Non-Hodgkin Lymphoma Clinical Trials
64 studies are recruiting for non-hodgkin lymphoma in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Venetoclax, Ibrutinib, Prednisone, Obinutuzumab, and Revlimid (ViPOR) in Relapsed/Refractory B-cell Lymphoma
Background: B-cell lymphoma is a cancer of white blood cells found in the lymph nodes. It affects the system that fights infections and disease. Researchers want to learn how certain drugs work together to treat B-cell lymphomas. The drugs are venetoclax, ibrutinib, prednisone, obinutuzumab, and le…
- Stage
- Phase 1
- Ages
- 18 to 120
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Cancer Institute (NCI)
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Safety and Preliminary Efficacy of MT-601 in Patients With Relapsed/Refractory Lymphoma
This study is a Phase 1 multicenter study with a Dose Escalation and Dose Expansion evaluating safety and efficacy of MT-601 administration to patients with Relapsed or Refractory Lymphoma. The starting dose administered is 200 x 10\^6 cells (flat dosing).
- Stage
- Phase 1
- Ages
- 18 to 100
- Site
- City of Hope, Duarte, California
- Locations
- 7 in total
- Run by
- Marker Therapeutics, Inc.
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AZD3470 as Monotherapy or in Combination With Anticancer Agent(s) in Participants With Haematologic Malignancies.
This study is designed to evaluate the safety, tolerability, PK, pharmacodynamics, and preliminary efficacy following oral administration of AZD3470 as a monotherapy, and in combination with other anticancer agents in participants with haematologic malignancies.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Research Site, Duarte, California
- Locations
- 39 in total
- Run by
- AstraZeneca
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A Dose-Escalation and Expansion Study of Tacabrutideg (BGB-16673) in Participants With B-Cell Malignancies
Study consists of two main parts to explore tacabrutideg recommended dosing, a Phase 1 monotherapy dose finding comprised of monotherapy dose escalation and monotherapy safety expansion of selected doses, and a Phase 2 (expansion cohorts)
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Alabama At Birmingham Hospital, Birmingham, Alabama
- Locations
- 115 in total
- Run by
- BeOne Medicines
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Rituximab (Rtx) + Tafasitamab in Combination With Allogeneic NK Cells for Treatment of Relapsed/Refractory (r/r) B-cell Non-Hodgkin Lymphoma (NHL)
This research study is for people who have relapsed or refractory B-cell non-Hodgkin's lymphoma (NHL) that has not responded to two or more lines of therapy. The purpose of this study is to identify the recommended dose of allogeneic NK cells in combination with IL-2, Tafasitamab and Rituximab for …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Case Comprehensive Cancer Center, Cleveland Clinic Foundation Taussig Cancer Institute, Cleveland, Ohio
- Locations
- 2 in total
- Run by
- Paolo Caimi, MD
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Dose-escalation and Dose-expansion Study of Safety of Azer-cel (PBCAR0191) in Participants With Relapsed/Refractory (r/r) Non-Hodgkin Lymphoma (NHL) and r/r B-cell Acute Lymphoblastic Leukemia (B-ALL)
This is a Phase 1/1b, nonrandomized, open-label, parallel assignment, dose-escalation, and dose-expansion study to evaluate the safety and clinical activity of azer-cel, an allogeneic anti-CD19 CAR T, in adults with r/r B ALL, r/r B-cell NHL and CLL/SLL.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- H. Lee Moffitt Cancer Center, Tampa, Florida
- Locations
- 15 in total
- Run by
- Imugene Limited
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Toxin Exposure and Immune Dysregulation in Non-Hodgkin Lymphoma
The goal of this observational cohort study is to learn how toxin and occupational exposures, germline genetic variation, and immune dysregulation relate to B-cell non-Hodgkin lymphoma among active-duty service members and other Military Health System beneficiaries. The main questions are whether s…
- Stage
- Not phased
- Ages
- 4 and older
- Site
- Walter Reed National Military Medical Center, Bethesda, Maryland
- Locations
- 3 in total
- Run by
- Henry M. Jackson Foundation for the Advancement of Military Medicine
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Pomalidomide and Dose-Adjusted EPOCH +/- Rituximab for HIV-Associated Lymphomas
Background: Non-Hodgkin lymphoma (NHL) is the most common cancer among people living with HIV in the United States. People with HIV are up to 17 times more likely to get NHL than people who do not have HIV. The disease may also be different in these two groups. More study is needed for treating peo…
- Stage
- Phase 1
- Ages
- 18 to 120
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Cancer Institute (NCI)
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Study of Rondecabtagene Autoleucel in Aggressive Large B-Cell Lymphoma
This is a Phase 1/2, multi-center, open-label study evaluating the safety and efficacy of rondecabtagene autoleucel (ronde-cel) also known as LYL314, a dual-targeting chimeric antigen receptor (CAR) targeting cluster of differentiation (CD)19 and CD20 in participants with aggressive large B-cell ly…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California-Irvine Medical Center, Irvine, California
- Locations
- 35 in total
- Run by
- Lyell Immunopharma, Inc.
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LV20.19 CAR T-Cells in Combination With Pirtobrutinib for Relapsed, Refractory B-cell Malignancies
This is a phase I, interventional, single arm, open label, treatment study designed to evaluate the safety and efficacy of LV20.19 CAR -T cells with pirtobrutinib bridging and maintenance in adult patients with B cell malignancies that have failed prior therapies.
- Stage
- Phase 1
- Ages
- 18 to 81
- Site
- Froedtert & the Medical College of Wisconsin, Milwaukee, Wisconsin
- Run by
- Medical College of Wisconsin
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Gene Therapy for CD19-Positive Hematologic Malignancies (SENTRY-CD19)
This is a Phase 1/2, first-in-human, open-label, dose-escalating trial designed to assess the safety and efficacy of VNX-101 in patients with relapsed or refractory CD19-positive hematologic malignancies.
- Stage
- Phase 1
- Ages
- 13 to 90
- Site
- City of Hope, Duarte, California
- Locations
- 11 in total
- Run by
- Vironexis Biotherapeutics Inc.
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A Study of Voice as a Way to Monitor for Side Effects in People Receiving CAR T-Cell Therapy
The purpose of this study is to collect voice recordings and nervous system (neurologic) assessments from people with non-Hodgkin lymphoma (NHL) or multiple myeloma (MM) who are receiving standard treatment with CAR T-cell therapy. Researchers will study whether these voice recordings and assessmen…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey
- Locations
- 8 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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Sample Collection for Ongoing Research and Product Evaluation Study - Non-Hodgkin Lymphoma (SCORE-NHL)
The SCORE-NHL study is a prospective, multi-center, study designed to collect data and biological samples from participants diagnosed with aggressive Stage I to IV non-Hodgkin Lymphoma (NHL). Study participants will undergo research blood collections of up to 60 mL as well as residual tissue collec…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Natera, Inc., Austin, Texas
- Run by
- Natera, Inc.
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Lentiviral Gene Therapy (Zamtocabtagene Autoleucel) LTFU
This is an observational long-term follow-up (LTFU) study for subjects who previously received zamtocabtagene autoleucel, known as MB-CART2019.1.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Banner MD Anderson Cancer Center, Gilbert, Arizona
- Locations
- 11 in total
- Run by
- Miltenyi Biomedicine GmbH
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A Study to Investigate Ronde-cel Versus Investigator's Choice CD19 CAR T-Cell Therapy
This Phase 3 study compares rondecabtagene autoleucel (ronde-cel), a dual-targeting CD19/CD20 CAR T-cell therapy, with investigator's choice of CD19 CAR T-cell therapy in patients with relapsed or refractory large B-cell lymphoma in the second-line setting.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Banner MD Anderson Cancer Center, Gilbert, Arizona
- Locations
- 36 in total
- Run by
- Lyell Immunopharma, Inc.
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A Study to Evaluate Efficacy, Safety, and PK of XEMBIFY®+Standard Medical Treatment (SMT) Compared to Placebo+SMT to Prevent Infections in Participants With HGG and Recurrent or Severe Infections Associated With B-cell Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma
The primary purpose of the study is to evaluate whether biweekly administered XEMBIFY® plus Standard Medical Treatment (SMT) over a one-year period will reduce the rate of major bacterial infections per participant per year in B-cell CLL, MM, and NHL participants with hypogammaglobulinemia (HGG) in…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- GC2202 Study Site 115, Huntington Park, California
- Locations
- 62 in total
- Run by
- Grifols Therapeutics LLC
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A Vaccine (CMV-MVA Triplex Vaccine) for the Enhancement of CMV-Specific Immunity and the Prevention of CMV Viremia in Patients Undergoing Haploidentical Hematopoietic Stem Cell Transplant
This phase Ib trial tests the safety, side effects, and how well cytomegalovirus (CMV)-modified vaccinia Ankara (MVA) Triplex vaccine works in enhancing CMV-specific immunity and preventing CMV viremia in patients undergoing haploidentical hematopoietic stem cell transplant. Haploidentical stem cel…
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- City of Hope Medical Center, Duarte, California
- Locations
- 3 in total
- Run by
- City of Hope Medical Center
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Cord Blood Transplant, Cyclophosphamide, Fludarabine, and Total-Body Irradiation in Treating Patients With High-Risk Hematologic Diseases
This phase II trial studies how well giving an umbilical cord blood transplant together with cyclophosphamide, fludarabine, and total-body irradiation (TBI) works in treating patients with hematologic diseases. Giving chemotherapy, such as cyclophosphamide, fludarabine and thiotepa, and TBI before …
- Stage
- Phase 2
- Ages
- 0 to 65
- Site
- Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington
- Run by
- Fred Hutchinson Cancer Center
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Constitutive IL7R (C7R) Modified Banked Allogeneic CD30.CAR EBVSTS for CD30-Positive Lymphomas
This study involves patients with diffuse large B cell lymphoma (DLBCL), natural killer/T-cell lymphoma (NKTL), or classical Hodgkin lymphoma (cHL) (referred to collectively as lymphoma) whose disease has returned or not responded to treatment. Previous research combined antibodies and T cells to t…
- Stage
- Phase 1
- Ages
- 12 to 75
- Site
- Houston Methodist Hospital, Houston, Texas
- Locations
- 2 in total
- Run by
- Baylor College of Medicine
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Repurposing Riluzole for Cancer-Related Cognitive Impairment: A Pilot Trial
This is a phase 2a, randomized, double-blinded, placebo-controlled pilot clinical trial determining the impact of riluzole therapy on circulating brain derived neuropathic factor (BDNF) levels in cancer survivors (recently completing prior treatment regimens) or patients who have received whole bra…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Chao Family Comprehensive Cancer Center, University of California Irvine, Orange, California
- Run by
- University of California, Irvine
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Pre-malignant States to Hematologic Malignancies in Firefighters
The purpose of the study is to evaluate if firefighter exposure to hazardous compounds will increase the incidence of premalignant hematological states which subsequently increases the risk of the development of hematologic malignancies, and potentially other pathophysiological consequences.
- Stage
- Not phased
- Ages
- 40 to 49
- Site
- Levine Cancer Institute, Charlotte, North Carolina
- Run by
- Wake Forest University Health Sciences
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Preliminary Safety and Tolerability of CD19x22 CAR T Cells in Adolescent and Adult R/R B-NHL Patients
This open-label, single arm phase 1 trial aims to determine the safety and tolerability of anti-CD19 and anti-CD22 chimeric antigen receptor-expressing (CAR) T cells (CD19x22 CAR T) in adolescents and adults with relapsed/refractory (R/R) B-cell Non-Hodgkin Lymphoma (B-NHL). This trial will determi…
- Stage
- Phase 1
- Ages
- 16 and older
- Site
- University of Colorado Hospital, Aurora, Colorado
- Run by
- University of Colorado, Denver
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A Multicenter Access and Distribution Protocol for Unlicensed Cryopreserved Cord Blood Units (CBUs)
This study is an access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) in pediatric and adult patients with hematologic malignancies and other indications.
- Stage
- Not phased
- Ages
- Any age
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 142 in total
- Run by
- Center for International Blood and Marrow Transplant Research
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Halt Aging in Survivors of Blood Cancers
Older survivors of blood cancer are at a high risk of accelerated biological aging, which increases their risk of developing multiple aging-related conditions. Whereas physical exercise can improve overall health, older cancer survivors do not meet the recommended physical activity, highlighting th…
- Stage
- Not phased
- Ages
- 50 and older
- Site
- University of Nebraska Medical Center, Omaha, Nebraska
- Run by
- University of Nebraska
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Study of Cytokine Release Syndrome Prophylaxis and Treatment With Siltuximab Prior to Epcoritamab
The goal of this clinical trial is to is to determine the safety, feasibility and efficacy of siltuximab prophylaxis of cytokine release syndrome and neurotoxicity occurring after epcoritamab subcutaneous administration for participants with large b-cell lymphoma (DLBCL) or follicular lymphoma (FL)…
- Stage
- Phase 1
- Ages
- 18 to 65
- Site
- Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center, Cleveland, Ohio
- Run by
- Taylor Brooks
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.