Recruiting PHASE1 Refractory/Relapse Neuroblastoma

New treatment option for Refractory/Relapse Neuroblastoma

Official title Clinical Trial of GAIA-102 for Refractory/Relapse Neuroblastomas and Other Malignant Pediatric Solid Tumors

ClinicalTrials.gov ID: NCT05608148

What this study is testing

What is Biological?

Biological is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for refractory/relapse neuroblastoma.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
Cohort A(GAIA-102 alone): Confirm the safety of GAIA-102 alone for refractory/relapse neuroblastoma or pediatric solid tumors with lung metastases, and decide recommended dose for Phase II. Cohort B(GAIA-102 with Dinutuximab): Confirm the safety of GAIA-102 with Dinutuximab, Filgrastim, Teceleukin combination for refractory/relapse neuroblastoma and decide recommended dose for Phase II.
  • Phase 1: an early, usually small safety study

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 1 to 24

You may be able to join if

  • Patients who have been confirmed to have the following malignant tumor by histological examination
  • cohort A : neuroblastoma or malignant solid tumor with pulmonary metastases, rhabdomyosarcoma, undifferentiated sarcoma, Ewing's sarcoma family...
  • cohort B : neuroblastoma.
  • cohort C \& D : neuroblastoma and other malignant solid tumors, rhabdomyosarcoma, Ewing's sarcoma family, hepatoblastoma.
  • Undergoing the following treatment.

You likely can't join if

  • Patients with brain metastases.
  • Patients diagnosed with cancerous meningitis
  • Patients who received allogeneic hematopoietic stem cell transplant.
  • Patients with active autoimmune disease.
See the full eligibility criteria
Who can join
  • Patients who have been confirmed to have the following malignant tumor by histological examination
  • cohort A : neuroblastoma or malignant solid tumor with pulmonary metastases, rhabdomyosarcoma, undifferentiated sarcoma, Ewing's sarcoma family, osteosarcoma, other cartilage sarcoma, nephroblastoma, hepatoblastoma...
  • cohort B : neuroblastoma.
  • cohort C \& D : neuroblastoma and other malignant solid tumors, rhabdomyosarcoma, Ewing's sarcoma family, hepatoblastoma.
  • Undergoing the following treatment.
  • cohort A \& B : Patients who have the resistance for more than two treatment regimens, and the resistance for all standard regimens based on the guideline.
  • cohort C \& D : Patients with neuroblastoma who have completed the dinutuximab regimen and still have residual tumor. Patients with rhabdomyosarcoma, Ewing's sarcoma family, hepatoblastoma who have the resistance for...
  • Patients who have medical history for serious side effect , allergy reaction with regards to concomitant drugs.
  • Patients aged from 1years to 24 years at the time of obtaining consent.
  • Patients with performance status(PS) over 50 (Lansky Performance Status Score less than 16 years old) or (Karnofsky Performance Status over 16 years old) at the time of obtaining consent.
What rules you out
  • Patients with brain metastases.
  • Patients diagnosed with cancerous meningitis
  • Patients who received allogeneic hematopoietic stem cell transplant.
  • Patients with active autoimmune disease.

The study team makes the final eligibility decision.

Where it's taking place

  • Fukuoka, Fukuoka, Japan

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 1 year to 24 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Fukuoka, Fukuoka, Japan. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.