Amsterdam UMC
Responsive
Amsterdam, The Netherlands
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 non-small cell lung cancer (NSCLC), specifically in cases where the cancer is locally advanced and has not been treated before. The study involves several medications, including nivolumab, ipilimumab, and durvalumab. These medications are used in combination with a treatment method called chemoradiotherapy, which combines chemotherapy and radiation therapy. The purpose of the study is to compare the effectiveness of different treatment combinations in improving the time patients live without the cancer getting worse.
Participants in the study will be randomly assigned to one of three groups. One group will receive nivolumab with chemoradiotherapy followed by nivolumab and ipilimumab. Another group will receive nivolumab with chemoradiotherapy followed by more nivolumab. The third group will receive chemoradiotherapy followed by durvalumab. The study will monitor how long patients live without the cancer progressing, as well as overall survival and response to the treatment.
The trial is designed to last several years, with regular check-ups and assessments to track the progress of the disease and the effects of the treatments. The study aims to provide valuable information on the best treatment options for patients with this type of lung cancer, potentially leading to improved outcomes and quality of life for those affected by the disease.
The trial runs in 6 steps – from screening to follow-up. Each step says what happens and what the team monitors.
7 criteria
10 criteria
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Amsterdam, The Netherlands
Woluwe-Saint-Lambert, Belgium
Madrid, Spain
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is a type of medication known as an immune checkpoint inhibitor. It works by helping your immune system recognize and attack cancer cells more effectively. In this trial, it is used in combination with other treatments to help treat locally advanced non-small cell lung cancer.
is another immune checkpoint inhibitor. It helps boost the immune system's response against cancer cells. In this study, it is used alongside Nivolumab to enhance the body's ability to fight lung cancer.
is also an immune checkpoint inhibitor. It helps the immune system detect and destroy cancer cells. In this trial, it is used after chemoradiotherapy to help prevent the cancer from progressing.
Nivolumab is administered as an intravenous infusion, meaning it is given directly into the bloodstream through a vein. It is currently being studied in clinical trials for its effectiveness in treating previously untreated, locally advanced non-small cell lung cancer (LA NSCLC). The main therapeutic use of Nivolumab is to help the immune system recognize and attack cancer cells. At the molecular level, it works by blocking a protein called PD-1, which can prevent the immune system from attacking cancer cells. Nivolumab is classified as an immune checkpoint inhibitor, a type of immunotherapy.
Ipilimumab is also given as an intravenous infusion. It is being tested in combination with Nivolumab for its potential to treat LA NSCLC. The primary therapeutic indication for Ipilimumab is to enhance the immune system's ability to fight cancer. It works by blocking a protein called CTLA-4, which can inhibit the immune response against cancer cells. Ipilimumab is classified as an immune checkpoint inhibitor, similar to Nivolumab.
Durvalumab is administered through an intravenous infusion. It is being compared to other treatments in clinical trials for its role in treating LA NSCLC. The main therapeutic indication for Durvalumab is to support the immune system in targeting and destroying cancer cells. It functions by blocking the PD-L1 protein, which can help cancer cells evade the immune system. Durvalumab is also classified as an immune checkpoint inhibitor, focusing on enhancing the body's natural defenses against cancer.
sourced from the EU Clinical Trials Register and site verification
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