Clinical Trial

Reducing Post-Letermovir CMV Infection: Efficacy of an Immune-Reconstitution-Based Scoring System to Guide Prophylaxis Duration

Not Yet Recruiting
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Summary
With the increasing use of letermovir and considering that haploidentical hematopoietic stem cell transplantation (haplo-HSCT) predominates in China alongside a high CMV seroprevalence in the population, multiple domestic centers have reported cases of CMV infection after letermovir discontinuation. Currently, there is no clear definition for the high-risk population who may benefit from extended letermovir prophylaxis. This study aims to utilize CMV-specific immune reconstitution to identify high-risk individuals for CMV infection after letermovir cessation post-transplant, thereby guiding the timing of letermovir discontinuation and balancing the risks and safety associated with prolonged prophylaxis.
Trial Details
NCT Number NCT07443501
Lead Sponsor Institute of Hematology & Blood Diseases Hospital, China
Conditions CMV Infection
Enrollment 1,114 participants
Start Date 2026-03-14
Primary Completion 2027-12-14 (estimated)
Study Completion 2027-12-14 (estimated)
Updated on ClinicalTrials.gov 2026-03-02