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NCT Number: NCT05754684

Quadruple Immunotherapy for Neuroblastoma

This is a single-arm clinical trial to evaluate the efficacy and safety of quadruple immunotherapy with natural killer (NK) cells, anti-GD2 antibody, cytokines (interleukin-2 (IL-2) and granulocyte-macrophage colony stimulating factor (GM-CSF)) and retinoid X receptor gamma (RXRg) agonist spironolactone for paediatric patients with relapsed or refractory neuroblastoma.

Recruiting

Interested in participating?

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

About this study

Included patients will receive intravenous infusion of donor NK cells on day 0, and anti-GD2 antibody (dinutuximab) on day -6 to day -2. IL-2 will be given subcutaneously on day -1, day +1, day +3, day +5, day +7, and day +9. Subcutaneous injection of GM-CSF will be started on day 0, given daily till neutrophil count >1000/mm3. Spironolactone will be started orally on day -1, given three times daily till cessation of GM-CSF.

Alternative anti-GD2 antibody (Naxitamab) can be used instead of dinutuximab, to be given on day -5, day -3, day +1 and day +3.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • relapsed or refractory neuroblastoma
  • Adequate organ function: creatinine clearance ≥40 ml/min/1.73m2, total bilirubin ≤3 times upper limit of normal and ALT ≤500 IU/L, left ventricular shortening fraction ≥25%, and oxygen saturation ≥92% in room air
  • Karnofsky or Lansky performance status score ≥50
  • Has an appropriate HLA-haploidentical NK-cell donor available

Exclusion criteria

  • Pregnant or lactating woman
  • HIV infection
  • Patients for whom conventional treatment is deemed more appropriate
  • Patients who are unlikely to benefit, e.g., terminal malignancy with life expectancy <1 month

Treatment and study plan

Natural killer cell

Biological

Natural killer cells isolated from HLA-haploidentical relative donor

Other names: NK cell

Dinutuximab Beta

Drug

Dinutuximab beta iv for 5 days

Other names: Ch14.18

Interleukin-2

Drug

Interleukin-2 sc alternate day for 6 doses

Other names: Aldesleukin

Granulocyte-macrophage colony-stimulating factor

Drug

Granulocyte-macrophage colony-stimulating factor sc daily till ANC >2,000/mm3

Other names: Sargramostim

Spironolactone

Drug

Spironolactone po three time daily

Other names: Aldactone

Naxitamab

Drug

Naxitamab iv for 4 days (as alternative for dinutuximab)

Other names: hu3F8

Primary outcomes

  1. Proportion of patients who have objective response in the tumor

    Time frame: 1-2 months

    Objective response = complete response + partial response + minor response + stable disease

Secondary outcomes

  1. Overall survival at 1 year

    Time frame: up to 1 year

    From the date of treatment start until the date of death from any cause, assessed up to 1 year

  2. Progression-free survival

    Time frame: up to 1 year

    From date of treatment start until the date of first documented progression or the date of death from any cause, whichever comes first, assessed up to 1 year

  3. Proportion of patients who have tumor relapse

    Time frame: up to 1 year

    relapse = reappearance of tumor after complete response

  4. Number of patients who experience adverse events

    Time frame: up to 1 month

    Adverse events are graded according to Cancer Therapy Evaluation Program Common Terminology Criteria for Adverse Events version 5 (CTCAEv5)

  5. Percentage of donor NK cells

    Time frame: up to 1 year

    Percentage of donor natural killer cells in the recipient's blood will be evaluated weekly from the date of NK cell infusion for 4 weeks, then every 2 weeks till donor NK cells are undetectable

Study contacts

Contact information is provided by the study sponsor or research team.

Daniel Cheuk

CONTACT

[email protected]

852-35136049

Sponsors and collaborators

Lead sponsor

Hong Kong Children's Hospital

Other

Collaborators

  • The University of Hong Kong

Registry information

Official study title

Quadruple Immunotherapy for Paediatric Patients With Relapsed or Refractory Neuroblastoma

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Mar 6, 2023
Registry last updated
Sep 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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