Efficacy of Extended Letermovir Prophylaxis to Prevent CMV Reactivation in High-Risk Chinese Adults Undergoing Allogeneic HSCT

NARecruitingINTERVENTIONAL
Enrollment

330

Participants

Timeline

Start Date

December 16, 2024

Primary Completion Date

December 1, 2025

Study Completion Date

December 31, 2025

Conditions
Cytomegalovirus InfectionsCMV
Interventions
DRUG

Letermovir (0-24w)

Patients will begin receiving prophylactic treatment with domestically produced letermovir from day 0 to day 28 post-allo-HSCT, at a dose of 480 mg, administered orally once daily. If used in combination with cyclosporine, the dose should be reduced to 240 mg once daily. The treatment will continue until 24 weeks post-transplant (approximately 170 days).

DRUG

Letermovir (0-14w)

Patients will begin receiving prophylactic treatment with domestically produced letermovir from day 0 to day 28 post-allo-HSCT, at a dose of 480 mg, administered orally once daily. If used in combination with cyclosporine, the dose should be reduced to 240 mg once daily. The treatment will continue until 14 weeks post-transplant (approximately 100 days).

Trial Locations (1)

215006

RECRUITING

Hematology Department, The First Affiliated Hospital of Soochow University, Suzhou

All Listed Sponsors
lead

The First Affiliated Hospital of Soochow University

OTHER