Letermovir for Secondary Prophylaxis in Solid Organ Transplant Recipients

Eligibility Criteria

• 1. Adult (\> 18 years old) solid organ transplant recipients (heart, kidney or liver patients) recovering from treated CMV disease in whom the clinician deems that the patient need secondary prophylaxis and in whom written informed consent is obtained.
• 2. Patient able to participate with follow up for 6 months
• 3. Not enrolled in competing clinical trials
• 1. Patients with creatinine clearance less than 10 ml per min at time of enrollment
• 2. Hypersensitivity to letermovir or has a CMV isolate which is known to be resistant to letermovir based on prior testing
• 3. On CVVH or renal dialysis at the time of enrollment
• 4. Has Child Pugh Class C severe hepatic insufficiency at screening.
• 5. Has both moderate hepatic insufficiency AND moderate to severe renal insufficiency at screening.
• 6. Has a history of malignancy ≤5 years prior to signing informed consent except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer or carcinoma in situ; or is under evaluation for other active or suspected malignancy.
• 7. Is pregnant or expecting to conceive, is breastfeeding, or plans to breastfeed from the time of consent through at least 90 days following cessation of study therapy.
• 8. Is expecting to donate eggs or sperm starting from the time of consent through at least 90 days following cessation of study therapy.
• 9. Has a history or current evidence of any condition, therapy, lab abnormality, or other circumstance that might confound the results of the study, interfere with the participant's participation for the full duration of the study, or put the participant at undue risk, as judged by the investigator, such that it is not in the best interest of the participant to participate in this study.
• 10. Is, at the time of signing informed consent, a user of recreational or illicit drugs or has had a recent history (within the 6 months) of drug or alcohol abuse or dependence.
• 11. Is currently participating or has participated in a study with an unapproved investigational compound or device within 28 days, or 5× half-life of the investigational compound (excluding monoclonal antibodies), whichever is longer, of initial dosing on this study. Participants previously treated with an investigational monoclonal antibody will be eligible to participate after a 150-day washout period.
• 12. Has previously participated or is currently participating in any study involving administration of a CMV vaccine or another CMV investigational agent that is not approved or is planning to participate in a study of a CMV vaccine or another unapproved CMV investigational agent during the course of this study.