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The Hospital for Sick Children

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TORONTO, Ontario M5G 1X8

Global Leader in Brain Tumor

Global Leader in Cancer

Conducts research for Solid Tumors

Conducts research for Neuroblastoma

Conducts research for Leukemia

964 reported clinical trials

83 medical researchers

Photo of The Hospital for Sick Children in TORONTOPhoto of The Hospital for Sick Children in TORONTOPhoto of The Hospital for Sick Children in TORONTO

Summary

The Hospital for Sick Children is a medical facility located in TORONTO, Ontario. This center is recognized for care of Brain Tumor, Cancer, Solid Tumors, Neuroblastoma, Leukemia and other specialties. The Hospital for Sick Children is involved with conducting 964 clinical trials across 1,292 conditions. There are 83 research doctors associated with this hospital, such as Daniel Morgenstern, MBChir, Eric Bouffet, MD, Vijay Ramaswamy, and Glenda Courtney-Martin, PhD.

Area of expertise

1

Brain Tumor

Global Leader

The Hospital for Sick Children has run 83 trials for Brain Tumor. Some of their research focus areas include:

NTRK positive
Stage IV
MYC positive
2

Cancer

Global Leader

The Hospital for Sick Children has run 82 trials for Cancer. Some of their research focus areas include:

Stage IV
Stage III
Stage I

Top PIs

Clinical Trials running at The Hospital for Sick Children

Neuroblastoma

Testicular cancer

Crohn's Disease

Sickle Cell Disease

Cancer

Chronic Kidney Disease

Ulcerative Colitis

Inflammatory Bowel Disease

Von Willebrand Disease

Nephrotic Syndrome

Image of trial facility.

Dinutuximab + Chemotherapy

for High-Risk Neuroblastoma

This phase III trial tests how well the addition of dinutuximab to Induction chemotherapy along with standard of care surgical resection of the primary tumor, radiation, stem cell transplantation, and immunotherapy works for treating children with newly diagnosed high-risk neuroblastoma. Dinutuximab is a monoclonal antibody that binds to a molecule called GD2, which is found on the surface of neuroblastoma cells, but is not present on many healthy or normal cells in the body. When dinutuximab binds to the neuroblastoma cells, it helps signal the immune system to kill the tumor cells. This helps the cells of the immune system kill the cancer cells, this is a type of immunotherapy. When chemotherapy and immunotherapy are given together, during the same treatment cycle, it is called chemoimmunotherapy. This clinical trial randomly assigns patients to receive either standard chemotherapy and surgery or chemoimmunotherapy (chemotherapy plus dinutuximab) and surgery during Induction therapy. Chemotherapy drugs administered during Induction include, cyclophosphamide, topotecan, cisplatin, etoposide, vincristine, and doxorubicin. These drugs work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing or by stopping them from spreading. Upon completion of 5 cycles of Induction therapy, a disease evaluation is completed to determine how well the treatment worked. If the tumor responds to therapy, patients receive a tandem transplantation with stem cell rescue. If the tumor has little improvement or worsens, patients receive chemoimmunotherapy on Extended Induction. During Extended Induction, dinutuximab is given with irinotecan, temozolomide. Patients with a good response to therapy move on to Consolidation therapy, when very high doses of chemotherapy are given at two separate points to kill any remaining cancer cells. Following, transplant, radiation therapy is given to the site where the cancer originated (primary site) and to any other areas that are still active at the end of Induction. The final stage of therapy is Post-Consolidation. During Post-Consolidation, dinutuximab is given with isotretinoin, with the goal of maintaining the response achieved with the previous therapy. Adding dinutuximab to Induction chemotherapy along with standard of care surgical resection of the primary tumor, radiation, stem cell transplantation, and immunotherapy may be better at treating children with newly diagnosed high-risk neuroblastoma.

Recruiting

2 awards

Phase 3

7 criteria

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Lorlatinib + Standard Therapy

for Neuroblastoma

This phase III trial studies iobenguane I-131 or lorlatinib and standard therapy in treating younger patients with newly-diagnosed high-risk neuroblastoma or ganglioneuroblastoma. Radioactive drugs, such as iobenguane I-131, may carry radiation directly to tumor cells and not harm normal cells. Lorlatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving iobenguane I-131 or lorlatinib and standard therapy may work better compared to lorlatinib and standard therapy alone in treating younger patients with neuroblastoma or ganglioneuroblastoma.

Recruiting

2 awards

Phase 3

22 criteria

Image of trial facility.

Naxitamab

for High-Risk Neuroblastoma

Children and adults diagnosed with high-risk neuroblastoma patients with primary refractory disease or incomplete response to salvage treatment in bone and/or bone marrow will be treated for up to 101 weeks with naxitamab and granulocyte-macrophage colony stimulating factor (GM-CSF). Patients will be followed for up to five years after first dose. Naxitamab, also known as hu3F8 is a humanised monoclonal antibody targeting GD2

Recruiting

1 award

Phase 2

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