Open Label Trial of Oral Letermovir for CMV Prophylaxis in Thoracic Transplant Recipients

PHASE2RecruitingINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

April 4, 2024

Primary Completion Date

August 15, 2026

Study Completion Date

August 15, 2026

Conditions
Cytomegalovirus InfectionsTransplant-Related Disorder
Interventions
DRUG

Letermovir 480 MG [Prevymis]

"Letermovir for CMV prophylaxis in thoracic organ transplant recipients.~Letermovir will be administered by oral administration, as per study protocol. The intended duration of therapy will be up to 365 days, depending on organ transplanted and donor and recipient CMV status. However, treatment may discontinued as discussed in Section 7.~Letermovir is dosed at 480mg daily for patients with CrCl \>10. Dose adjustment, as per package insert, is recommended in setting of co-administration of cyclosporine, with dose reduction of letermovir to 240mg daily. Missed doses of letermovir will not be made up."

Trial Locations (1)

19104

RECRUITING

Penn Medicine at the University of Pennsylvania, Philadelphia

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

University of Pennsylvania

OTHER