Alternate Donor Study of Pre-Emptive Cellular Therapy

PHASE2CompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

October 31, 2010

Primary Completion Date

December 31, 2013

Study Completion Date

January 31, 2014

Conditions
Cytomegalovirus Infection
Interventions
BIOLOGICAL

CMV-specific T-cells, single infusion following single positive CMV PCR result

"1. Intravenous ganciclovir 5mg/kg twice daily~2. Oral valganciclovir 900mg twice daily~3. Intravenous foscarnet 90 mg/kg twice daily"

Trial Locations (9)

Unknown

QEH Birmingham Hospital, Birmingham

Bristol Royal Hospital, Bristol

Kings College Hospital, London

Royal Free Hospital, London

Manchester Royal Infirmary, Manchester

The Christie, Manchester

Nottingham University Hospital - City Campus, Nottingham

Churchill Hospital, Oxford

WC1E 6BT

University College London Hospital, London

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Leukaemia Lymphoma Research

OTHER

collaborator

National Health Service, Blood and Transplant

UNKNOWN

collaborator

University of Birmingham

OTHER

lead

Cell Medica Ltd

INDUSTRY

NCT01220895 - Alternate Donor Study of Pre-Emptive Cellular Therapy | Biotech Hunter | Biotech Hunter