Region Midtjylland
Responsive
Aarhus, Denmark
Rare diseases
Investigational molecules
Locations
A plain-language summary of the goals, design and what participants do
This clinical trial is focused on studying treatments for children with certain types of brain tumors, specifically medulloblastoma, ependymoma, and atypical teratoid rhabdoid tumor (ATRT). These are serious conditions where abnormal cells form in the tissues of the brain. The study aims to explore the effectiveness of a combination of medications that target the blood vessels that supply the tumor, a process known as anti-angiogenesis therapy. The medications being tested include Cytarabine, Celecoxib, Cyclophosphamide, Etoposide, Bevacizumab, Fenofibrate, and Thalidomide. Some of these medications are given as injections, while others are taken orally as capsules.
The purpose of the study is to determine how well these treatments work in stopping the growth of these tumors. Participants in the study will receive these medications over a period of time, and their health will be monitored closely by the research team. The study will look at how the tumors respond to the treatment, whether they shrink, stay the same, or grow, and how long the patients remain free of tumor growth. The study will also monitor the overall health and quality of life of the participants during and after the treatment.
Throughout the study, participants will receive regular check-ups and tests to track their progress. The research team will evaluate the safety and side effects of the treatments, ensuring that any adverse effects are managed promptly. The study is designed to gather important information that could lead to better treatment options for children with these challenging brain tumors in the future.
The trial runs in 6 steps – from screening to follow-up. Each step says what happens and what the team monitors.
10 criteria
4 criteria
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Aarhus, Denmark
Linkoping, Sweden
Umea, Sweden
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is a treatment approach that involves giving patients lower doses of chemotherapy drugs more frequently. This method aims to minimize side effects while still effectively targeting cancer cells. In this trial, metronomic therapy is used to help control the growth of tumors by continuously attacking the cancer cells over time.
is a type of treatment that focuses on stopping the formation of new blood vessels that tumors need to grow. By cutting off the blood supply, this therapy aims to starve the tumor, preventing it from getting the nutrients it needs to expand. This approach is particularly useful in treating cancers that are known to rely heavily on blood vessel growth.
Medulloblastoma is a type of brain tumor that originates in the cerebellum, the part of the brain that controls balance and coordination. It is most commonly found in children and can spread to other parts of the brain and spinal cord. The disease progresses as the tumor grows, potentially causing symptoms such as headaches, nausea, and balance problems. As it advances, it may lead to increased intracranial pressure and neurological deficits. The tumor can also metastasize through the cerebrospinal fluid, affecting other areas of the central nervous system.
Ependymoma is a tumor that arises from ependymal cells lining the ventricles of the brain and the central canal of the spinal cord. It can occur at any age but is more common in children. The disease progresses as the tumor enlarges, potentially causing symptoms like headaches, nausea, and vision problems due to increased intracranial pressure. In the spinal cord, it may lead to back pain and neurological deficits. Ependymomas can spread within the central nervous system but rarely metastasize outside it.
Atypical Teratoid Rhabdoid Tumor (ATRT) is a rare and aggressive tumor that typically occurs in the central nervous system, often in the brain. It primarily affects young children and is characterized by rapid growth. As the disease progresses, it can cause symptoms such as headaches, vomiting, and changes in behavior or motor skills due to increased pressure on the brain. ATRT can spread to other parts of the brain and spinal cord. The tumor's aggressive nature often leads to significant neurological impairment as it advances.
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