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Engineering Immune Organoids to Study Pediatric Cancer

Engineering Immune Organoids to Study Pediatric Cancer (IMMUNE-ORGANOIDS)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05890781
Acronym
IMMUNEORGANOID
Enrollment
108
Registered
2023-06-06
Start date
2023-05-12
Completion date
2028-05-01
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Tumor, Kidney Tumor, Neuroblastoma, Sarcoma

Brief summary

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

Interventions

PROCEDURESkin biopsy

Skin biopsy

PROCEDUREFresh tumor sample

Fresh tumor sample

BIOLOGICALBlood sample

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

PROCEDUREHealthy tissue from the tumor

Healthy tissue from the tumor site whenever possible

PROCEDURESpinal cerebrospinal fluid (SCF)

Spinal cerebrospinal fluid (SCF) whenever possible

Sponsors

Gustave Roussy, Cancer Campus, Grand Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 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

Design outcomes

Primary

MeasureTime frame
Proportion of viable and exploitable immune organoids with engrafted tumor cellsuntil 5 years after enrolment

Countries

France

Contacts

CONTACTClaudia PASQUALINI, MD
claudia.pasqualini@gustaveroussy.fr+33 (0)1 42 11 55 31
CONTACTJérémy MIONE, MS
jeremy.mione@gustaveroussy.fr+33 (0)1 42 11 42 11

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026