CMV-TCIP Directed Letermovir Prophylaxis After Allo-SCT

PHASE2RecruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

June 27, 2024

Primary Completion Date

June 30, 2028

Study Completion Date

June 30, 2029

Conditions
CMVAllogeneic Stem Cell Transplantation
Interventions
DRUG

Letermovir

Subjects will receive 14 weeks of letermovir prophylaxis at standard recommended dose follow by CMV-TCIP-directed extended prophylaxis.

DEVICE

CMV T Cell Immunity Panel (CMV-TCIP)

Viracor CMV-TCIP assay to measure how a person's immune system responds to CMV. Viracor CMV-TCIP will be measured monthly, starting at week 14, until positive, then at week 30 and 52.

DIAGNOSTIC_TEST

CMV DNA PCR

Plasma level of CMV DNA PCR will be measured at enrollment and at least weekly through week 30, then at least every 2 weeks through week 52 of transplant if no GVHD or CMV reactivation.

Trial Locations (1)

92868

RECRUITING

Chao Family Comprehensive Cancer Center, University of California Irvine, Orange

All Listed Sponsors
collaborator

Eurofins Viracor

UNKNOWN

lead

University of California, Irvine

OTHER