Clinical trials located in

Nancy

Nancy city is located in France. Currently, 11 clinical trials are being conducted in this city.

Nancy, located in northeastern France, is renowned for its splendid Place Stanislas, a UNESCO World Heritage site, showcasing 18th-century architecture. This city is a hub of art and history, home to the École de Nancy, a beacon of Art Nouveau. Nancy’s influence in the art world is further highlighted by its museums, including the Musée des Beaux-Arts. The city also has a rich botanical heritage, with the Jardin botanique du Montet and Parc de la Pépinière offering lush landscapes. Nancy’s vibrant cultural scene is complemented by its historical significance in European history.

  • CT-EU-00083874

    Study to find the best way to administer pegaspargase in children with acute lymphoblastic leukemia

    This is a study to investigate treatment strategies for children and adolescents diagnosed with acute lymphoblastic leukemia (ALL). The study focuses on evaluating the efficacy of a drug called pegaspargase. The drug works by depriving tumor cells of essential nutrients, contributing to its potential efficacy against ALL in pediatric patients. The study aims to determine the optimal way to administer pegaspargase, comparing a single high dose with two lower doses, with additional doses later in treatment. For those at highest risk, a more intensive treatment plan is being investigated. This includes two larger initial doses, followed by additional doses later in treatment. The study is evaluating factors such as potential serious side effects and overall treatment efficacy.

  • Study of lacutamab in T-cell lymphoma

    This trial involves a medication called lacutamab, which will be given to patients who have a type of blood cancer known as peripheral T-cell lymphoma, and their disease has either come back after previous treatment or didn’t respond at all. Some patients in the study will receive lacutamab in combination with a common chemotherapy drugs gemcitabine and oxaliplatine, while others will get only gemcitabine and oxaliplatine. A key aim of this study is to find out if lacutamab is both safe and effective. The study is designed not to compare the two treatments directly, but to check our assumptions for deciding the number of people for the trial. The number of participants getting lacutamab is bigger.

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  • Testing relacorilant and nab-paclitaxel for various types of cancer

    The study is being conducted to investigate a new treatment for advanced ovarian, peritoneal, or fallopian tube cancer that has been unresponsive to standard treatment. The focus is on assessing whether a specific combination of drugs (Relacorilant and Nab-Paclitaxel) is more effective than using Nab-Paclitaxel alone. The primary objective is to determine if this combination can prolong the period before cancer progression without causing excessive side effects, in comparison to the use of Nab-Paclitaxel alone. Another goal is to evaluate whether the treatment can lead to a reduction in the size of the cancer and prevent further progression for an extended duration. Patients will undergo regular assessments to monitor disease progression and survival. Criteria such as RECIST, a measurement system, and a blood test checking for the presence of CA-125, a substance elevated in cancer patients, will be employed to assess disease progress.

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  • Testing Milvexian’s effectiveness in preventing repeat strokes

    This research trial, called LIBREXIA-STROKE, will test a medication called Milvexian on those who have recently had a stroke or a high-risk ‘mini-stroke’. In its 3rd testing phase, the study will involve a system where the patients won’t know whether they are receiving the actual drug or a substitute with no effect, referred to as a ‘placebo’, to maintain fairness. Milvexian is a medication that can potentially reduce the risk of having another stroke, and this trial aims to observe how effective it is in doing so. The trial will look at when the first stroke happens after starting the trial, if other major heart or limb diseases occur, or if strokes occur in the first 90 days.

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  • Comparison of different treatments for follicular lymphoma

    This study involves comparing two treatments for a condition known as follicular or marginal zone lymphoma, both of which are types of cancer affecting lymph cells. The first treatment combines zanubrutinib with an antibody called Anti-CD20, while the second treatment involves lenalidomide and rituximab. These treatments are intended for patients who have not responded or have stopped responding to conventional treatment. One of the primary objectives of the study is to determine which treatment is more effective in preventing the cancer from progressing, referred to as progression-free survival. Additionally, the study aims to assess the impact of these treatments on the patients’ quality of life, evaluating various aspects through questionnaires related to physical and emotional well-being, symptoms, and the ability to perform normal activities.

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  • Study on dazostinag & pembrolizumab for advanced solid tumors

    The purpose of this study is to test a new drug called dazostinag. A study is being conducted to see whether this drug is helpful in adults with advanced forms of solid cancer. Some people are given dazostinag alone, while others are given it with another medicine called pembrolizumab. Scientists’ focus here is on finding out whether these drugs cause any side effects, and finding out what the maximum dose is that people can take without serious side effects. The study consists of two parts, including a dose escalation phase and a dose escalation phase. In the first part, the dose of dazostinag will be gradually increased, given alone or in combination with pembrolizumab. In the second part, Dazostinag will be tested with pembrolizumab and other anticancer drugs. This section will focus on patients with specific cancers that are difficult to remove or have spread to other parts of the body.

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  • Study on Tolebrutinib’s ability to delay disability progression in multiple sclerosis

    This is a study that involves a specific type of multiple sclerosis (MS) called primary progressive multiple sclerosis (PPMS). In this study, a drug called SAR442168, also known as Tolebrutinib, will be tested against a placebo. The main purpose of the study is to see if this drug can slow down the progression of disability in PPMS. The researchers will also look at the drug’s effect on clinical markers, brain images (MRI), thinking abilities, physical function, and quality of life. They will also consider the safety and tolerability of this drug. How long each person will take the drug can vary, but it will be somewhere between 12 and 60 months.

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  • Understanding ocrelizumab treatment for progressive multiple sclerosis

    This study is exploring how well ocrelizumab works and its safety for people with progressive multiple sclerosis (MS). MS patients will either receive ocrelizumab or a placebo every 24 weeks to see if it helps with their disability, particularly in the upper limbs. The study will also monitor any side effects. It includes several phases, from initial screening to treatment and follow-ups, ending with a B-cell monitoring phase. The study, started in August 2019, is set to complete by November 2030 and includes 1000 participants who are receiving careful medical oversight.

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  • A new trial of treatment of amyotrophic lateral sclerosis with masitinib and riluzole

    This clinical trial is investigating the effects of masitinib in combination with riluzole on patients with ALS, a progressive neurodegenerative disease. The study aims to determine if masitinib can provide neuroprotection and slow the disease’s progression by modulating neuroinflammatory responses in the central and peripheral nervous systems. Participants will initially receive masitinib orally at a starting dose, which will be adjusted based on safety evaluations. The treatment’s efficacy will be monitored through clinical assessments, including ALS functional rating scales, quality of life questionnaires, and physical tests like breathing capacity and muscle strength. The trial is double-blind, meaning neither participants nor investigators know who receives masitinib or the placebo, ensuring unbiased results. The ultimate goal is to discover a treatment that can improve survival and life quality for those afflicted with ALS.

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  • Study of new drugs in acute lymphoblastic leukemia

    This clinical trial focuses on improving treatment strategies for acute lymphoblastic leukemia (ALL) in a diverse age group, from infants to young adults up to 45 years old. The study combines standard treatments with new drugs, for example, Inotuzumab Ozogamicin and Blinatumomab. The trial aims to tailor treatment to individual patient needs and reduce toxicity while maintaining treatment quality. By carefully monitoring event- and disease-free survival rates, as well as minimal residual disease responses, the trial aims to improve the standard of care for ALL and improve both survival outcomes and patient quality of life.

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  • Exploring sacituzumab govitecan for HER2-negative breast cancer care

    This study is evaluating a new treatment for patients with a certain type of breast cancer (HER2-negative) who have not had a complete response to initial chemotherapy. Participants are randomly assigned to receive the investigational drug sacituzumab govitecan or a treatment of their physician’s choice, which may be another type of chemotherapy with capecitabinalub, carboplatin or cisplatin. The study is designed to compare the effectiveness of these approaches in preventing cancer recurrence. Patients may also receive hormone therapy if needed. Patients’ safety and response to treatment are being closely monitored throughout the study.

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See more clinical trials in other cities in France:

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