Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Immune System and Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 29
- Active, not recruiting: 11
- Completed: 4
- Other: 6
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001979 — Immune System Related Kidney Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Kidney Disease; Nephrotic Syndrome |
Kidney diseases related to the immune system include, nephrotic syndrome, glomerulonephritis, membranous nephropathy, lupus nephritis, and nephritis associated with connective tissue disorders.
This study will allow researchers to admit and follow patients suffering from autoimmune diseases of the kidney. It will attempt to provide information about the causes and specific abnormalities associ…
NCT00001248 — Magnetic Resonance Imaging (MRI) to Evaluate Activity of Multiple Sclerosis (MS)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 3750 |
| Study Type | OBSERVATIONAL |
| Conditions | Multiple Sclerosis |
Studies performed under 89-N-0045 are designed to examine the natural history of multiple sclerosis (MS) using MRI and immunological measures. In addition to studying the natural history of untreated patients, the natural history of patients receiving approved disease-modifying therapies of MS will be examined. In both cohorts of patients levels of disease activity on MRI will be compared with …
NCT00001350 — Study of Autoimmune Lymphoproliferative Syndrome (ALPS)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 1200 |
| Study Type | OBSERVATIONAL |
| Conditions | Benign Lymphoproliferative Disorder |
The purpose of the protocol is to allow for patients, and relatives of patients, who may have the newly described autoimmune lymphoproliferative syndrome, to be evaluated at the NIH Clinical Center. This evaluation will include blood and relevant tissue studies along with long-term clinical evaluations to define the biology, inheritance,clinical spectrum, and natural history of this syndrome. T…
NCT00001778 — Evaluation of Patients With HAM/TSP
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 750 |
| Study Type | OBSERVATIONAL |
| Conditions | HTLV-I Infection; Tropical Spastic Paraparesis |
Objective:
Human T-lymphotropic virus type-I-associated myelopathy / tropical spastic paraparesis (HAM/TSP) is a rare neurologic disorder that affects less than 5% of patients infected with the HTLV-I virus. The purpose of this protocol is to study the natural history of HAM/TSP by monitoring clinical progression of patients longitudinally. Additionally, we will attempt to define the virologic…
NCT00006150 — Natural History, Management, and Genetics of the Hyperimmunoglobulin E Recurrent Infection Syndrome (HIES)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 600 |
| Study Type | OBSERVATIONAL |
| Conditions | Infections; Pneumonia; Immune System Diseases; STAT3 Transcription Factor; Job Syndrome |
The Hyper IgE Syndromes (HIES) are primary immunodeficiencies resulting in eczema and recurrent skin and lung infections. Autosomal dominant Hyper IgE syndrome (AD-HIIES; Job’s syndrome) is caused by STAT3 mutations, and is a multi-system disorder with skeletal, vascular, and connective tissue manifestations. Understanding how STAT3 mutations cause these diverse clinical manifestations is criti…
NCT00029445 — Leukapheresis to Obtain Plasma or Lymphocytes for Studies of HIV-infected Patients, Including Long-term Non-progressors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV |
This study will collect white blood cells and plasma for research on how the immune system controls HIV infection. The immune system of a very small group of people with HIV, called non-progressors, has been able to control HIV for long periods without antiretroviral therapy. Some immune system-related genes important for this control have been identified in these patients.
People living with …
NCT00055172 — Genetic Basis of Immunodeficiency
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Severe Combined Immunodeficiency |
This study will examine the role of hereditary factors in different forms of severe combined immunodeficiency (SCID).
Patients with immunodeficiencies may be eligible for this study. Candidates include:
- Patients with diminished numbers of T cells or NK cells or both, or
- Patients with normal T cell and NK cell numbers but diminished T cell, B cell, or NK cell function.
Relatives of patien…
NCT00128973 — Evaluation of Patients With Immune Function Abnormalities
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Granulomatous Disease (CGD); X-Linked Severe Combined Immune Deficiency (XSCID); Leukocyte Adhesion Deficiency 1 (LAD); Graft Versus Host Disease (cGvHD) |
This study will evaluate patients with abnormal immune function that results in recurrent or unusual infections or chronic inflammation. This may include inherited conditions, such as X-linked severe combined immunodeficiency (XSCID), chronic granulomatous disease (CGD), and leukocyte adhesion deficiency (LAD), or conditions resulting from outside factors, such as graft-versus-host disease (GVH…
NCT00923507 — Natural History Study of Monoclonal B Cell Lymphocytosis (MBL), Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL), Lymphoplasmacytic Lymphoma (LPL)/Waldenstrom Macroglobulinemia (WM), and Splenic Marginal Zone Lymphoma (SMZL)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Waldenstrom Macroglobulinemia; Lymphoplasmacytic Lymphoma; Monoclonal B-Cell Lymphocytosis; Small Lymphocytic Lymphoma; CLL (Chronic Lymphocytic Leukemia) |
Background
The development of new technologies now allow scientists to investigate the molecular basis and clinical manifestations of monoclonal B cell lymphocytosis (MBL), chronic lymphocytic leukemia(CLL)/small lymphocytic lymphoma (SLL), lymphoplasmacytic lymphoma (LPL)/Waldenstrom macroglobulinemia (WM), and splenic marginal zone lymphoma (SMZL). Applying these methods in a natural history…
NCT00943514 — Natural History of Bronchiectasis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 900 |
| Study Type | OBSERVATIONAL |
| Conditions | Bronchiectasis; Cystic Fibrosis; Autoimmune Disease; Common Variable Immunodeficiency |
Background:
- Bronchiectasis is a disease characterized by airways that are inflamed, abnormally dilated, and chronically infected. Individuals with bronchiectasis have a history of chronic and recurring respiratory infections. Depending on the underlying cause, these infections may involve the entire respiratory tract, resulting in sinus, ear, and lung disease.
- Bronchiectasis continues to b…
NCT01087333 — Collection of Human Samples to Study Hairy Cell and Other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1263 |
| Study Type | OBSERVATIONAL |
| Conditions | Hairy Cell Leukemia (HCL); Chronic Lymphocytic Leukemia (CLL); Non-Hodgkins Lymphoma (NHL); Cutaneous T Cell Lymphoma (CTCL); Adult T Cell Lymphoma (ATL) |
Background:
- Researchers who are studying hairy cell leukemia, and how the disease compares with other disorders, are interested in obtaining additional samples from leukemia patients and healthy volunteers. The investigators are particularly interested in samples from individuals who have diseases that can be treated with a new type of drug called immunotoxin, in which an antibody carrying …
NCT00341237 — Personalized Environment and Genes Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Environmental Health Sciences (NIEHS) |
| Enrollment | 25000 |
| Study Type | OBSERVATIONAL |
| Conditions | Diabetes; Heart Disease; Asthma |
Despite the overwhelming focus on genetic and genomic causes of human disease over the past two decades, it has been estimated that genetics is currently known to explain only 20% and 40% of the etiology of common disease. Thus, it is becoming increasingly apparent that human disease is a consequence of both genetic susceptibility and environmental exposures. Importantly, while individuals cann…
NCT01212055 — Apheresis of Patients With Immunodeficiency
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 7 |
| Study Type | OBSERVATIONAL |
| Conditions | LAD-1; DOCK8; GATA2 Deficancy |
Background:
- Gene therapy is being investigated as a possible treatment for individuals with immunodeficiency diseases or other conditions that make it difficult to fight off infection. Gene therapy avoids problems with donor identification and possible rejection of bone marrow transplant by using the patient s own modified blood cells to help treat the disease. Researchers are interested in…
NCT01422694 — Natural History and Development of Spondyloarthritis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Arthritis; Spondylitis, Ankylosing |
Background:
- Spondyloarthritis (SpA) is a group of bone and joint disorders that may cause back and joint pain and stiffness. In some cases, SpA can lead to abnormal bone growth affecting the joints and spine. Some patients have SpA without ever developing these growths, while others develop them after only a few years. Researchers are interested in studying people with SpA and their relativ…
NCT01631617 — Effects of Treatments on Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | Eczema; Dermatitis; Skin Diseases, Genetic; Dermatitis, Atopic; Skin Diseases |
| Interventions | ; ; |
Background:
- Atopic dermatitis, or eczema, is a chronic skin disorder. Patients sometimes have infections with S. aureus bacteria. Researchers want to study how eczema treatments affect the number and the type of bacteria on the skin.
Objectives:
- To study the effect of eczema treatments on skin bacteria.
Eligibility:
- Individuals between 2 and 25 years of age who have moderate to sev…
NCT01875588 — Thinking and Memory Problems in People With HIV
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 1150 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV Positive |
Background:
- People with human immunodeficiency virus (HIV) can sometimes develop thinking and memory problems. These problems can vary widely, from few symptoms to severe problems with memory and concentration. It initially was thought that good HIV treatment could prevent almost all HIV-related memory problems. However, even people with low HIV viral loads can have these problems. It may b…
NCT01861106 — Allogeneic Hematopoietic Stem Cell Transplant for GATA2 Mutations
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 144 |
| Study Type | INTERVENTIONAL |
| Conditions | GATA2; Immunodeficiency; MDS |
| Interventions | ; ; |
Background:
- GATA2 deficiency is a disease caused by mutations in the GATA2 gene. It can cause different types of leukemia and other diseases. Researchers want to see if a stem cell transplant can be used to treat this condition. A stem cell transplant will give stem cells from a matching donor (related or unrelated) to a recipient. It will allow the donor stem cells to produce healthy bone …
NCT05268289 — Study of Efficacy and Safety of LNP023 in Participants With Active Lupus Nephritis Class III-IV, +/- V
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 240 |
| Study Type | INTERVENTIONAL |
| Conditions | Lupus Nephritis |
| Interventions | ; ; |
The overall purpose of this two-part study is to evaluate the efficacy, safety and tolerability of iptacopan (LNP023) in addition to standard of care treatment.
NCT05137054 — A Study to Examine the Effects of Novel Therapy Linvoseltamab in Combination With Other Cancer Treatments for Adult Participants With Multiple Myeloma That is Resistant to Current Standard of Care Treatments
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 317 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma |
| Interventions | ; ; |
This study is researching an experimental drug called linvoseltamab in combination with other drugs for the treatment of a blood cancer called multiple myeloma. Linvoseltamab has previously been studied as a single agent (without other cancer treatments) in participants with multiple myeloma that returned after prior therapies and needed to be treated again.
In the initial study, some particip…
NCT06154252 — RESET-Myositis: An Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects With Active Idiopathic Inflammatory Myopathy or Juvenile Idiopathic Inflammatory Myopathy
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Cabaletta Bio |
| Enrollment | 74 |
| Study Type | INTERVENTIONAL |
| Conditions | Idiopathic Inflammatory Myopathy; Dermatomyositis; Anti-Synthetase Syndrome; Immune-Mediated Necrotizing Myopathy; Juvenile Dermatomyositis |
| Interventions |
RESET-Myositis: Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects with Active Idiopathic Inflammatory Myopathy or Juvenile Idiopathic Inflammatory Myopathy
NCT06133972 — Phase 3 Extension Study to Evaluate Long-term Safety of Ianalumab in Participants With Systemic Lupus Erythematosus (SIRIUS-SLE Extension).
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 550 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Lupus Erythematosus |
| Interventions | ; |
The purpose of this study is to evaluate long-term safety and tolerability of ianalumab in participants with systemic lupus erythematosus who have previously completed the treatment period in one of the two SIRIUS-SLE core studies (CVAY736F12301 or CVAY736F12302).
NCT06694558 — Monocytes in Subjects With Type 1 Diabetes and Chronic Kidney Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Cleveland Clinic |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Kidney Disease(CKD); Type 1 Diabetes (T1D) |
This is a cross-sectional study in patients with Type 1 diabetes (TID) and chronic kidney disease (CKD) to test if time in range (TIR) affects the degree of hyperglycemia required for monocyte activation, podocyte injury, and assess if monocyte activation is attenuated by glucagon-like peptide (GLP-1) agonist treatment ex vivo.
NCT06943872 — A Study to Investigate Progression-Free Survival With Sonrotoclax Plus Obinutuzumab Or Sonrotoclax Plus Rituximab Compared With Venetoclax Plus Rituximab Treatment In Patients With Relapsed and/or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CELESTIAL-RRCLL)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | BeOne Medicines |
| Enrollment | 630 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma |
| Interventions | ; ; |
The goal of this study is to compare how well sonrotoclax plus obinutuzumab works versus venetoclax plus rituximab in treating adults with relapsed and/or refractory (R/R) chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). The study will also compare how well sonrotoclax plus rituximab works versus venetoclax plus rituxumab in treating adults with R/R CLL/SLL. The safety of thes…
NCT06854159 — Odronextamab for the Treatment of Relapsed and Refractory Diffuse Large B-cell Lymphoma Before and After Chimeric Antigen Receptor T-cell Therapy
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University of California, Davis |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Diffuse Large B-Cell Lymphoma; Recurrent Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma; Refractory Diffuse Large B-Cell Lymphoma; Refractory Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma |
| Interventions | ; |
This phase II trial tests how well odronextamab works before and after standard of care (SOC) chimeric antigen receptor (CAR) T-cell therapy in treating patients with diffuse large B-cell lymphoma (DLBCL) that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). CAR-T cell therapy is the SOC treatment most patients receive when oth…
NCT07099443 — Determinants of the Response to BTK Degraders (BTKd) in Chronic Lymphocytic Leukemia
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Nantes University Hospital |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Lymphocytic Leukemia; BTK Degraders |
| Interventions |
The aim of the REBELLE cohort - bio-collection is to collect samples from patients with Chronic Lymphocytic Leukemia candidates or those exposed to BTK degraders to evaluate the mechanisms of resistance to these new molecules. To do this, an additional blood or bone marrow sample to those planned in the context of patient care or a residual lymph node biopsy sample will be collected after signi…
NCT07689331 — Hungarian National Systemic Amyloidosis Registry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Semmelweis University |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Systemic Amyloidosis; ATTR Amyloidosis; AL Amyloidosis; Amyloid Cardiomyopathy |
This registry is an observational, multicenter, retrospective and prospective, non-pharmacological study designed to collect and analyze data from patients with systemic amyloidosis treated in inpatient and outpatient cardiology, hematology, nephrology, and neurology departments across Hungary. The registry was established in 2025.
NCT07459309 — Clinical Study on the Safety, Efficacy, and Exploration of Immune Mechanisms of a Combined Multimodal Tumor Therapy System for Hepatic Malignancies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer (Primary and Metastatic); Liver Ablation |
| Interventions |
Clinical Study on the Safety, Efficacy, and Exploration of Immune Mechanisms of a Combined Multimodal Tumor Therapy System for Hepatic Malignancies
NCT07393282 — A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 270 |
| Study Type | INTERVENTIONAL |
| Conditions | High Risk Smoldering Multiple Myeloma (HR-SMM) |
| Interventions | ; |
This study is researching an experimental drug called linvoseltamab (also called “study drug”) compared to another drug called daratumumab, in participants with Smoldering Multiple Myeloma (SMM), who are at a High Risk (HR) of developing active multiple myeloma.
The aim of this study is to find out whether linvoseltamab is better than daratumumab in delaying the development of MM.
The study i…
NCT06694454 — Neoadjuvant Inhaled Azacytidine With Platinum-Based Chemotherapy and Durvalumab (MEDI4736) - a Combined Epigenetic-Immunotherapy (AZA-AEGEAN) Regimen for Operable Early-Stage Non-Small Cell Lung Cancer (NSCLC)
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-small Cell Lung Cancer (NSCLC); Carcinoma, Non-Small Cell Lung; Non-Small Cell Lung Carcinoma; Non Small Cell Lung Cancer; Non Small Cell Lung Carcinoma |
| Interventions | ; ; |
Background:
Lung cancer is the leading cause of cancer-related death worldwide. Non-small cell lung cancer (NSCLC) is the most common type of lung cancer. Surgery to remove the tumors is the standard treatment for people diagnosed with early stages of NSCLC. Despite complete removal of these tumors, many recur (happen again). An FDA-approved drug combination to treat early-stage NSCLC prior to…
Active, Not Recruiting
NCT01880567 — Ibrutinib and Rituximab in Treating Patients With Relapsed or Refractory Mantle Cell Lymphoma or Older Patients With Newly Diagnosed Mantle Cell Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 113 |
| Study Type | INTERVENTIONAL |
| Conditions | CCND1 Positive; CCND2 Positive; CCND3 Positive; CD20 Positive; Mantle Cell Lymphoma |
| Interventions | ; ; |
This phase II trial studies how well ibrutinib and rituximab work in treating patients with mantle cell lymphoma that has come back or has not responded to treatment or older patients with newly diagnosed mantle cell lymphoma. Ibrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as rituximab, may find cancer cells and …
NCT02951052 — Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Long-acting Cabotegravir Plus Long-acting Rilpivirine From Current Antiretroviral Regimen in Virologically Suppressed HIV-1-infected Adults
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | ViiV Healthcare |
| Enrollment | 618 |
| Study Type | INTERVENTIONAL |
| Conditions | Infection, Human Immunodeficiency Virus; HIV Infections |
| Interventions | ; ; |
The Antiretroviral Therapy as Long Acting Suppression (ATLAS) study is being conducted to establish if human immunodeficiency virus type-1 (HIV-1) infected adult subjects with current viral suppression on a regimen with 2 nucleoside reverse transcriptase inhibitors (NRTIs) plus a third agent, remain suppressed upon switching to a two-drug intramuscular (IM) long-acting (LA) regimen of cabotegra…
NCT03269669 — Obinutuzumab With or Without Umbralisib, Lenalidomide, or Combination Chemotherapy in Treating Patients With Relapsed or Refractory Grade I-IIIa Follicular Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 73 |
| Study Type | INTERVENTIONAL |
| Conditions | Grade 1 Follicular Lymphoma; Grade 2 Follicular Lymphoma; Grade 3a Follicular Lymphoma; Recurrent Follicular Lymphoma; Refractory Follicular Lymphoma |
| Interventions | ; ; |
This phase II trial studies how well obinutuzumab with or without umbralisib, lenalidomide, or combination chemotherapy work in treating patients with grade I-IIIa follicular lymphoma that has come back (relapsed) or does not respond to treatment (refractory). Immunotherapy with obinutuzumab, may induce changes in body’s immune system and may interfere with the ability of tumor cells to grow an…
NCT03984448 — Testing the Addition of a New Anti-cancer Drug, Venetoclax, to Usual Chemotherapy for High Grade B-cell Lymphomas
| Status | Active, not recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 363 |
| Study Type | INTERVENTIONAL |
| Conditions | Diffuse Large B-Cell Lymphoma; Diffuse Large B-Cell Lymphoma, Not Otherwise Specified; Double-Expressor Lymphoma; EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified; High Grade B-Cell Lymphoma With MYC and BCL2 or BCL6 Rearrangements |
| Interventions | ; ; |
This phase II/III trial tests whether it is possible to decrease the chance of high-grade B-cell lymphomas returning or getting worse by adding a new drug, venetoclax to the usual combination of drugs used for treatment. Venetoclax may stop the growth of cancer cells by blocking a protein called Bcl-2. Drugs used in usual chemotherapy, such as rituximab, cyclophosphamide, doxorubicin, vincristi…
NCT04212416 — Leflunomide in Treating Patients With Steroid Dependent Chronic Graft Versus Host Disease
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | City of Hope Medical Center |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Graft Versus Host Disease; Steroid Refractory Graft Versus Host Disease |
| Interventions |
This phase I trial studies the side effects of leflunomide in treating patients with steroid dependent chronic graft versus host disease (cGVHD). cGVHD is a common complication of bone marrow transplant. GVHD occurs when immune cells transplanted from a donor (the graft) recognize the transplant recipient (the host) as foreign, and cause damage to the skin, gastrointestinal tract or other organ…
NCT05070858 — A Study to Test How Safe Pozelimab and Cemdisiran Combination Therapy and Cemdisiran Alone Are and How Well They Work in Adult Patients With Generalized Myasthenia Gravis
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 288 |
| Study Type | INTERVENTIONAL |
| Conditions | Generalized Myasthenia Gravis |
| Interventions | ; ; |
This study is researching the experimental drugs called pozelimab and cemdisiran, and cemdisiran monotherapy. The study is focused on patients with generalized Myasthenia Gravis (gMG). Myasthenia gravis is a disease that causes weakness and fatigue in muscles in the body because the nerves and muscles are not communicating properly.
The aim of the study is to see how effective pozelimab and ce…
NCT05263934 — Efficacy and Safety of Depemokimab Compared With Mepolizumab in Adults With Relapsing or Refractory Eosinophilic Granulomatosis With Polyangiitis (EGPA)
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 163 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Granulomatosis With Polyangiitis |
| Interventions | ; ; |
This study aims to investigate the efficacy and safety of depemokimab compared with mepolizumab in adults with relapsing or refractory EGPA receiving SoC therapy.
NCT05409066 — Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Follicular Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Genmab |
| Enrollment | 549 |
| Study Type | INTERVENTIONAL |
| Conditions | Follicular Lymphoma (FL) |
| Interventions | ; ; |
Follicular Lymphoma (FL) is the second most common B-cell cancer and the most common type of cancer of lymphocytes. Unfortunately, this disease is incurable with conventional treatment and the disease recurs in almost all patients. This study will assess how safe and effective epcoritamab is in combination with lenalidomide and rituximab (R2) in treating adult participants with relapsed or refr…
NCT06497504 — Study of Bepirovirsen in Participants Living With Human Immunodeficiency Virus and Chronic Hepatitis B Virus Infection (B-Focus)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 153 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatitis B |
| Interventions | ; |
This study will evaluate the efficacy and safety of bepirovirsen compared to placebo in participants with human immunodeficiency virus (HIV)/hepatitis B virus (HBV) co-infection.
NCT06659627 — Interventions Against Fatigue in Patients With Myasthenia Gravis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Leiden University Medical Center |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Myasthenia Gravis; Fatigue |
| Interventions | ; ; |
A prospective assessor-blinded randomized clinical trial investigating the effect of aerobic exercise therapy or cognitive behavioural therapy on fatigue in patients with myasthenia gravis.
NCT06676033 — Epcoritamab in Chronic Lymphocytic Leukemia and Richter Syndrome
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Leukemia, Chronic Lymphocytic; Richter Syndrome |
| Interventions |
This correlative study aims to understand the pharmacodynamic effects and clonal dynamics in response to epcoritamab by obtaining and analyzing lymph node, bone marrow, and blood samples from subjects enrolled in GCT3013-03 trial sponsored by Genmab at NIH. Samples will be collected before and at multiple time points during treatment with epcoritamab. National Heart, Lung, and Blood Institute (…
Not Yet Recruiting
NCT07643974 — Coupled Gentamicin-Lactobacillus Rhamnosus in NLUTD
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | Medstar Health Research Institute |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury; Neurogenic Bladder (NB); Neurogenic Lower Urinary Tract Dysfunction; Multiple Sclerosis; Spina Bifida |
| Interventions | ; |
The main objective of the proposed research study is to determine in men and women with spinal cord injury/disease and neurogenic bladder whether the dose of coupled gentamicin & Lactobacillus rhamnosus GG affects the recolonization of the bladder, and whether the rate of success differs by sex. Secondary objectives include determining whether that recolonization lasts 7, 14, or 28 days; and s…
NCT07689604 — META 10-19 in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | Institute of Hematology & Blood Diseases Hospital, China |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Autoimmune Hemolytic Anemia (AIHA) |
| Interventions |
A Study of Metabolically Armed Autologous CD19 CAR T-Cell Therapy (META 10-19) in Patients with Relapsed/Refractory Autoimmune Hemolytic Anemia
NCT07619547 — Longitudinal Immunophenotyping of Patients With Inflammatory Bowel Disease
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Inflammatory Bowel Disease; Crohn’s Disease; Ulcerative Colitis |
Background:
Inflammatory bowel disease (IBD) is a term used to describe disorders that cause long-term inflammation in the digestive tract. Symptoms include stomach pain, diarrhea, and bleeding. Crohn’s disease and ulcerative colitis are the 2 main types of IBD. Researchers want to conduct a natural history study to learn more about whether genetic factors can cause IBD; how immune cells contr…
NCT07690683 — Patients With Hepatocellular Carcinoma (HCC)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma; Hepatocellular Cancer; Liver Diseases; Liver Cancer |
| Interventions | ; |
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide and is frequently diagnosed at an advanced stage, resulting in limited therapeutic options. Despite the advances in immunotherapy, a substantial proportion of patients fail to respond adequately due to mechanisms of immune resistance. The gut microbiota plays a crucial role in modulating the respon…
NCT07649304 — AMC 120, Glofitamab Plus Chemoimmunotherapy in Newly Diagnosed HIV-Associated Large B-Cell Lymphoma (The “Glofit-RCHOP Study”)
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | AIDS-Related Diffuse Large B-cell Lymphoma; Diffuse Large B-Cell Lymphoma, Not Otherwise Specified; High Grade B-Cell Lymphoma With MYC and BCL2 Rearrangements; High Grade B-Cell Lymphoma, Not Otherwise Specified; Lugano Classification Stage II Adult Non-Hodgkin Lymphoma AJCC v8 |
| Interventions | ; ; |
This phase I trial studies the safety and side effects of glofitamab plus a chemoimmunotherapy regimen called R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in treating patients newly-diagnosed with HIV-associated large B-cell lymphoma. Glofitamab is a bispecific monoclonal antibody, which can bind to two different antigens that are expressed by cancer cells (CD3…
Enrolling by Invitation
NCT07690761 — Rituximab+ Zanubrutinib for Patients With Hairy Cell Leukemia and Hairy Cell Variant
| Status | Enrolling by invitation |
| Phase | Phase 2 |
| Sponsor | Bnai Zion Medical Center |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Hairy Cell Leukemia; Hairy Cell Leukemia Variant |
| Interventions |
investigators propose a phase II, open label-nonrandomized, single arm, multicenter study aiming to assess the safety and efficacy with the combination of Rituximab and Zanubrutinib in patients with HAIRY CELL LUKEMIA HCL, or HAIRY CELL LEUKEMIA VARIANT-HCLv.
Completed Trials
NCT00001393 — Genetic Markers for Focal Segmental Glomerulosclerosis
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 616 |
| Study Type | OBSERVATIONAL |
| Conditions | Focal Segmental Glomerulosclerosis; HIV-Associated Focal Segmental Glomerulosclerosis |
Glomerulonephritis is a disease which affect the kidneys. Occasionally these diseases can progress to a loss of kidney function in some patients. Glomerulosclerosis or focal segmental glomerulosclerosis (FSGS) is one form of glomerulonephritis.
The cause of FSGS is unknown and often occurs on its own (idiopathic), or it can be associated with HIV (Human Immunodeficiency Virus). FSGS occurs mor…
NCT03603808 — VGX-3100 and Electroporation in Treating Patients With HIV-Positive High-Grade Anal Lesions
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | AIDS Malignancy Consortium |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Anal Intraepithelial Neoplasia; High Grade Squamous Intraepithelial Neoplasia; HIV Positivity; Human Papillomavirus-16 Positive; Human Papillomavirus-18 Positive |
| Interventions | ; ; |
This phase II trial studies the use of human papillomavirus (HPV) deoxyribonucleic acid (DNA) plasmids therapeutic vaccine VGX-3100 (VGX-3100) and electroporation in treating patients with human immunodeficiency virus (HIV)-positive high-grade anal lesions. Vaccines made from DNA may help the body build an effective immune response to kill tumor cells. Electroporation helps pores in your body’s…
NCT04196868 — Methotrexate and Metformin in Rheumatoid Arthritis Patients
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 128 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis, Rheumatoid |
| Interventions | ; ; |
Methotrexate (MTX) is the anchor drug for patients with rheumatoid arthritis (RA). Despite its marked efficacy and acceptable side effect profile, about 1/3 of patients failed to reach RA remission. Metformin is the first-line therapy for type 2 diabetes. Its antioxidative and anti-inflammatory properties make it a good candidate for the treatment of inflammatory diseases such as rheumatoid art…
NCT04868123 — Effects of TENS and Mindfulness Meditation in Persons With HIV-related Neuropathy
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers University |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; |
This study is to explore the effects of transcutaneous nerve stimulation (TENS) and mindfulness meditation in persons living with HIV (PLHIV) and painful neuropathy in the feet.