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Anti-GD2 CAR T Cells in Pediatric Patients Affected by High Risk and/or Relapsed/Refractory Neuroblastoma or Other GD2-positive Solid Tumors

28 septembre 2026 mis à jour par: Franco Locatelli, Bambino Gesù Hospital and Research Institute

Phase I/II Study of Anti-GD2 Chimeric Antigen Receptor-Expressing T Cells in Pediatric Patients Affected by High Risk and/or Relapsed/Refractory Neuroblastoma or Other GD2-positive Solid Tumors

The purpose of this study is to test the safety and efficacy of GD2-CART01, a CAR T cell treatment targeting GD2 in paediatric or young adult patients with High Risk and/or relapsed/refractory Neuroblastoma.

A small exploratory cohort of patients with GD2-positive tumors other than Neuroblastoma has also been included.

Aperçu de l'étude

Description détaillée

The study will consist of 2 phases, a Phase I or dose escalation phase and a Phase II or expansion phase. Paediatric or young adult patients with relapsed High Risk and/or relapsed/refractory Neuroblastoma will be enrolled in the study.

After completion of the phase I portion of the study, a small cohort of patients with GD2-positive tumors other than Neuroblastoma has also been included.

Eligible patients will undergo leukapheresis in order to harvest T cells, which will be manufactured to obtain the autologous CAR T product GD2-CART01, a GD2-targeting CAR T product. Briefly, the patients will be treated with a lymphodepleting regimen containing conventional chemotherapic agents and subsequently will receive a single infusion of GD2-CART01. Moreover, the product contains a suicide gene safety switch (namely inducible Caspase 9): in case of relevant toxicities, the patient will receive the dimerizing agent in order to activate the apoptotic pathway in the infused T cells.

After infusion of CAR T cells, the patients will enter a 5-year active follow-up period.

Type d'étude

Interventionnel

Inscription (Estimé)

42

Phase

  • Phase 2
  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Roma, Italie
        • Ospedale Pediatrico Bambino Gesù

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

1 an à 25 ans (Enfant, Adulte)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

Phase I The patient must meet the following eligibility inclusion criteria to be enrolled to receive treatment in the Phase I study.

  1. Diagnosis of NBL that have been treated with frontline therapy and is judged to be incurable, based upon the following criteria:

    1. Relapse after first-line treatment, proved by a positive 123-I-mMIBG-scan
    2. Persistence/progression of disease after the initiation of the upfront treatment
  2. Patients must have measurable or evaluable disease at the time of treatment enrollment, as shown by bone marrow biopsy/aspirate, US or CT/MRI scan or by 123-I-mMIBG scan.

  3. Recover from the toxic effect of previous chemotherapies: grade 4 and or 3 non-hematologic toxicities must have resolved to grade ≤2; if some effects of the therapies have become chronic (i.e. treatment associated thrombocytopenia), the patient must be clinically stable, according to the opinion of the treating physicians, and meet all other eligibility criteria.

  4. Age: 12 months -18 years.

  5. Voluntary informed consent is given. For subjects < 18 years old their legal guardian must give informed consent. Pediatric subjects will be included in age appropriate discussion and verbal assent will be obtained for those greater than or equal to 12 years of age, when appropriate.

  6. Clinical performance status: Patients > 16 years of age: Karnofsky greater than or equal to 60%; Patients less than or equal to 16 years of age: Lansky scale greater than or equal to 60%.

  7. Patients of child-bearing or child-fathering potential must be willing to practice birth control from the time of enrollment on this study and for four months after receiving the preparative regimen.

  8. Females of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects on the fetus.

Phase II

The patient must meet the following eligibility inclusion criteria to be enrolled to receive treatment in the Phase II study.

  1. Diagnosis of NBL that have been treated with frontline therapy and is judged to be incurable, based upon the following criteria:

    1. Relapse after first-line treatment, proved by a positive MIBG-scan
    2. Persistence/progression of disease after the initiation of the upfront treatment

    OR

  2. Diagnosis of extremely High Risk NBL at high risk of relapse, defined by stage III/IV and Myc-N amplification, at the end of the first-line treatment according to the Standard of Care, even if NED.

    OR

  3. Diagnosis of GD2+ tumors other than Neuroblastoma, considered incurable with conventional treatments by the treating physician.

  4. Patients with relapsed/refractory disease must have measurable or evaluable disease at the time of treatment enrollment, as shown by bone marrow biopsy/aspirate, US or CT/MRI scan or by MIBG-scan.

  5. Recover from the toxic effect of previous chemotherapies: grade 4 and or 3 non-hematologic toxicities must have resolved to grade ≤2; if some effects of the therapies have become chronic (i.e. treatment associated thrombocytopenia), the patient must be clinically stable, according to the opinion of the treating physicians, and meet all other eligibility criteria.

  6. Age: 12 months - 18 years.

  7. Voluntary informed consent is given. For subjects < 18 years old their legal guardian must give informed consent. Pediatric subjects will be included in age appropriate discussion and verbal assent will be obtained for those greater than or equal to 12 years of age, when appropriate.

  8. Clinical performance status: Patients > 16 years of age: Karnofsky greater than or equal to 60%; Patients less than or equal to 16 years of age: Lansky scale greater than or equal to 60%.

  9. Patients of child-bearing or child-fathering potential must be willing to practice birth control from the time of enrollment on this study and for four months after receiving the preparative regimen.

  10. Females of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects on the fetus

Exclusion Criteria:

  1. Pregnant or lactating women

  2. Severe, uncontrolled active intercurrent infections

  3. Active hepatitis B or hepatitis C infection

  4. HIV infection

  5. Rapidly progressive disease with life-expectancy < 6 weeks

  6. History of grade 3 or 4 hypersensitivity to murine protein-containing products

  7. Hepatic function: Inadequate liver function defined as total bilirubin > 4x upper limit of normal (ULN) or transaminase (ALT and AST) > 6 x ULN based on age and laboratory specific normal ranges

  8. Renal function: serum creatinine > 3x ULN for age.

  9. Blood oxygen saturation < 90%.

  10. Cardiac function: Left ventricular ejection fraction lower than 45% by ECHO.

  11. Marrow function: ANC lower than 500/mm3 and/or platelets lower than 20.000 (not reached by transfusion).

  12. Congestive heart failure, cardiac arrhythmia, psychiatric illness, or social situations that would limit compliance with study requirements or in the opinion of the PI would pose an unacceptable risk to the subject.

  13. Untreated CNS metastasis; patients with previous CNS tumor involvement that has been treated and is stable for at least 6 weeks following completion of therapy are eligible.

  14. Concurrent or recent prior therapies, before infusion:

    1. Systemic steroids (at a dose equivalent to or greater 2 mg/kg prednisone) in the 2 weeks before infusion. Recent or current use of inhaled/topical/non-absorbable steroids is not exclusionary.
    2. Systemic chemotherapy in the 2 weeks preceding infusion.
    3. Immunosuppressive agents less than or equal to 30 days.
    4. Radiation therapy must have been completed at least 3 weeks prior to enrollment.
    5. I131-MIBG therapy must have been completes at least 6 weeks prior to enrollment
    6. Anti-GD2 murine monoclonal antibody (ch14.18 antibody) in the 2 weeks preceding infusion
    7. Other anti-neoplastic investigational agents currently or within 30 days prior to start of protocol therapy;
    8. Exceptions:
    9. Subjects receiving steroid therapy at physiologic replacement doses only are allowed provided there has been no increase in dose for at least 2 weeks prior to starting apheresis
  15. Patient-derived GD2-CART01 production failure.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: GD2-CART01

After a lymphodepleting regimen the patients will receive 1.0 to 10.0 x 10⁶/kg GD2 Chimeric Antigen Receptor (CAR) positive T cells.

Following a lymphodepleting treatment with conventional chemotherapy, patients will be treated with 1.0 to 10.0 x 10⁶/kg GD2 Chimeric Antigen Receptor (CAR) positive T cells as a single dose.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Phase I - Identification of the dose limiting toxicity (DLT)
Délai: 4 weeks after T cell infusion

Toxicity will be assessed according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) scale, version 4 and the number of patients experiencing DLT will be evaluated

4 weeks after T cell infusion
Phase II - Antitumor effect
Délai: Up to 6 months after T cell infusion

Assessment of Best Overall Response (BOR)

Up to 6 months after T cell infusion

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Temps de progression (TTP)
Délai: Jusqu'à 5 ans après la perfusion de lymphocytes T
Jusqu'à 5 ans après la perfusion de lymphocytes T
Survie sans événement (EFS)
Délai: Jusqu'à 5 ans après la perfusion de lymphocytes T
Jusqu'à 5 ans après la perfusion de lymphocytes T
Survie globale (SG)
Délai: Jusqu'à 5 ans après la perfusion de lymphocytes T
Jusqu'à 5 ans après la perfusion de lymphocytes T
In vivo persistence/expansion of infused CAR T cell
Délai: UP to 5 years

Detection of infused CAR T cell in the peripheral and bone marrow blood

UP to 5 years
Serum cytokine profiling
Délai: First 2 weeks after T cell infusion

Assessment of the seric cytokines profile

First 2 weeks after T cell infusion
Disease outcome according to INRC vs irRC
Délai: Up to 5 years

Tumor response assessment through the two different criteria

Up to 5 years
Elimination of CAR T cell through iC9 in case of toxicity
Délai: Up to 15 years

Assessment of the kinetic of CAR T cell elimination after infusion of the dimerizer

Up to 15 years

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

5 janvier 2018

Achèvement primaire (Estimé)

1 décembre 2026

Achèvement de l'étude (Estimé)

1 décembre 2027

Dates d'inscription aux études

Première soumission

6 décembre 2017

Première soumission répondant aux critères de contrôle qualité

8 décembre 2017

Première publication (Réel)

14 décembre 2017

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

28 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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