drugset / Trial / NCT01822093
Safety Study of ADV-specific T-cells in Paediatric Patients Post Allo-HSCT
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cytovir ADV | Cell therapy | 10000 cells/kg | Other |
| Subject | Cytovir ADV | Cell therapy | 100000 cells/kg | Other |