drugset / Trial / NCT05914701

Secondary Prophylaxis of CMV Infection Using Letermovir After HID-HSCT

NCT05914701

NaSingle-groupOpen-labelTreatment

Summary

To evaluate the efficacy and safety of secondary prophylaxis of CMV reactivation, clinically significant CMV infection with oral letermovir in Chinese haplo-HSCT patients, as well as treatment-related mortality, all-cause mortality and QoL after transplantation. For enrolled patients, Letermovir would be administered at a dose of 480 mg per day (or 240 mg per day in patients taking cyclosporine). The regimen duration of dosing was approximately 120 days or 16 weeks. Or physicians could adjust regimen duration according to the CMV infection risk factors.

Timeline

Start
2023-07-01
Primary completion
2024-12-31
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Letermovir Small molecule 240 mg
Subject Letermovir Small molecule 480 mg

Indications

No indication recorded.