Clinical trials located in

Amiens

Amiens city is located in France. Currently, 20 clinical trials are being conducted in this city.

Amiens, nestled in northern France, is renowned for its Gothic Amiens Cathedral, a UNESCO World Heritage Site and one of the largest classic Gothic churches of the 13th century. The city is also famous for the floating gardens known as “Hortillonnages,” spanning over 300 hectares of marshland, interlaced with canals navigated by traditional flat-bottomed boats. Amiens was the birthplace of French President Emmanuel Macron and the backdrop for several novels by Jules Verne, who lived there for 18 years. The city played a pivotal role during both World Wars, showcasing its resilience and historical significance.

  • CT-EU-00117859

    Isatuximab Plus Pomalidomide and Dexamethasone for AL Amyloidosis

    This clinical trial is focused on patients with AL Amyloidosis who have not achieved a very good partial response or better following previous therapies. The trial investigates the efficacy of combining Isatuximab, Pomalidomide, and Dexamethasone. The aim is to see if this drug combination can significantly reduce the levels of misfolded proteins in the blood, which are characteristic of this disease, thereby improving the condition and potentially prolonging life. This study seeks to offer a new potential treatment option for those who have limited responses to existing therapies.

    • Isatuximab
  • Study of the drug combination mRNA-4157/V940 and Pembrolizumab in the treatment of melanoma

    The aim of this clinical trial is to test whether a new drug called mRNA-4157/V940 in combination with pembrolizumab can help prevent the recurrence of melanoma in people who have already had it. Currently, mRNA-4157/V940 is what is called “individualized neoantigen therapy,” which means it is a therapy created specifically for each patient based on their cancer cells. Doctors give this drug along with pembrolizumab, a drug that helps the immune system fight cancer cells.

    The main goal of this study is to determine whether taking V940 and pembrolizumab together is more effective in preventing melanoma recurrence than taking pembrolizumab alone. Researchers will closely monitor how long it takes for the cancer to return or spread. The study will last for approximately 74 months.

    • mRNA-4157/V940
    • placebo
    • Pembrolizumab
  • Combining Azacitidine and Venetoclax for Higher-Risk Chronic Myelomonocytic Leukemia

    The AVENHIR study is an open-label clinical trial for patients with higher-risk chronic myelomonocytic leukemia, a type of blood cancer. This study will evaluate the effectiveness and safety of combining two drugs: Azacitidine and Venetoclax (also known as ABT-199). Azacitidine is a chemotherapy drug, while Venetoclax is a targeted therapy that works by blocking a specific protein in cancer cells.

    The main goals of the study are to determine the overall response rate to this drug combination, which means how many patients achieve complete remission, partial remission, or clinical benefit. The study will also closely monitor safety and any potential dose-limiting side effects during the first two treatment cycles.

    To be eligible for this study, patients must be newly diagnosed with higher-risk chronic myelomonocytic leukemia and have not received any prior treatment with hypomethylating agents like Azacitidine.

    • Venetoclax
  • Study on Ravulizumab’s effect on Immunoglobulin A Nephropathy

    The study is looking into the effectiveness of a medication called ravulizumab for adults who have a kidney condition known as Immunoglobulin A Nephropathy (IgAN). This condition can lead to kidney damage over time, and the study aims to find out if ravulizumab can help reduce the amount of protein lost in urine—a common problem in IgAN—and slow down the decrease in kidney function.

    In this study, about 450 participants who are at a high risk of their disease getting worse will be chosen. These participants must have been on stable treatment for their IgAN for at least three months before the study starts. They will then receive either ravulizumab or a placebo, which is a treatment with no active drug, through an IV infusion based on their weight. The main goal is to see if those who receive ravulizumab have a significant improvement in their condition compared to those who receive the placebo.

    The study will have two main checkpoints. The first one, at Week 34, will check how much protein is in the urine, and the second one, at Week 106, will assess how well the kidneys are filtering waste from the blood. Additionally, a smaller group of participants with more advanced kidney issues will receive ravulizumab to further explore its effects.

    After the study ends at Week 106, participants will have the option to continue receiving ravulizumab in a follow-up period to see how long-term treatment affects their condition. This study is a chance for people with IgAN to potentially slow down their disease progression and improve their quality of life.

    • placebo
    • Ravulizumab
  • 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.

    • pegaspargase
  • Venetoclax in recurrence of blood cancer after previous stem cell transplantation

    This study aims to investigate the effectiveness and safety of a novel treatment approach, combining the drugs venetoclax and azacitidine, along with donor lymphocyte infusion (DLI) in patients experiencing a relapse of one of two of blood-related disorders: myelodysplastic syndrome (condition where blood cells do not develop properly) or acute myeloid leukemia (bone marrow cells become abnormal and begin to accumulate in excess), following stem cell transplantation. The study involves a group of patients for whom standard treatments have not yielded satisfactory results. The objective is to understand whether the combination of new drugs and donor lymphocyte infusion can effectively control these blood disorders, especially after stem cell transplantation. Researchers are monitoring side effects, assessing disease progression, and determining the safety of the procedure. The results may provide valuable insights into effective therapeutic strategies for these challenging blood-related disorders.
    • azacitidine
    • venetoclax
  • Improving psoriasis treatment for patients: a study on brodalumab

    This detailed study focuses on individuals with moderate-to-severe plaque psoriasis who weigh more than 120 kg. It aims to find out if adjusting the dose of the medication brodalumab can lead to better skin health. In this study, participants receive either an adjusted higher dose of brodalumab or the standard dose. Researchers closely monitor the skin’s response to the treatment, checking if the adjusted dose leads to better skin clearance, meaning fewer or no psoriasis symptoms.

    • Brodalumab
  • Testing the effectiveness of a new drug compared with standard therapy in the treatment of asthma

    This medical research is a year-long study that tests a new asthma medication, called GSK3511294 (Depemokimab), against two other asthma medicines, Mepolizumab and Benralizumab. The trial is intended for teens and adults who have a severe form of asthma called ‘eosinophilic phenotype.’ The aim is to see if switching to GSK3511294 from Mepolizumab or Benralizumab keeps the severity and frequency of asthma attacks under control equally or better. Participants will keep taking their regular non-biological asthma medications throughout the trial. The study will look at the number of severe asthma attacks a patient experiences in a year, which is defined here as any worsening of asthma requiring steroids, a hospital visit, or an emergency room trip. They will also check for changes in their quality of life and their asthma control using questionnaires, and measure the capacity of their lungs with a breathing test.

    • GSK3511294 (Depemokimab)
    • Mepolizumab
    • Benralizumab
  • 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.

    • Lacutamab
    • Oxaliplatine
    • Gemcitabine
  • Evaluating effects of pembrolizumab with chemotherapy and radiation for esophageal cancer

    This trial explores the impact of a drug called pembrolizumab on patients with a specific kind of cancer, Esophageal Carcinoma. It compares two treatments. Some patients will receive the standard treatment (chemotherapy and radiation), plus a placebo. Others will receive the standard treatment (chemotherapy and radiation) plus Pembrolizumab. The reason for doing it is to see if Pembrolizumab, when added to normal treatment, can help patients live without their cancer getting worse, or live longer overall. During the trial, patients will either be given pembrolizumab or placebo, as well as one of two chemotherapy combinations and radiation treatment, for about a year.

    • Pembrolizumab
    • levoleucovorin
    • leucovorin
    • 5-Fluorouracil
    • Cisplatin
    • Oxaliplatin
  • Testing the safety and effectiveness of alpelisib for MCAP syndrome

    This study is testing a medication called Alpelisib in people with a rare condition called Megalencephaly-Capillary Malformation Polymicrogyria Syndrome (MCAP). The study will be split into two sections. The first is a 6-month trial where some people will be given Alpelisib and others a placebo (a harmless, inactive substance), but no one will know which group they are in. This is to precisely measure the medication’s effects. After this, all qualifying participants will receive Alpelisib for the remaining 18 months. Participants’ progress will be monitored regularly, and the effects of the medicine will be assessed primarily using a scale that measures improvement in everyday skills and quality of life. The study also examines the medicine’s impact on brain growth and function using MRI scans and other tests.

    • Alpelisib
  • Studying ustekinumab treatment for Crohn’s perianal fistula

    This is a medical study being conducted to examine how effective a certain medication, called Ustekinumab, can be for people suffering from Crohn’s disease, specifically a subset called perianal Crohn’s. A group of people suffering from moderate to severe forms of this disease will be randomly assigned to receive either the actual medication or a placebo. Their symptoms will then be tracked for a period of 48 weeks to see if the medication helps lessen their symptoms. The end goal is to see whether the drug is useful in stopping all abnormal openings (fistulas) from draining. The study also aims to ensure that the drug doesn’t cause any buildup of more than 2 cm.

    • Ustekinumab
  • Study on using a new drug combination to treat solid tumors

    This is a study that focuses on the use of a drug known as E7386, which is combined with other anticancer drugs, in patients who have solid tumors. The main goal of the trial is to see how safe and tolerable this combination of drugs is, and to figure out the best dosage for the second phase of this study. The study will assess how patients react to the drug, track any side effects they might experience, and measure how well the drug is working in their bodies. Researchers will check if the drug can get rid of the cancer (complete response) or at least shrink it (partial response), keep the cancer the same size (stable disease), or if the cancer continues to grow (progressive disease). The study will also measure how long it takes for the cancer to worsen or for the patient to pass away (overall survival).

    • E7386- new potential medication for solid tumors
    • Lenvatinib
  • Different treatment combinations for advanced pancreatic cancer study

    This trial is about trying out different ways to control late-stage pancreatic cancer. The current standard treatment for patients with this type of cancer is a mix of drugs called FOLFIRINOX (Leucovorin (Folinic Acid), Fluorouracil, Irinotecan). However, doctors are not sure when they should stop or reduce this treatment after the cancer has been controlled for a while. So, in this study, they want to see if a new drug called OSE2101 can help keep the cancer from getting worse. Patients will either get OSE2101 with FOLFIRI (a kind of maintenance therapy), or FOLFIRI alone after the FOLFIRINOX treatment is stopped. The study also aims to assess the safety of OSE2101 in patients with advanced pancreatic cancer.

    • Tedopi/OSE2101
    • Irinotecan
    • Leucovorin
    • Fluorouracil
  • 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.

    • Zanubrutinib
    • Obinutuzumab
    • Lenalidomide
    • Rituximab
  • 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.

    • Dazostinag
    • Platinum
    • Pembrolizumab
    • 5-Fluorouracil
  • Examining combination treatment for Myelofibrosis

    This study is about testing a new combination of drugs known as KRT-232 (Navtemadlin) and TL-895 in patients with a blood disorder called Myelofibrosis. Doctors want to see how well this combination can work for patients who have tried other treatments without success, or those who can’t tolerate another medicine called JAK inhibitor. The first two groups will go through a process of adjusting doses to find the most tolerable and effective amount of medicine. The third group will be a larger set of patients, and this part of the trial will only continue if the treatment shows enough promise in the early stages. One of the ways to measure success is through a noticeable reduction in spleen size, measured by scans at 24 weeks. Doctors will also assess the patients’ symptoms using a special form.

    • Navtemadlin/KRT-232
    • TL-895- new potential medication for hematologic malignancies
  • Examining new treatment for digestive complications of Graft Versus Host Disease

    This study is examining the effects of a therapy called MaaT013 in patients who do not respond well to a drug called Ruxolitinib. Patients suffer from a disease called acute GVHD that affects their stomach. Previous studies have shown promising results, with most patients showing improvement after receiving MaaT013. Due to these results, MaaT013 will be used as “rescue therapy” in patients who do not improve with steroids or JAK inhibitors, drugs often used to treat the disease. The standard first treatment for acute GVHD is steroids, but some patients do not respond well to this treatment, and those who do may have serious side effects if they take high doses for a long time. Therefore, scientists are interested in exploring alternative treatments such as MaaT013. A drug called Ruxolitinib was approved by the FDA in 2019, but again, not all patients respond well to this treatment, prompting the need to develop alternatives.

    • MaaT013- new potential medication for gastrointestinal acute graft-versus-host disease
  • Comparing abelacimab and apixaban treatments for blood clots in cancer patients

    This research study is looking at how two different medicines, abelacimab and apixaban, can help people with a severe medical problem called Cancer Associated Thrombosis (CAT). CAT happens when blood clots form inside the veins (a condition called Venous Thromboembolism or VTE) in people with cancer. These blood clots can cause other serious health issues. In this study, the researchers will see if abelacimab (which is given monthly) is as good as apixaban if not better (which you take twice a day every day) for six months. And then look at whether the blood clots come back, if any bleeding happens, and if patients had to stop treatment.

    • Abelacimab
    • Apixaban
  • Testing astegolimab’s effectiveness in chronic obstructive pulmonary disease patients

    A clinical research study is being conducted to examine the efficacy and safety of a novel treatment known as astegolimab in the management of Chronic Obstructive Pulmonary Disease (COPD). The study is particularly focused on individuals with a history of COPD who are either current or former smokers and have experienced frequent exacerbations. Within the scope of this study, astegolimab’s therapeutic potential is being compared to that of a placebo. Participants enrolled in the trial will be administered the study medication at intervals of either every 2 or 4 weeks. Key parameters under evaluation include the frequency of COPD exacerbations, variations in the quality of life of the participants, and changes in lung function over the course of the study. The study aims to contribute valuable data to medical research, particularly in understanding the treatment dynamics of astegolimab in COPD management.

    • Astegolimab

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