90
Participants
Start Date
May 1, 2023
Primary Completion Date
August 1, 2025
Study Completion Date
August 1, 2026
Letermovir Pill
Patients in the Study Group will receive virostatic prophylaxis with letermovir 480 mg qd (We will be utilizing Letermovir oral formulation of 240 mg or 480 mg as available). n all patients the virostatic prophylaxis will be initiated between days 4 and 7 after heart transplantation and the duration of virostatic prophylaxis will be determined by the Quantiferon-CMV assay.
RECRUITING
University Medical Center Ljubljana, Ljubljana
University Medical Centre Ljubljana
OTHER