Houston, TXNCT03294954Now EnrollingIRB Ready

Neuroblastoma Clinical Trial in Houston, TX

Access cutting-edge neuroblastoma treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by Baylor College of Medicine

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Expert Care in Houston

Access neuroblastoma specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related neuroblastoma treatment provided free

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Check if you qualify for this neuroblastoma clinical trial in Houston, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Houston site if eligible
  4. 4Begin participation

About This Neuroblastoma Study in Houston

This research study combines two different ways of fighting cancer: antibodies and Natural Killer T cells (NKT). Antibodies are types of proteins that protect the body from infectious diseases and possibly cancer. T cells, also called T lymphocytes, are special white blood cells that can kill other cells, including cells infected with viruses and tumor cells. Both antibodies and T cells have been used to treat patients with cancers. Investigators have found from previous research that they can put a new gene into T cells that will make them recognize cancer cells and kill them. In a previous clinical trial, investigators made artificial genes called a chimeric antigen receptors (CAR), from an antibody called 14g2a that recognizes GD2, a molecule found on almost all neuroblastoma cells (GD2-CAR). Investigators put these genes into the patients' own T cells and gave them back to patients that had neuroblastoma. NKT cells are another special subgroup of white blood cells that can specifically go into tumor tissue of neuroblastoma. Inside the tumor, there are other white blood cells called macrophages which help the cancer cells to grow and recover from injury. NKT cells can specifically kill these macrophages and slow the tumor growth. We will expand NKT cells and add GD2-specific chimeric antigen receptors to the cells. We think these cells might be better able to attack NB since they also work by destroying the macrophages that allows the tumor to grow. The chimeric antigen receptor will also contain a gene segment to make the NKT cells last longer. This gene segment is called CD28. In addition, to further improve the antitumor activity of the GINAKIT cells we added another gene expressing a molecule called Interleukin -15 (IL-15). The combination of these 3 components showed the most antitumor activity by CAR expressing NKT cells and improved these cells' survival in animal models. We also found that a medicine called ETANercept can slow down neuroblastoma growth, which might enhance the effects of the modified cells. In this part of our study, we aim to treat children with hard-to-treat neuroblastoma using these modified NKT cells along with ETANercept. Though ETANercept has been used to treat other diseases, such as rheumatoid arthritis in children, there is limited information about the safety, efficacy, and risk of ETANercept treatment in combination with cellular therapies. GD2-CAR expressing NKTs have not been tested in patients so far. The purpose of this study is to find the largest effective and safe dose of GD2-CAR NKT cells (GINAKIT cells), to evaluate their effect on the tumor and how long they can be detected in the patient's blood and what affect they have on the patient's neuroblastoma.

Sponsor: Baylor College of Medicine

Who Can Participate

Inclusion Criteria

Relapsed or refractory high risk neuroblastoma
Life expectancy of at least 12 weeks
Age greater than 1 year and less than 21 years old
Karnofsky/Lansky score of 60% or greater
Absence of HAMA prior to enrollment (only in patients that have been previously treated with murine antibodies)
Ability to tolerate leukocyte apheresis
Informed consent and assent (as applicable) obtained from parent/guardian and child.
Patients must have an ANC greater than or equal to 500/µl, platelet count greater than or equal to 20,000/µl. Patients may be transfused to obtain a platelet count greater than or equal to 20,000/µl.
Pulse Ox greater than or equal to 90% on room air
Serum AST less than 3 times the upper limit of normal
Total Bilirubin less than 1.5 times the upper limit of normal
Creatinine \< 1.5 times the upper limit of normal
Recovered from the acute toxic effects of all prior chemotherapy based on the enrolling physician's assessment (if some effects of chemotherapy are expected to last long term, patient is eligible if meeting other eligibility criteria).
Weight greater than 12kg
Negative QuantiFERON-TB or T-SPOT testing within 3 months prior to procurement Procurement

Exclusion Criteria

Rapidly progressive disease
History or hypersensitivity to murine protein-containing products
Tumor causing airway obstruction
Currently receiving immunosuppressive drugs such as corticosteroids, tacrolimus or cyclosporine
Severe previous toxicity from cyclophosphamide or fludarabine based on the enrolling physician's assessment
HIV infection
History of hypersensitivity, anaphylaxis, and/or adverse event with Etanercept Treatment Inclusion Criteria:
Relapsed or refractory high risk neuroblastoma
Life expectancy of at least 12 weeks
Age greater than 1 year and less than 21 years old
Karnofsky/Lansky score of 60% or greater
Patients must have an ANC greater than or equal to 500/µl, platelet count greater than or equal to 20,000/µl. Patients may be transfused to obtain a platelet count greater than or equal to 20,000/µl.
Pulse Ox greater than or equal to 90% on room air
Serum AST less than 3 times the upper limit of normal
Total Bilirubin less than 1.5 times the upper limit of normal
Creatinine \< 1.5 times the upper limit of normal
Recovered from the acute toxic effects of all prior chemotherapy based on the enrolling physician's assessment (if some effects of chemotherapy are expected to last long term, patient is eligible if meeting other eligibility criteria and expected to tolerate lymphodepletion).
Absence of human anti-mouse antibodies (HAMA) prior to enrollment for patients who have received prior therapy with murine antibodies
Patients must have autologous transduced NKTs with greater than or equal to 20% expression of GD2-specific CAR.
Informed consent and assent (as applicable) obtained from parent/guardian and child.
Weight greater than 12kg
Negative QuantiFERON-TB or T-SPOT testing within 3 months prior to the start of LD Treatment Exclusion Criteria:
Rapidly progressive disease
Currently receiving any investigational drugs
History or hypersensitivity to murine protein-containing products
Cardiomegaly or bilateral pulmonary infiltrates on chest radiograph or CT. However, patients with cardiomegaly on imaging may be enrolled if they have an assessment of cardiac function (i.e., ECHO or MUGA) within 3 weeks of starting protocol therapy that is within normal limits. Additionally, patients with bilateral pulmonary infiltrates on imaging may be enrolled if the lesions are not consistent with active neuroblastoma (i.e., negative on functional imaging with PET or MIBG, or by pathologic assessment).
Tumor potentially causing airway obstruction
Pregnancy or lactation or not willing to use birth control
Currently receiving immunosuppressive drugs such as corticosteroids, tacrolimus or cyclosporine
Severe previous toxicity form cyclophosphamide or fludarabine based on the enrolling physician's assessment
HIV infection
History of hypersensitivity, anaphylaxis, and/or adverse event with Etanercept

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Houston?

Yes, this clinical trial (NCT03294954) has an active research site in Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Neuroblastoma Treatment Options in Houston, TX

If you're searching for neuroblastoma treatment options in Houston, TX, this clinical trial (NCT03294954) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced neuroblastoma specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all neuroblastoma clinical trials near you to find additional studies recruiting in your area.

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