Ireland
--:--IST
Recruiting Not applicable

Engineering Immune Organoids to Study Pediatric Cancer

NCT05890781 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-05-12
Last updated
2026-02-09

Condition(s) studied

Brain TumorKidney TumorNeuroblastomaSarcoma

Investigational drug(s) / intervention(s)

Skin biopsyFresh tumor sampleBlood sample →Healthy tissue from the tumorSpinal cerebrospinal fluid (SCF)

Skin biopsy: Skin biopsy

Fresh tumor sample: Fresh tumor sample

Blood sample: Blood sample in heparin tubes (highly recommended), to be collected before starting treatment or as soon as hematological recovery has been reached

Healthy tissue from the tumor: Healthy tissue from the tumor site whenever possible

Spinal cerebrospinal fluid (SCF): Spinal cerebrospinal fluid (SCF) whenever possible

Study summary

To engineer immune organoids from pediatric patient tissues using induced-pluripotent stem cells (iPSC)

Eligibility

Sex
ALL
Min age
—
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Age at diagnosis ≤ 25 years except for patients with malignant gliomas and renal tumors for whom no upper age limit is applied * Medical suspicion or diagnosis of one of the following diseases, regardless of stage: * Brain tumors * Renal tumors * Neuroblastoma * Sarcomas * Adult patient or parents or guardians should understand, sign and date the appropriate written informed consent from prior to any protocol-specific procedures performed. Patient should be able and willing to comply with study visits and procedures as per protocol. * Affiliated to a social security system or beneficiary of the same. Exclusion Criteria: * Any histology not mentioned in the inclusion criteria * Adult patient or parents/guardians incapable/incapable of giving its/their consent * Patients deprived of their liberty by a judicial or administrative decision

Primary outcome measure(s)

  • Proportion of viable and exploitable immune organoids with engrafted tumor cells — until 5 years after enrolment

Trial sites (2)

FacilityCityRegionStatus
Gustave Roussy Villejuif France Recruiting
Hopital Necker Paris Île-de-France Region Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05890781 on ClinicalTrials.gov ↗ ← All trials in France