that range from 3.5-fold to >200-fold. Substitutions were also identified in pUL27:R233S, W362R, W153R, L193F, A269T, V353E, L426F, E22stop, W362stop, 218delC, and 301-311del. These substitutions confer reductions in susceptibility that range from 1.7- to 4.8-fold.

In Clinical Studies

In Phase 2 Study 202 evaluating maribavir in 120 hematopoietic stem cell transplant (HSCT) or solid organ transplant (SOT) recipients with phenotypic resistance to valganciclovir/ganciclovir, DNA sequence analysis of a select region of pUL97 (amino acids 270 to 482) and pUL27 (amino acids 108 to 424) was performed on 34 paired virologic failure samples. There were 25 patients with treatment-emergent maribavir resistance-associated substitution(s) in pUL97 F342Y (4.5-fold reduction in susceptibility), T409M (78-fold reduction), H411L/Y (69- and 12-fold reduction) and/or C480F (224-fold reduction).

In Phase 3 Study 303 evaluating maribavir in patients with phenotypic resistance to valganciclovir/ganciclovir, DNA sequence analysis of the entire coding regions of pUL97 and pUL27 was performed on 134 paired sequences from maribavir-treated patients. The treatment-emergent pUL97 substitutions F342Y (4.5-fold), T409M (78-fold), H411L/N/Y (69-, 9-, and 12-fold, respectively), and/or C480F (224-fold) were detected in 58 subjects (47 subjects were on-treatment failures and 11 subjects were relapsers). One subject with the pUL27 L193F substitution (2.6-fold reduced susceptibility to maribavir) at baseline did not meet the primary endpoint.

Cross-Resistance

Cross-resistance has been observed between maribavir and ganciclovir/valganciclovir in cell culture and in clinical studies.

pUL97 valganciclovir/ganciclovir resistance-associated substitutions F342S/Y, K355del, V356G, D456N, V466G, C480R, P521L, and Y617del reduce susceptibility to maribavir >4.5-fold. Other vGCV/GCV resistance pathways have not been evaluated for cross-resistance to maribavir. pUL54 DNA polymerase substitutions conferring resistance to vGCV/GCV, cidofovir, or foscarnet remained susceptible to maribavir.

Substitutions pUL97 F342Y and C480F are maribavir treatment-emergent resistance-associated substitutions that confer >1.5-fold reduced susceptibility to vGCV/GCV, a fold reduction that is associated with phenotypic resistance to vGCV/GCV. The clinical significance of this cross-resistance to vGCV/GCV for these substitutions has not been determined. Maribavir resistant virus remained susceptible to cidofovir and foscarnet. Additionally, there are no reports of any pUL27 maribavir resistance-associated substitutions being evaluated for vGCV/GCV, cidofovir, or foscarnet cross-resistance. Given the lack of resistance-associated substitutions for these drugs mapping to pUL27, cross-resistance is not expected for pUL27 maribavir substitutions.

Two-year carcinogenicity studies were conducted in mice and rats administered oral doses up to 150 and 100 mg/kg/day, respectively. Maribavir was not carcinogenic in rats at any dose tested, corresponding to maribavir exposures less than human exposure at the RHD. At 150 mg/kg/day in male mice only, an increased incidence of hemangioma, hemangiosarcoma, and combined hemangioma/hemangiosarcoma was observed across multiple tissues, at exposures less than the human exposure at the RHD. There were no carcinogenic findings in male mice at ≤75 mg/kg/day and female mice at any dose.

Mutagenicity

Maribavir was negative in a bacterial mutation assay and the in vivo rat bone marrow micronucleus assay. Maribavir was positive in the absence of metabolic activation in the mouse lymphoma assay, and the results were equivocal in the presence of metabolic activation.

Impairment of Fertility

Although decreased sperm straight line velocity was observed in males (at maribavir exposures less than those observed in humans at the RHD), there were no effects on fertility in males or females in a combined oral fertility and embryo-fetal study in rats administered maribavir at up to 400 mg/kg/day [see Use in Specific Populations (8.1)].

LIVTENCITY was evaluated in a Phase 3, multicenter, randomized, open-label, active-controlled superiority trial (NCT02931539, Trial 303) to assess the efficacy and safety of LIVTENCITY compared to Investigator-Assigned Treatment (IAT) (ganciclovir, valganciclovir, foscarnet, or cidofovir) in 352 HSCT or SOT recipients with CMV infections that were refractory to treatment with ganciclovir, valganciclovir, foscarnet, or cidofovir, including CMV infections with or without confirmed resistance to 1 or more of the IATs. Subjects with CMV disease involving the central nervous system, including the retina, were excluded from the study.

Subjects were stratified by transplant type (HSCT or SOT) and screening CMV DNA levels and then randomized in a 2:1 allocation ratio to receive either LIVTENCITY 400 mg twice daily or IAT as dosed by the investigator for up to 8 weeks. After completion of the treatment period, subjects entered a 12-week follow-up phase.

The mean age of trial subjects was 53 years and most subjects were male (61%), white (76%) and not Hispanic or Latino (83%), with similar distributions across the two treatment arms. The most common treatment used in the IAT arm was foscarnet which was administered in 47 (41%) subjects followed by ganciclovir or valganciclovir, each administered in 28 (24%) subjects. Cidofovir was administered in 6 subjects, the combination of foscarnet and valganciclovir in 4 subjects and the combination of foscarnet and ganciclovir in 3 subjects. Baseline disease characteristics are summarized in Table 9 below.

<div class="scrollingtable"><table width="85%"> <caption> <span>Table 9: Summary of Baseline Disease Characteristics in Trial 303</span> </caption> <col align="left" valign="top" width="50%"/> <col align="center" valign="top" width="25%"/> <col align="center" valign="top" width="25%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule" rowspan="2" valign="middle">Characteristic</th><th align="center" class="Rrule" valign="bottom">LIVTENCITY<br/> 400 mg Twice Daily<br/>N=235<br/> n (%)</th><th align="center" class="Rrule" valign="bottom">IAT<br/>N=117<br/> n (%)</th> </tr> </thead> <tfoot> <tr class="First Last"> <td align="left" colspan="3">CMV=cytomegalovirus, DNA=deoxyribonucleic acid, HSCT=hematopoietic stem cell transplant, IAT=investigator assigned anti-CMV treatment, N=number of patients, SOT=solid organ transplant.</td> </tr> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-14" name="footnote-14">*</a> </dt> <dd>one of the subjects had both CMV syndrome and disease but was counted for CMV disease only.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule"><span class="Bold">Transplant type</span></td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  HSCT</td><td align="center" class="Rrule">93 (40)</td><td align="center" class="Rrule">48 (41)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  SOT</td><td align="center" class="Rrule">142 (60)</td><td align="center" class="Rrule">69 (59)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    Kidney</td><td align="center" class="Rrule">74 (52)</td><td align="center" class="Rrule">32 (46)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    Lung</td><td align="center" class="Rrule">40 (28)</td><td align="center" class="Rrule">22 (32)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    Heart</td><td align="center" class="Rrule">14 (10)</td><td align="center" class="Rrule">9 (13)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    Other (multiple, liver, pancreas, intestine)</td><td align="center" class="Rrule">14 (10)</td><td align="center" class="Rrule">6 (9)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">CMV DNA levels</span></td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Low (&lt;9,100 IU/mL)</td><td align="center" class="Rrule">153 (65)</td><td align="center" class="Rrule">85 (73)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Intermediate (≥9,100 to &lt;91,000 IU/mL)</td><td align="center" class="Rrule">68 (29)</td><td align="center" class="Rrule">25 (21)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  High (≥91,000 IU/mL)</td><td align="center" class="Rrule">14 (6)</td><td align="center" class="Rrule">7 (6)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule"><span class="Bold">Confirmed symptomatic CMV infection at baseline</span></td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  No</td><td align="center" class="Rrule">214 (91)</td><td align="center" class="Rrule">109 (93)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Yes<a class="Sup" href="#footnote-14" name="footnote-reference-14">*</a></td><td align="center" class="Rrule">21 (9)</td><td align="center" class="Rrule">8 (7)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    CMV syndrome (SOT only)</td><td align="center" class="Rrule">9 (43)</td><td align="center" class="Rrule">7 (88)</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">    Tissue Invasive disease</td><td align="center" class="Rrule">12 (57)<a class="Sup" href="#footnote-14">*</a></td><td align="center" class="Rrule">1 (13)</td> </tr> </tbody> </table></div>

Primary Efficacy Endpoint

The primary efficacy endpoint was confirmed CMV DNA level < LLOQ (i.e;, <137 IU/mL) as assessed by COBAS® AmpliPrep/COBAS® TaqMan® CMV test) at the end of Week 8. The key secondary endpoint was CMV DNA level < LLOQ and CMV infection symptom control at the end of Study Week 8 with maintenance of this treatment effect through Study Week 16.

For the primary endpoint, LIVTENCITY was statistically superior to IAT (56% vs 24%, respectively), as shown in Table 10.

<div class="scrollingtable"><table width="80%"> <caption> <span>Table 10: Primary Efficacy Endpoint Analysis at Week 8 (Randomized Set) in Trial 303</span> </caption> <col align="left" valign="top" width="55%"/> <col align="center" valign="top" width="15%"/> <col align="center" valign="top" width="30%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule">LIVTENCITY<br/>400 mg<br/>Twice Daily<br/>N=235<br/> n (%)</th><th align="center" class="Rrule" valign="middle">IAT<br/>N=117<br/> n (%)</th> </tr> </thead> <tfoot> <tr class="First Last"> <td align="left" colspan="3">CI=confidence interval; CMV=cytomegalovirus; IAT=investigator-assigned anti-CMV treatment; N=number of patients.</td> </tr> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-15" name="footnote-15">*</a> </dt> <dd>Confirmed CMV DNA level &lt; LLOQ at the end of Week 8 (2 consecutive samples separated by at least 5 days with DNA levels &lt; LLOQ [i.e:, &lt;137 IU/mL]).</dd> <dt> <a href="#footnote-reference-16" name="footnote-16">†</a> </dt> <dd>Cochran-Mantel-Haenszel weighted average approach was used for the adjusted difference in proportion (maribavir – IAT), the corresponding 95% CI, and the p-value after adjusting for the transplant type and baseline plasma CMV DNA concentration. Only those with both stratification factors were included in the computation.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule"><span class="Bold">Primary Endpoint: Confirmed CMV DNA Level &lt; LLOQ at Week 8<a class="Sup" href="#footnote-15" name="footnote-reference-15">*</a></span></td><td align="center" class="Rrule"></td><td align="center" class="Rrule"></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Responders</td><td align="center" class="Rrule">131 (56)</td><td align="center" class="Rrule">28 (24)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Adjusted difference in proportion of responders (95% CI)<a class="Sup" href="#footnote-16" name="footnote-reference-16">†</a></td><td align="center" class="Rrule">33 (23, 43)</td><td align="center" class="Rrule"></td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">p-value: adjusted<a class="Sup" href="#footnote-16">†</a></td><td align="center" class="Rrule">&lt;0.001</td><td align="center" class="Rrule"></td> </tr> </tbody> </table></div>

The reasons for failure to meet the primary endpoint are summarized in Table 11.

<div class="scrollingtable"><table width="75%"> <caption> <span>Table 11: Analysis of Failures for Primary Efficacy Endpoint</span> </caption> <col align="left" valign="top" width="50%"/> <col align="center" valign="top" width="25%"/> <col align="center" valign="top" width="25%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule" valign="top">Outcome at Week 8</th><th align="center" class="Rrule" valign="top">LIVTENCITY<br/> N=235<br/> n (%)</th><th align="center" class="Rrule" valign="top">IAT<br/> N=117<br/> n (%)</th> </tr> </thead> <tfoot> <tr class="First"> <td align="left" colspan="3">CMV=Cytomegalovirus, IAT=Investigator-assigned anti-CMV Treatment, MBV=maribavir.</td> </tr> <tr class="Last"> <td align="left" colspan="3">Percentages are based on the number of subjects in the Randomized Set.</td> </tr> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-17" name="footnote-17">*</a> </dt> <dd>Confirmed CMV DNA level &lt; LLOQ at the end of Week 8 (2 consecutive samples separated by at least 5 days with DNA levels &lt; LLOQ [i.e:, &lt;137 IU/mL]).</dd> <dt> <a href="#footnote-reference-18" name="footnote-18">†</a> </dt> <dd>CMV DNA breakthrough=achieved confirmed CMV DNA level &lt; LLOQ and subsequently became detectable.</dd> <dt> <a href="#footnote-reference-19" name="footnote-19">‡</a> </dt> <dd>Other reasons=other reasons not including adverse events, deaths and lack of efficacy, withdrawal of consent, and non-compliance.</dd> <dt> <a href="#footnote-reference-20" name="footnote-20">§</a> </dt> <dd>Includes subjects who completed study assigned treatment and were non-responders.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" valign="top"><span class="Bold">Responders (Confirmed DNA Level &lt; LLOQ)<a class="Sup" href="#footnote-17" name="footnote-reference-17">*</a></span></td><td align="center" class="Rrule" valign="top"><span class="Bold">131 (56)</span></td><td align="center" class="Rrule" valign="top"><span class="Bold">28 (24)</span></td> </tr> <tr> <td align="left" class="Lrule Rrule"><span class="Bold">Non-responders:</span></td><td align="center" class="Rrule"><span class="Bold">104 (44)</span></td><td align="center" class="Rrule"><span class="Bold">89 (76)</span></td> </tr> <tr> <td align="left" class="Lrule Rrule">  <span class="Bold">Due to virologic failure<a class="Sup" href="#footnote-18" name="footnote-reference-18">†</a>:</span></td><td align="center" class="Rrule"><span class="Bold">80 (34)</span></td><td align="center" class="Rrule"><span class="Bold">42 (36)</span></td> </tr> <tr> <td align="left" class="Lrule Rrule">     •  CMV DNA never &lt; LLOQ</td><td align="center" class="Rrule">48 (20)</td><td align="center" class="Rrule">35 (30)</td> </tr> <tr> <td align="left" class="Lrule Rrule">     •  CMV DNA breakthrough<a class="Sup" href="#footnote-18">†</a></td><td align="center" class="Rrule">32 (14)</td><td align="center" class="Rrule">7 (6)</td> </tr> <tr> <td align="left" class="Lrule Rrule">  <span class="Bold">Due to drug/study discontinuation:</span></td><td align="center" class="Rrule"><span class="Bold">21 (9)</span></td><td align="center" class="Rrule"><span class="Bold">44 (38)</span></td> </tr> <tr> <td align="left" class="Lrule Rrule">     •  Adverse events</td><td align="center" class="Rrule">8 (3)</td><td align="center" class="Rrule">26 (22)</td> </tr> <tr> <td align="left" class="Lrule Rrule">     •  Deaths</td><td align="center" class="Rrule">10 (4)</td><td align="center" class="Rrule">3 (3)</td> </tr> <tr> <td align="left" class="Lrule Rrule">    •  Withdrawal of consent</td><td align="center" class="Rrule">1 (&lt;1)</td><td align="center" class="Rrule">9 (8)</td> </tr> <tr> <td align="left" class="Lrule Rrule">     •  Other reasons<a class="Sup" href="#footnote-19" name="footnote-reference-19">‡</a></td><td align="center" class="Rrule">2 (1)</td><td align="center" class="Rrule">6 (5)</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">  <span class="Bold">Due to other reasons but remained on study<a class="Sup" href="#footnote-20" name="footnote-reference-20">§</a></span></td><td align="center" class="Rrule"><span class="Bold">3 (1)</span></td><td align="center" class="Rrule"><span class="Bold">3 (3)</span></td> </tr> </tbody> </table></div>

The treatment effect of LIVTENCITY was consistent across transplant type, age group, and the presence of CMV syndrome/disease at baseline. However, LIVTENCITY was less effective against subjects with increased CMV DNA levels (≥50,000 IU/mL) and subjects with absence of genotypic resistance (see Table 12).

<div class="scrollingtable"><table width="90%"> <caption> <span>Table 12: Responders by Subgroup in Trial 303</span> </caption> <col align="left" valign="middle" width="40%"/> <col align="center" valign="middle" width="15%"/> <col align="center" valign="middle" width="15%"/> <col align="center" valign="middle" width="15%"/> <col align="center" valign="middle" width="15%"/> <thead> <tr class="Botrule First"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule" colspan="2">LIVTENCITY 400 mg<br/>Twice Daily<br/>N=235</th><th align="center" class="Rrule" colspan="2" valign="bottom">IAT<br/>N=117</th> </tr> <tr class="Last"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule">n/N</th><th align="center" class="Rrule">%</th><th align="center" class="Rrule">n/N</th><th align="center" class="Rrule">%</th> </tr> </thead> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Transplant type</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  SOT</td><td align="center" class="Rrule">79/142</td><td align="center" class="Rrule">56</td><td align="center" class="Rrule">18/69</td><td align="center" class="Rrule">26</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  HSCT</td><td align="center" class="Rrule">52/93</td><td align="center" class="Rrule">56</td><td align="center" class="Rrule">10/48</td><td align="center" class="Rrule">21</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Baseline CMV DNA viral load</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Low (&lt;9,100 IU/mL)</td><td align="center" class="Rrule">95/153</td><td align="center" class="Rrule">62</td><td align="center" class="Rrule">21/85</td><td align="center" class="Rrule">25</td> </tr> <tr> <td align="left" class="Lrule Rrule">  Intermediate (≥9,100 to &lt;91,000 IU/mL)</td><td align="center" class="Rrule">32/68</td><td align="center" class="Rrule">47</td><td align="center" class="Rrule">5/25</td><td align="center" class="Rrule">20</td> </tr> <tr> <td align="left" class="Lrule Rrule">    ≥9,100 to &lt;50,000 IU/mL</td><td align="center" class="Rrule">29/59</td><td align="center" class="Rrule">49</td><td align="center" class="Rrule">4/20</td><td align="center" class="Rrule">20</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">    ≥50,000 to &lt;91,000 IU/mL</td><td align="center" class="Rrule">3/9</td><td align="center" class="Rrule">33</td><td align="center" class="Rrule">1/5</td><td align="center" class="Rrule">20</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  High (≥91,000 IU/mL)</td><td align="center" class="Rrule">4/14</td><td align="center" class="Rrule">29</td><td align="center" class="Rrule">2/7</td><td align="center" class="Rrule">29</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Genotypic resistance to other anti-CMV agents</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Yes</td><td align="center" class="Rrule">76/121</td><td align="center" class="Rrule">63</td><td align="center" class="Rrule">14/69</td><td align="center" class="Rrule">20</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  No</td><td align="center" class="Rrule">42/96</td><td align="center" class="Rrule">44</td><td align="center" class="Rrule">11/34</td><td align="center" class="Rrule">32</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">CMV syndrome/disease at baseline</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  Yes</td><td align="center" class="Rrule">10/21</td><td align="center" class="Rrule">48</td><td align="center" class="Rrule">1/8</td><td align="center" class="Rrule">13</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  No</td><td align="center" class="Rrule">121/214</td><td align="center" class="Rrule">57</td><td align="center" class="Rrule">27/109</td><td align="center" class="Rrule">25</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="5"><span class="Bold">Age Group</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  18 to 44 years</td><td align="center" class="Rrule">28/55</td><td align="center" class="Rrule">51</td><td align="center" class="Rrule">8/32</td><td align="center" class="Rrule">25</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">  45 to 64 years</td><td align="center" class="Rrule">71/126</td><td align="center" class="Rrule">56</td><td align="center" class="Rrule">19/69</td><td align="center" class="Rrule">28</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">  ≥65 years</td><td align="center" class="Rrule">32/54</td><td align="center" class="Rrule">59</td><td align="center" class="Rrule">1/16</td><td align="center" class="Rrule">6</td> </tr> </tbody> </table></div>

Secondary Endpoints

Table 13 shows results of the secondary endpoint, achievement of CMV DNA level < LLOQ and symptom controla at Week 8 with maintenance through Week 16.

<div class="scrollingtable"><table width="90%"> <caption> <span>Table 13: Achievement of CMV DNA Level &lt; LLOQ and CMV Infection Symptom Control at Week 8, With Maintenance Through Week 16<a class="Sup" href="#footnote-21" name="footnote-reference-21">*</a></span> </caption> <col align="left" valign="top" width="60%"/> <col align="center" valign="top" width="20%"/> <col align="center" valign="top" width="20%"/> <thead> <tr class="First Last"> <th align="left" class="Lrule Rrule"></th><th align="center" class="Rrule">LIVTENCITY<br/> 400 mg<br/>Twice Daily<br/> N=235<br/> n (%)</th><th align="center" class="Rrule" valign="middle">IAT<br/>N=117<br/> n (%)</th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="3"> <dl class="Footnote"> <dt> <a href="#footnote-reference-21" name="footnote-21">*</a> </dt> <dd>CMV infection symptom control was defined as resolution or improvement of tissue-invasive disease or CMV syndrome for symptomatic patients at baseline, or no new symptoms for patients who were asymptomatic at baseline.</dd> <dt> <a href="#footnote-reference-22" name="footnote-22">†</a> </dt> <dd>Cochran-Mantel-Haenszel weighted average approach was used for the adjusted difference in proportion (maribavir – IAT), the corresponding 95% CI, and the p-value after adjusting for the transplant type and baseline plasma CMV DNA concentration. Only those with both stratification factors were included in the computation.</dd> </dl> </td> </tr> </tfoot> <tbody> <tr class="Botrule First"> <td align="left" class="Lrule Rrule">Responders</td><td align="center" class="Rrule">44 (19)</td><td align="center" class="Rrule">12 (10)</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule">Adjusted difference in proportion of responders (95% CI)<a class="Sup" href="#footnote-22" name="footnote-reference-22">†</a></td><td align="center" class="Rrule">9 (2,17)</td><td align="center" class="Rrule"></td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule">p-value: adjusted<a class="Sup" href="#footnote-22">†</a></td><td align="center" class="Rrule">0.013</td><td align="center" class="Rrule"></td> </tr> </tbody> </table></div>

Virologic relapse during follow-up period: After the end of treatment phase, 65/131 (50%) of subjects in the LIVTENCITY group and 11/28 (39%) subjects in the IAT group who achieved CMV DNA level < LLOQ experienced virologic relapse during the follow-up period. Most of the relapses 58/65 (89%) in LIVTENCITY group and 11/11 (100% in IAT group)] occurred within 4 weeks after study drug discontinuation; and the median time to relapse after CMV DNA level < LLOQ was 15 days (range 7, 71) in the LIVTENCITY group and 15 days (range 7, 29) in the IAT group [see Warnings and Precautions (5.2) and Microbiology (12.4)].

New onset symptomatic CMV infection: For the entire study period, a similar percentage of subjects in each treatment group developed new onset symptomatic CMV infection (LIVTENCITY 6% [14/235]; IAT 6% [7/113]).

Overall mortality: All-cause mortality was assessed for the entire study period. A similar percentage of subjects in each treatment group died during the trial (LIVTENCITY 11% [27/235]; IAT 11% [13/117]).

Storage and Handling

Store at 20°C to 25°C (68°F to 77°F), brief exposure to 15°C to 30°C (59°F to 86°F) permitted [see USP Controlled Room Temperature].

Advise the patient to read the FDA-approved patient labeling (Patient Information and Instructions for Use).

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Inform patients that LIVTENCITY may interact with other drugs. Advise patients to report to their healthcare provider the use of any other medication [see Warnings and Precautions (5.1 and 5.3), Drug Interactions (7)].

{ "type": "p", "children": [], "text": "Inform patients that LIVTENCITY may interact with other drugs. Advise patients to report to their healthcare provider the use of any other medication [see Warnings and Precautions (5.1 and 5.3), Drug Interactions (7)]. \t\t\t\t\t\t" }

Distributed by: Takeda Pharmaceuticals America, Inc. Lexington, MA 02421

{ "type": "p", "children": [], "text": "Distributed by:\nTakeda Pharmaceuticals America, Inc.\n Lexington, MA 02421" }

LIVTENCITY® and the LIVTENCITY Logo® are registered trademarks of Takeda Pharmaceuticals International AG.

{ "type": "p", "children": [], "text": "LIVTENCITY® and the LIVTENCITY Logo® are registered trademarks of Takeda Pharmaceuticals International AG." }

TAKEDA® and the TAKEDA Logo® are registered trademarks of Takeda Pharmaceutical Company Limited.

{ "type": "p", "children": [], "text": "TAKEDA® and the TAKEDA Logo® are registered trademarks of Takeda Pharmaceutical Company Limited." }

©2024 Takeda Pharmaceuticals U.S.A., Inc. All rights reserved.

{ "type": "p", "children": [], "text": "©2024 Takeda Pharmaceuticals U.S.A., Inc. All rights reserved." }

MAR358 R4

{ "type": "p", "children": [], "text": "MAR358 R4" }

<div class="scrollingtable"><table width="100%"> <col align="left" valign="top" width="2%"/> <col align="left" valign="top" width="48%"/> <col align="left" valign="top" width="30%"/> <col align="right" valign="top" width="20%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule" colspan="4">Patient Information<br/> LIVTENCITY (liv-TEN-city)<br/> (maribavir)<br/> tablets</th> </tr> </thead> <tfoot> <tr class="First"> <td align="left" colspan="3">This Patient Information has been approved by the U.S. Food and Drug Administration.          MAR358 R4</td><td align="right">Revised: March 2024</td> </tr> <tr class="Last"> <td align="left"></td><td align="left"></td><td align="left"></td><td align="left"></td> </tr> </tfoot> <tbody> <tr class="First"> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">What is LIVTENCITY?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4">LIVTENCITY is a prescription medicine used to treat cytomegalovirus (CMV) infection and disease in adults and children 12 years of age and older weighing at least 77 pounds (35 kg) who have received a transplant, when their infection or disease does not respond to treatment with the medicines ganciclovir, valganciclovir, cidofovir or foscarnet.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="4">It is not known if LIVTENCITY is safe and effective in children under 12 years of age.</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">Before taking LIVTENCITY, tell your healthcare provider about all your medical conditions, including if you:</span> <ul class="Disc"> <li>are pregnant or plan to become pregnant. It is not known if LIVTENCITY will harm your unborn baby.</li> <li>are breastfeeding or plan to breastfeed. It is not known if LIVTENCITY passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby during treatment with LIVTENCITY.</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">Tell your healthcare provider about all of the medicines you take,</span> including prescription and over-the-counter medicines, vitamins and herbal supplements. LIVTENCITY may affect the way other medicines work, and other medicines may affect how LIVTENCITY works and cause serious side effects.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="4">Especially tell your healthcare provider if you take a seizure (anticonvulsant) medicine.<ul class="Disc"> <li>You can ask your healthcare provider or pharmacist for a list of medicines that interact with LIVTENCITY.</li> <li> <span class="Bold">Do not start a new medicine without telling your healthcare provider</span><span class="Bold">.</span> Your healthcare provider will tell you if it is safe to take LIVTENCITY with other medicines.</li> <li>Know the medicines you take. Keep a list of your medicines and show it to your healthcare provider and pharmacist when you get a new medicine.</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">How should I take LIVTENCITY?</span> <ul class="Disc"> <li>Take LIVTENCITY exactly as your healthcare provider tells you to take it.</li> <li>Take LIVTENCITY 2 times a day.</li> <li>Take LIVTENCITY with or without food.</li> <li>Swallow LIVTENCITY tablets whole. </li> <li>If you are not able to swallow tablets whole, you can break apart (disperse) the tablets in drinking water <span class="Bold">or</span> crush the tablets and mix with drinking water and take by mouth. <span class="Bold">See the "<a href="#IFU">Instructions for Use</a>" for detailed instructions</span> on how to prepare and give a dose of LIVTENCITY tablets by dispersing or crushing tablets and taking by mouth. </li> <li>If you have a Nasogastric (NG) or Orogastric (OG) Tube (French size 10 or larger), you can disperse the tablets and take through a NG or OG tube. <span class="Bold">See the "<a href="#IFU">Instructions for Use</a>" for detailed instructions</span> on how to prepare and give a dose of LIVTENCITY tablets through a NG or OG Tube. </li> <li>If you take too much LIVTENCITY, call your healthcare provider or go to the nearest hospital emergency room right away.</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">What are the possible side effects of LIVTENCITY?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">The most common side effects of LIVTENCITY include:</span></td> </tr> <tr> <td align="left" class="Lrule"></td><td align="left"> <ul class="Disc"> <li>changes in taste</li> <li>nausea</li> <li>diarrhea</li> </ul> </td><td align="left" class="Rrule" colspan="2"> <ul class="Disc"> <li>vomiting</li> <li>tiredness</li> </ul> </td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4">These are not all the possible side effects of LIVTENCITY.</td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="4">Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">How should I store LIVTENCITY?</span> <ul class="Disc"> <li>Store LIVTENCITY at room temperature between 68°F to 77°F (20°C to 25°C).</li> </ul> </td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">Keep LIVTENCITY and all medicines out of the reach of children.</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">General information about the safe and effective use of LIVTENCITY.</span></td> </tr> <tr class="Botrule"> <td align="left" class="Lrule Rrule" colspan="4">Medicines are sometimes prescribed for purposes other than those listed in the Patient Information leaflet. Do not use LIVTENCITY for a condition for which it was not prescribed. Do not give LIVTENCITY to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about LIVTENCITY that is written for health professionals.</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">What are the ingredients in LIVTENCITY?</span></td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">Active ingredient:</span> maribavir</td> </tr> <tr> <td align="left" class="Lrule Rrule" colspan="4"><span class="Bold">Inactive ingredients:</span> FD&amp;C Blue #1, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, sodium starch glycolate, titanium dioxide, and talc.</td> </tr> <tr class="Last"> <td align="left" class="Lrule Rrule" colspan="4">Distributed by: <span class="Bold">Takeda Pharmaceuticals America, Inc.,</span> Lexington, MA 02421<br/> LIVTENCITY<span class="Sup">®</span> and the LIVTENCITY Logo<span class="Sup">®</span> are registered trademarks of Takeda Pharmaceuticals International AG. TAKEDA<span class="Sup">®</span> and the TAKEDA Logo<span class="Sup">®</span> are registered trademarks of Takeda Pharmaceutical Company Limited. ©2024 Takeda Pharmaceuticals U.S.A., Inc. All rights reserved.<br/> For more information, go to <a href="http://www.explorelivtencity.com">www.explorelivtencity.com</a> or call 1-877-TAKEDA-7 (1-877-825-3327).</td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"100%\">\n<col align=\"left\" valign=\"top\" width=\"2%\"/>\n<col align=\"left\" valign=\"top\" width=\"48%\"/>\n<col align=\"left\" valign=\"top\" width=\"30%\"/>\n<col align=\"right\" valign=\"top\" width=\"20%\"/>\n<thead>\n<tr class=\"First Last\">\n<th align=\"center\" class=\"Lrule Rrule\" colspan=\"4\">Patient Information<br/> LIVTENCITY (liv-TEN-city)<br/> (maribavir)<br/> tablets</th>\n</tr>\n</thead>\n<tfoot>\n<tr class=\"First\">\n<td align=\"left\" colspan=\"3\">This Patient Information has been approved by the U.S. Food and Drug Administration.          MAR358 R4</td><td align=\"right\">Revised: March 2024</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\"></td><td align=\"left\"></td><td align=\"left\"></td><td align=\"left\"></td>\n</tr>\n</tfoot>\n<tbody>\n<tr class=\"First\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">What is LIVTENCITY?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">LIVTENCITY is a prescription medicine used to treat cytomegalovirus (CMV) infection and disease in adults and children 12 years of age and older weighing at least 77 pounds (35 kg) who have received a transplant, when their infection or disease does not respond to treatment with the medicines ganciclovir, valganciclovir, cidofovir or foscarnet.</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">It is not known if LIVTENCITY is safe and effective in children under 12 years of age.</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">Before taking LIVTENCITY, tell your healthcare provider about all your medical conditions, including if you:</span>\n<ul class=\"Disc\">\n<li>are pregnant or plan to become pregnant. It is not known if LIVTENCITY will harm your unborn baby.</li>\n<li>are breastfeeding or plan to breastfeed. It is not known if LIVTENCITY passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby during treatment with LIVTENCITY.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">Tell your healthcare provider about all of the medicines you take,</span> including prescription and over-the-counter medicines, vitamins and herbal supplements. LIVTENCITY may affect the way other medicines work, and other medicines may affect how LIVTENCITY works and cause serious side effects.</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">Especially tell your healthcare provider if you take a seizure (anticonvulsant) medicine.<ul class=\"Disc\">\n<li>You can ask your healthcare provider or pharmacist for a list of medicines that interact with LIVTENCITY.</li>\n<li>\n<span class=\"Bold\">Do not start a new medicine without telling your healthcare provider</span><span class=\"Bold\">.</span> Your healthcare provider will tell you if it is safe to take LIVTENCITY with other medicines.</li>\n<li>Know the medicines you take. Keep a list of your medicines and show it to your healthcare provider and pharmacist when you get a new medicine.</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">How should I take LIVTENCITY?</span>\n<ul class=\"Disc\">\n<li>Take LIVTENCITY exactly as your healthcare provider tells you to take it.</li>\n<li>Take LIVTENCITY 2 times a day.</li>\n<li>Take LIVTENCITY with or without food.</li>\n<li>Swallow LIVTENCITY tablets whole. </li>\n<li>If you are not able to swallow tablets whole, you can break apart (disperse) the tablets in drinking water <span class=\"Bold\">or</span> crush the tablets and mix with drinking water and take by mouth. <span class=\"Bold\">See the \"<a href=\"#IFU\">Instructions for Use</a>\" for detailed instructions</span> on how to prepare and give a dose of LIVTENCITY tablets by dispersing or crushing tablets and taking by mouth. </li>\n<li>If you have a Nasogastric (NG) or Orogastric (OG) Tube (French size 10 or larger), you can disperse the tablets and take through a NG or OG tube. <span class=\"Bold\">See the \"<a href=\"#IFU\">Instructions for Use</a>\" for detailed instructions</span> on how to prepare and give a dose of LIVTENCITY tablets through a NG or OG Tube. </li>\n<li>If you take too much LIVTENCITY, call your healthcare provider or go to the nearest hospital emergency room right away.</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">What are the possible side effects of LIVTENCITY?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">The most common side effects of LIVTENCITY include:</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule\"></td><td align=\"left\">\n<ul class=\"Disc\">\n<li>changes in taste</li>\n<li>nausea</li>\n<li>diarrhea</li>\n</ul>\n</td><td align=\"left\" class=\"Rrule\" colspan=\"2\">\n<ul class=\"Disc\">\n<li>vomiting</li>\n<li>tiredness</li>\n</ul>\n</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">These are not all the possible side effects of LIVTENCITY.</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">How should I store LIVTENCITY?</span>\n<ul class=\"Disc\">\n<li>Store LIVTENCITY at room temperature between 68°F to 77°F (20°C to 25°C).</li>\n</ul>\n</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">Keep LIVTENCITY and all medicines out of the reach of children.</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">General information about the safe and effective use of LIVTENCITY.</span></td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">Medicines are sometimes prescribed for purposes other than those listed in the Patient Information leaflet. Do not use LIVTENCITY for a condition for which it was not prescribed. Do not give LIVTENCITY to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about LIVTENCITY that is written for health professionals.</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">What are the ingredients in LIVTENCITY?</span></td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">Active ingredient:</span> maribavir</td>\n</tr>\n<tr>\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\"><span class=\"Bold\">Inactive ingredients:</span> FD&amp;C Blue #1, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, sodium starch glycolate, titanium dioxide, and talc.</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"left\" class=\"Lrule Rrule\" colspan=\"4\">Distributed by: <span class=\"Bold\">Takeda Pharmaceuticals America, Inc.,</span> Lexington, MA 02421<br/> LIVTENCITY<span class=\"Sup\">®</span> and the LIVTENCITY Logo<span class=\"Sup\">®</span> are registered trademarks of Takeda Pharmaceuticals International AG. TAKEDA<span class=\"Sup\">®</span> and the TAKEDA Logo<span class=\"Sup\">®</span> are registered trademarks of Takeda Pharmaceutical Company Limited. ©2024 Takeda Pharmaceuticals U.S.A., Inc. All rights reserved.<br/> For more information, go to <a href=\"http://www.explorelivtencity.com\">www.explorelivtencity.com</a> or call 1-877-TAKEDA-7 (1-877-825-3327).</td>\n</tr>\n</tbody>\n</table></div>" }

LIVTENCITY (liv-TEN-city)(maribavir)tablets, for oral use

{ "type": "p", "children": [], "text": "\nLIVTENCITY (liv-TEN-city)(maribavir)tablets, for oral use\n" }

This Instructions for Use contains information on how to prepare and give a dose of LIVTENCITY tablets by breaking apart (dispersing) or crushing in drinking water and taking by mouth; or dispersing and giving through a Nasogastric (NG) or Orogastric (OG) Tube. Read this Instructions for Use before you prepare or give the first dose of LIVTENCITY, and each time you get a refill. Ask your healthcare provider or pharmacist if you have any questions.

{ "type": "p", "children": [], "text": "This Instructions for Use contains information on how to prepare and give a dose of LIVTENCITY tablets by breaking apart (dispersing) or crushing in drinking water and taking by mouth; or dispersing and giving through a Nasogastric (NG) or Orogastric (OG) Tube. Read this Instructions for Use before you prepare or give the first dose of LIVTENCITY, and each time you get a refill. Ask your healthcare provider or pharmacist if you have any questions." }

Important information you need to know before preparing a dose of LIVTENCITY:

{ "type": "p", "children": [], "text": "\nImportant information you need to know before preparing a dose of LIVTENCITY:\n" }

{ "type": "ul", "children": [ "You can break apart (disperse) the tablets in drinking water or crush the tablets and mix with drinking water. The tablet will not be completely dispersed in the mixture.", "\nDo not mix LIVTENCITY with any liquid other than drinking water.", "LIVTENCITY tablets that have been dispersed in drinking water can be given through a Nasogastric (NG) or Orogastric (OG) tube (French size 10 or larger).", "You can prepare the mixture ahead of time and store at room temperature 68°F to 77°F (20°C to 25°C) for up to 8 hours." ], "text": "" }

Preparing a dose of LIVTENCITY by dispersing or crushing tablets and taking by mouth:

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Gather the following supplies:

{ "type": "p", "children": [], "text": "\nGather the following supplies:\n" }

{ "type": "ul", "children": [ "small, clean container to place tablets and water in", "drinking water" ], "text": "" }

Step 1: Choose a clean, flat work surface. Place all supplies on the work surface.

{ "type": "p", "children": [], "text": "\nStep 1: Choose a clean, flat work surface. Place all supplies on the work surface." }

Step 2: Wash and dry your hands well.

{ "type": "p", "children": [], "text": "\nStep 2: Wash and dry your hands well." }

Step 3: Get the prescribed number of LIVTENCITY tablets needed to prepare the dose.

{ "type": "p", "children": [], "text": "\nStep 3: Get the prescribed number of LIVTENCITY tablets needed to prepare the dose." }

Step 4: Place the LIVTENCITY tablets into the container.

{ "type": "p", "children": [], "text": "\nStep 4: Place the LIVTENCITY tablets into the container." }

Note: If you prefer, you can crush the tablets with a spoon before adding water.

{ "type": "p", "children": [], "text": "\nNote: If you prefer, you can crush the tablets with a spoon before adding water.\n" }

Step 5: Add the amount of drinking water needed for your prescribed dose.

{ "type": "p", "children": [], "text": "\nStep 5: Add the amount of drinking water needed for your prescribed dose." }

<div class="scrollingtable"><table width="50%"> <col align="center" valign="bottom" width="40%"/> <col align="center" valign="bottom" width="60%"/> <thead> <tr class="First Last"> <th align="center" class="Lrule Rrule">Number of Tablets</th><th align="center" class="Rrule">Amount of Drinking Water</th> </tr> </thead> <tbody> <tr class="Botrule First"> <td align="center" class="Lrule Rrule">2</td><td align="center" class="Rrule">30 mL</td> </tr> <tr class="Botrule"> <td align="center" class="Lrule Rrule">4</td><td align="center" class="Rrule">60 mL</td> </tr> <tr class="Last"> <td align="center" class="Lrule Rrule">6</td><td align="center" class="Rrule">90 mL</td> </tr> </tbody> </table></div>

{ "type": "table", "children": [], "text": "<div class=\"scrollingtable\"><table width=\"50%\">\n<col align=\"center\" valign=\"bottom\" width=\"40%\"/>\n<col align=\"center\" valign=\"bottom\" width=\"60%\"/>\n<thead>\n<tr class=\"First Last\">\n<th align=\"center\" class=\"Lrule Rrule\">Number of Tablets</th><th align=\"center\" class=\"Rrule\">Amount of Drinking Water</th>\n</tr>\n</thead>\n<tbody>\n<tr class=\"Botrule First\">\n<td align=\"center\" class=\"Lrule Rrule\">2</td><td align=\"center\" class=\"Rrule\">30 mL</td>\n</tr>\n<tr class=\"Botrule\">\n<td align=\"center\" class=\"Lrule Rrule\">4</td><td align=\"center\" class=\"Rrule\">60 mL</td>\n</tr>\n<tr class=\"Last\">\n<td align=\"center\" class=\"Lrule Rrule\">6</td><td align=\"center\" class=\"Rrule\">90 mL</td>\n</tr>\n</tbody>\n</table></div>" }

Step 6: Swirl the container gently to disperse the tablets in the water and swallow the mixture right away. The mixture will have a bitter taste.

{ "type": "p", "children": [], "text": "\nStep 6: Swirl the container gently to disperse the tablets in the water and swallow the mixture right away. The mixture will have a bitter taste." }

Step 7: Rinse the container with 15 mL of drinking water and swallow the mixture.

{ "type": "p", "children": [], "text": "\nStep 7: Rinse the container with 15 mL of drinking water and swallow the mixture." }

Repeat Step 7. Check that no pieces of tablet are left in the container. Repeat Step 7 until no pieces remain.

{ "type": "p", "children": [], "text": "\nRepeat Step 7. Check that no pieces of tablet are left in the container. Repeat Step 7 until no pieces remain." }

Preparing and giving a dose of LIVTENCITY through a Nasogastric (NG) or Orogastric (OG) Tube:

{ "type": "p", "children": [], "text": "\nPreparing and giving a dose of LIVTENCITY through a Nasogastric (NG) or Orogastric (OG) Tube:\n" }

Gather the following supplies:

{ "type": "p", "children": [], "text": "\nGather the following supplies:\n" }

{ "type": "ul", "children": [ "50 mL or 60 mL syringe", "drinking water" ], "text": "" }

Step 1: Remove the cap (if capped) and plunger out of a 50 mL or 60 mL syringe. Add 2 tablets into the syringe body and place the plunger back in the syringe.

{ "type": "p", "children": [], "text": "\nStep 1: Remove the cap (if capped) and plunger out of a 50 mL or 60 mL syringe. Add 2 tablets into the syringe body and place the plunger back in the syringe." }

Note: Only 2 tablets can be given through the NG or OG tube at a time.

{ "type": "p", "children": [], "text": "\nNote: Only 2 tablets can be given through the NG or OG tube at a time.\n" }

Step 2: Withdraw 30 mL of drinking water into the syringe.

{ "type": "p", "children": [], "text": "\nStep 2: Withdraw 30 mL of drinking water into the syringe." }

Step 3: Hold the syringe with the tip pointing upward. Pull the plunger back so there is some air space in the syringe. If there is a cap, place the cap back on the syringe. Shake the syringe well for about 30 to 45 seconds or until the tablets are completely dispersed. Be careful not to spill the contents of the syringe.

{ "type": "p", "children": [], "text": "\nStep 3: Hold the syringe with the tip pointing upward. Pull the plunger back so there is some air space in the syringe. If there is a cap, place the cap back on the syringe. Shake the syringe well for about 30 to 45 seconds or until the tablets are completely dispersed. Be careful not to spill the contents of the syringe." }

Step 4: Remove the cap (if capped) from the syringe again and attach the syringe to the NG or OG tube and give the mixture right away.

{ "type": "p", "children": [], "text": "\nStep 4: Remove the cap (if capped) from the syringe again and attach the syringe to the NG or OG tube and give the mixture right away." }

Step 5: Withdraw 15 mL of drinking water into the same syringe and flush through the NG or OG tube.

{ "type": "p", "children": [], "text": "\nStep 5: Withdraw 15 mL of drinking water into the same syringe and flush through the NG or OG tube." }

Repeat Step 5. Check that no pieces of tablet are left in the syringe. Repeat Step 5 until no pieces remain.

{ "type": "p", "children": [], "text": "\nRepeat Step 5. Check that no pieces of tablet are left in the syringe. Repeat Step 5 until no pieces remain." }

Note: If your prescribed dose is more than 2 tablets, Repeat Steps 1 through 5 until you give the full prescribed dose.

{ "type": "p", "children": [], "text": "\nNote: If your prescribed dose is more than 2 tablets, Repeat Steps 1 through 5 until you give the full prescribed dose." }

Storing LIVTENCITY:

{ "type": "p", "children": [], "text": "\nStoring LIVTENCITY:\n" }

{ "type": "ul", "children": [ "Store LIVTENCITY at room temperature 68°F to 77°F (20°C to 25°C)." ], "text": "" }

Keep LIVTENCITY and all medicines out of the reach of children.

{ "type": "p", "children": [], "text": "\nKeep LIVTENCITY and all medicines out of the reach of children.\n" }

For more information, go to www.explorelivtencity.com or call 1-877-TAKEDA-7 (1-877-825-3327).

{ "type": "p", "children": [], "text": "\nFor more information, go to www.explorelivtencity.com or call 1-877-TAKEDA-7 (1-877-825-3327).\n" }

Distributed by: Takeda Pharmaceuticals America, Inc., Lexington, MA 02421

{ "type": "p", "children": [], "text": "Distributed by: Takeda Pharmaceuticals America, Inc., Lexington, MA 02421" }

LIVTENCITY® and the LIVTENCITY Logo® are registered trademarks of Takeda Pharmaceuticals International AG. TAKEDA® and the TAKEDA Logo® are registered trademarks of Takeda Pharmaceutical Company Limited. ©2024 Takeda Pharmaceuticals U.S.A., Inc. All rights reserved.

{ "type": "p", "children": [], "text": "LIVTENCITY® and the LIVTENCITY Logo® are registered trademarks of Takeda Pharmaceuticals International AG. TAKEDA® and the TAKEDA Logo® are registered trademarks of Takeda Pharmaceutical Company Limited. ©2024 Takeda Pharmaceuticals U.S.A., Inc. All rights reserved." }

This Instructions for Use has been approved by the U.S. Food and Drug Administration.MAR358 R4Revised: March 2024

{ "type": "p", "children": [], "text": "This Instructions for Use has been approved by the U.S. Food and Drug Administration.MAR358 R4Revised: March 2024" }

NDC 64764-800-28

{ "type": "p", "children": [], "text": "NDC 64764-800-28" }

LIVTENCITY (maribavir) tablets 200 mg

{ "type": "p", "children": [], "text": "LIVTENCITY (maribavir) tablets 200 mg" }

Rx Only 28 Tablets

{ "type": "p", "children": [], "text": "Rx Only 28 Tablets" }

For Oral Use

{ "type": "p", "children": [], "text": "For Oral Use" }

Takeda

{ "type": "p", "children": [], "text": "Takeda" }