Trials / Recruiting
RecruitingNCT06555432
A Study of LIVTENCITY (Maribavir) in Adults With Cytomegalovirus (CMV) Infection After Transplantation in South Korea
Post-Marketing Surveillance (Usage Results Study) of LIVTENCITY Tablet (Maribavir) for the Approved Indications in South Korea
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 168 (estimated)
- Sponsor
- Takeda · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
Cytomegalovirus (CMV) is a common virus that infects many people. It can cause serious illness in people with weak immune systems especially in those undergoing transplants. LIVTENCITY (Maribavir) is a medicine approved for treating CMV infection in adults after transplant in South Korea. The main aim of this study is to learn how safe and effective LIVTENCITY (Maribavir) is in treating adults with CMV infection after transplant in a routine clinical practice setting. During the study, a participant's data will be collected for about 5 months (20 weeks). The study does not have fixed visits to the hospital, but it is recommended to visit the study doctor approximately 6 times during study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | LIVTENCITY | LIVTENCITY tablet. |
Timeline
- Start date
- 2024-11-14
- Primary completion
- 2028-10-01
- Completion
- 2028-10-01
- First posted
- 2024-08-15
- Last updated
- 2025-11-18
Locations
1 site across 1 country: South Korea
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06555432. Inclusion in this directory is not an endorsement.