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ReclutamentoFASE2, FASE3INTERVENTISTICO

A Safety and Efficacy Study of hu14 in High-Risk Neuroblastoma Patients

This research study is looking into a new treatment for high-risk neuroblastoma, a type of cancer mainly found in young children. The treatment involves a new medicine called hu14.18K322A (also known as daretabart), which is a type of antibody, given alongside standard chemotherapy drugs (Temozolomide and Irinotecan). The main goal is to find out how safe and effective this combination treatment is for children and young people aged 18 months to 18 years whose neuroblastoma has come back or not responded well to previous treatments. It will also help determine the best dose of the new medicine to use.

A colpo d'occhio

Stato
Reclutamento
Fase
FASE2, FASE3
Sponsor
Renaissance Pharma Ltd.
Obiettivo di iscrizione
144
Inizio
30 Mar 2026
Completamento stimato
01 Mar 2031

Di cosa tratta questo studio?

Neuroblastoma is a type of cancer that usually affects children under five years old. It starts in nerve cells outside the brain, often in the tummy or chest. For many children, this cancer is considered 'high-risk' because it has spread to other parts of the body. When the cancer spreads, it can be harder to treat, and sadly, it can come back even after initial treatment.

This study is looking at a new medicine called hu14.18K322A, also known as daretabart, which is a specially designed antibody. Antibodies are natural substances in your body that fight off illness. This new medicine is designed to target and attack cancer cells. In this study, it will be given alongside two chemotherapy medicines, Temozolomide and Irinotecan, which are drugs already used to treat cancer by stopping cancer cells from growing and dividing.

The main aim of this study is to learn more about how well this combination of medicines works and whether it is safe for children and young people with high-risk neuroblastoma. The hope is that this new combination could offer a better way to treat the cancer, especially for those whose cancer has returned or hasn't responded to other treatments. The study will first check for the best dose of hu14.18K322A to use, and then test its effects on a larger group of patients.

Punti chiave

  • This study is for children and young people with high-risk neuroblastoma that has come back or not responded to past treatments.
  • It tests a new antibody medicine (hu14.18K322A) combined with chemotherapy.
  • The main goals are to find a safe dose and see how well the combination works.
  • Participants will receive up to 12 cycles of treatment and be closely monitored.
  • There are strict health checks to make sure it's safe for your child to join.
  • You can stop taking part in the study at any time.

Chi può essere idoneo?

To join this study, children and young people must be between 18 months and 18 years old when their parents or guardians give permission. They must have a confirmed diagnosis of high-risk neuroblastoma that has spread to other parts of the body. Doctors will also need to be able to measure or see the cancer clearly to check how well the treatment is working.

Participants should also generally be well enough to take part. This means they should have recovered from any serious side effects of past chemotherapy treatments. There are also specific checks to make sure important organs like the heart, kidneys, liver, and lungs are working well enough, and that their blood counts are at safe levels.

It's important that any previous major surgery for the cancer was at least two weeks ago. If a patient has had cancer in their brain or spinal cord before, it must be completely gone and showing no signs of activity. For young women who can have children, a negative pregnancy test is needed, and both males and females need to agree to use effective contraception during and for a period after the study.

Questo studio potrebbe fare al caso tuo?

Rispondi a queste domande rapide per vedere se potresti essere idoneo. Questo è solo una guida — il team di ricerca prende la decisione finale.

  1. Is your child between 18 months and 18 years old?
  2. Has your child been diagnosed with high-risk neuroblastoma that has spread?
  3. Has your child recovered from previous cancer treatments?
  4. Are your child's important organs (heart, kidneys, liver, lungs) generally working well?
  5. Is your child able to move around and do daily activities fairly well?
  6. If female and able to have children, is she using birth control and has had a negative pregnancy test?
Rispondi a ogni domanda per vedere il tuo risultato.

Cosa comporta la partecipazione?

If you decide to take part in this study, your child will receive up to 12 cycles of treatment. A 'cycle' is a period of treatment followed by a break. The specific details of how often the medicine is given will be explained by the study team. Throughout the treatment, your child will have regular check-ups, blood tests, and scans to monitor their health, see how well the treatment is working, and check for any side effects.

Initially, a small group of 12 patients will help doctors find the best dose of the new medicine. Once this dose is confirmed, up to 132 more patients will join the study. Each treatment cycle will involve visits to the hospital. After the treatment finishes, your child will continue to be monitored for a longer period to understand any long-term effects of the treatment. The total duration of follow-up will be discussed with you by the study team.

Rischi e benefici potenziali

Taking part in a clinical trial might offer the chance to receive a new treatment that isn't widely available yet, which could potentially help your child. However, there's no guarantee that the treatment will work for everyone, and it might not be better than existing treatments. Like all medicines, the new treatment and chemotherapy drugs can have side effects, which could be mild or more serious. The study team will carefully monitor your child for these effects and will explain all known risks to you before you decide to take part. Remember, you have the right to withdraw your child from the study at any time, for any reason, without it affecting their ongoing medical care.

Locations (19)

  • University of California San Francisco (UCSF)
    Codice postale verificato
    San Francisco, Stati Uniti· Reclutamento
  • Children's Hospital Colorado Anschutz Medical
    Codice postale verificato
    Aurora, Stati Uniti· Reclutamento
  • The University of Chicago
    Codice postale verificato
    Chicago, Stati Uniti· Reclutamento
  • University of Minnesota Masonic Children's Hospital
    Codice postale verificato
    Minneapolis, Stati Uniti· Reclutamento
  • The Children's Hospital at Montefiore
    Codice postale verificato
    Il Bronx, Stati Uniti· Reclutamento
  • Duke University Medical Center
    Codice postale verificato
    Durham, Stati Uniti· Reclutamento
  • Children's Hospital of Philadelphia
    Codice postale verificato
    Philadelphia, Stati Uniti· Reclutamento
  • University of Texas Southwestern
    Codice postale verificato
    Dallas, Stati Uniti· Reclutamento
  • L'Ospedale per Bambini Malati
    Codice postale verificato
    Toronto, Canada· Reclutamento
  • Rigshospitalet
    Codice postale verificato
    Copenaghen, Danimarca· Reclutamento
  • Institut Curie
    Codice postale verificato
    Parigi, Francia· Reclutamento
  • Gustave Roussy
    Codice postale verificato
    Villejuif, Francia· Reclutamento

Domande comuni

What is high-risk neuroblastoma?

It's a type of cancer found in young children, usually under five, where the cancer has spread from where it started to other parts of the body, making it harder to treat.

What is hu14.18K322A (daretabart)?

It's a new antibody-based medicine designed to specifically target and attack neuroblastoma cancer cells. It's being tested with chemotherapy in this study.

Will my child definitely get the new treatment?

Yes, all participants in this study will receive the combination of hu14.18K322A and chemotherapy, as it's testing a specific combination of medicines.

How long will the study last for my child?

Your child could receive up to 12 cycles of treatment, and then there will be a period of follow-up monitoring to check their health over the long term. The exact duration will be explained.

Can we stop participating at any time?

Yes, you can withdraw your child from the study at any point, for any reason, and this will not affect their regular medical care.

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