drugset / Trial / NCT01822093

Safety Study of ADV-specific T-cells in Paediatric Patients Post Allo-HSCT

NCT01822093 ↗

NaSingle-groupOpen-labelTreatment

Summary

Human Adenovirus-specific T-cells can persist and augment impaired adenovirus immune response post allogeneic haematopoietic stem cell transplant, and reduce the requirement for antiviral therapy without toxicity or increasing the occurrence of Graft Versus Host Disease. This is a Phase I/IIa open-label safety study, assessing the effects of administering adenovirus-specific T-cells (Cytovir ADV) to paediatric patients post haematopoietic stem cell transplant.

Timeline

Start
2012-12
Primary completion
2016-12-31
Completion
2016-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Cytovir ADV Cell therapy 10000 cells/kg Other
Subject Cytovir ADV Cell therapy 100000 cells/kg Other