drugset / Trial / NCT05708755

CMV Immunity Monitoring in Lung Transplant Recipients

NCT05708755

Phase 2 Recruiting 50 enrolled NYU Langone Health Viracor Eurofins · collab
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to determine the safety and feasibility of using a laboratory test to guide duration of antiviral prophylaxis with valganciclovir (medication used to prevent viral infections) after lung transplant. The laboratory test, inSIGHT™ CMV T Cell Immunity Panel, measures patients' immune response to a common viral infection known as cytomegalovirus (CMV). The goal of this study will be to safely decrease how long patients need to take valganciclovir based on the results of the CMV T Cell Immunity Panel.

Timeline

Start
2024-09-13
Primary completion
2027-05
Completion
2028-05

Drugs

EvaluationDrugModalityDoseRoute
Background Valganciclovir Small molecule 900 mg

Indications

No indication recorded.