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Molecular and Immunological Characterisation of High Risk CHildhood Cancer At DiagnOsis, Treatment and Follow-up - Biological Evaluation in Children, Adolescents and Young Adults -
Methodology: Prospective, multicentric, open, non-randomised, non-therapeutic, interventional study
To identify and characterise: * meaningful molecular genetic alterations, * meaningful immunological features of high risk childhood, adolescents and young adult cancers, at diagnosis, during patient treatment and follow-up (time dimension).
Age
1 - 25 years
Sex
ALL
Healthy Volunteers
No
Chu D'Amiens Picardie
Amiens, France
CHU Angers
Angers, France
CHRU de Besançon - Hôpital Jean-Minjoz
Besançon, France
CHU de Bordeaux - Hôpital des enfants - Groupe Hospitalier Pellegrin
Bordeaux, France
CHRU de Brest
Brest, France
CHU CAEN
Caen, France
Centre Régional de Cancérologie et Thrapie Cellulaire Pdiatrique (CRCTCP)
Clermont-Ferrand, France
CHU Hôpital d'Enfants
Dijon, France
CHU GRENOBLE Alpes - Hôpital Couple-Enfant
Grenoble, France
Centre Oscar Lambret
Lille, France
Start Date
April 20, 2018
Primary Completion Date
April 19, 2027
Completion Date
August 19, 2027
Last Updated
March 18, 2025
600
ESTIMATED participants
Sampling on blood, bone marrow and cerebrospinal fluid
OTHER
Lead Sponsor
Institut Curie
NCT04936529
NCT06541262
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04851119