Clinical study of the ability of tumour lysate pulsed dendritic cells to induce anti tumour immune responses in paediatric oncology patients
DEC-NET Serial number GB514
Published online08/11/2005 16.49.00
Last updated29/11/2005 12.10.57
This trial has been approved by an ethics committee
Current trial statusOpen (actively recruiting new participants)
Major Disease
(ICD9 class)
malignant neoplasm without specification of site
Experimental drug
Autologous tumour vaccine
GenderBoth
Age (range)less than 18 years

Eligibility criteria
Inclusion criteria
Paediatric oncology patients with relapsed or resistant disease

Trial design/methodology
Phase2
Kind of studyEfficacy
Safety
DesignControlled
Purpose of study
It is hypothesised that administration of an autologous tumour vaccine, made from pulsing patients' dendritic cells with tumour protein, will be well tolerated and may result in the generation of anti-tumour immune responses. Outcome measure description: Tolerability of treatment protocol
Primary outcomes
immune anti tumour response
Secondary outcomes
tolerability and feasibility
Principal investigator
NameDr WJ Anderson
InstitutionInstitute of Child Health
Postal addressMolecular Haematology & Cancer Biology
CityLondon
CountryUNITED KINGDOM
Phone020 7242 9789 Ext 0190
Fax020 7831 0488
E-mailJ.Anderson@ich.ucl.ac.uk


Sponsor name
Great Ormond Street Hospital (NHS Trust)

ISRCTN  EudraCT