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 Leukemia from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 25
- Active, not recruiting: 7
- Completed: 4
- Other: 14
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
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…
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…
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 …
NCT01905826 — Natural History Study of GATA2 Deficiency and Related Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 600 |
| Study Type | OBSERVATIONAL |
| Conditions | GATA2 Deficiency |
Background:
- GATA2 deficiency is a genetic disorder that can cause problems with a person s immune system and other body systems. Some people who have this disorder develop few problems from it. Others can have a wide range of health problems, from skin problems, to hearing loss, to cancer. These problems can happen at any age. Researchers want to study GATA2 deficiency to better understand …
NCT01804686 — A Long-term Extension Study of PCI-32765 (Ibrutinib)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 700 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma; Mantle Cell Lymphoma; Follicular Lymphoma; Diffuse Large B-cell Lymphoma |
| Interventions |
The purpose of this study is to collect long-term safety and efficacy data for participants treated with ibrutinib and to provide ongoing access to ibrutinib for participants who are currently enrolled in ibrutinib studies that have been completed according to the parent protocol, are actively receiving treatment with ibrutinib, and who continue to benefit from ibrutinib treatment.
NCT02390752 — Phase I Trial of TURALIO(R) (Pexidartinib, PLX3397) in Children and Young Adults With Refractory Leukemias and Refractory Solid Tumors Including Neurofibromatosis Type 1 (NF1) Associated Plexiform Neurofibromas (PN) and Tenosynovial Giant Cell Tumor …
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 54 |
| Study Type | INTERVENTIONAL |
| Conditions | Neurofibroma, Plexiform; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Leukemia, Promyelocytic, Acute; Sarcoma |
| Interventions |
Background:
- Some people with cancer have solid tumors. Others have refractory leukemia. This may not go away after treatment. Researchers want to see if a drug called TURALIO(R) can shrink tumors or stop them from growing.
Objectives:
- To find the highest safe dose and side effects of TURALIO(R). To see if it helps treat certain types of cancer.
Eligibility:
- People ages 3-35 with a…
NCT03810196 — CD45RA Depleted Peripheral Stem Cell Addback for Viral or Fungal Infections Post TCRαβ/CD19 Depleted HSCT
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Leukemia; Acute Myeloid Leukemia; Myelodysplastic Syndromes; Acute Lymphoblastic Leukemia; Mixed Lineage Leukemia |
| Interventions |
The major morbidities of allogeneic hematopoietic stem cell transplant with non-human leukocyte antigen (HLA) matched siblings are graft vs host disease (GVHD) and life threatening infections. T depletion of the donor hematopoietic stem cell graft is effective in preventing GVHD, but immune reconstitution is slow, increasing the risk of infections. An addback of donor CD45RA (naive T cells) dep…
NCT03934372 — Safety and Efficacy of Ponatinib for Treatment of Pediatric Recurrent or Refractory Leukemias, Lymphomas or Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Incyte Biosciences International Sàrl |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myeloid Leukemia; Accelerated Phase Chronic Myeloid Leukemia; Blast Phase Chronic Myeloid Leukemia; Chronic Phase Chronic Myeloid Leukemia; Acute Lymphoblastic Leukemia |
| Interventions |
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and efficacy of ponatinib in children aged 1 to < 18 years with advanced leukemias, lymphomas, and solid tumors.
NCT04269902 — Testing Early Treatment for Patients With High-Risk Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Leukemia (SLL), EVOLVE CLL/SLL Study
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 247 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma |
| Interventions | ; ; |
This phase III trial compares early treatment with venetoclax and obinutuzumab versus delayed treatment with venetoclax and obinutuzumab in patients with newly diagnosed high-risk chronic lymphocytic leukemia or small lymphocytic lymphoma. Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein need…
NCT04588922 — Study of SLS009 (Formerly GFH009) a Potent Highly Selective CDK9 Inhibitor in Patients With Hematologic Malignancies and High-Risk Newly Diagnosed AML
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Sellas Life Sciences Group |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Hematologic Malignancies |
| Interventions | ; ; |
SLS009 (formerly GFH009) is a potent and highly selective CDK9 inhibitor. In this study the safety, tolerability, and antitumor activity of single agent SLS009 are assessed in two dose escalation groups (Group 1 in patients with relapsed/refractory AML, Group 2 in patients with relapse/refractory lymphoma/CLL/SLL). The safety, tolerability, and antitumor activity of SLS009 in combination with v…
NCT05270200 — Single Arm Study of Post-transplant Azacitidine and Chidamide for Prevention of Acute Myelogenous Leukemia Relapse
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Zhujiang Hospital |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Leukemia, Myeloid, Acute |
| Interventions | ; |
The goal of this clinical research study is to learn if azacitidine combined with Chidamide will help to control the disease in patients with high-risk AML after an allogeneic stem cell transplant. The safety of this combination will also be studied.
NCT05564390 — MYELOMATCH: A Screening Study to Assign People With Myeloid Cancer to a Treatment Study or Standard of Care Treatment Within myeloMATCH (MyeloMATCH Screening Trial)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 2000 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myeloid Leukemia; Acute Myeloid Leukemia Arising From Previous Myelodysplastic/Myeloproliferative Neoplasm; Acute Myeloid Leukemia Post Cytotoxic Therapy; Acute Myeloid Leukemia, Myelodysplasia-Related; Myelodysplastic Syndrome |
| Interventions | ; ; |
This MyeloMATCH Master Screening and Reassessment Protocol (MSRP) evaluates the use of a screening tool and specific laboratory tests to help improve participants’ ability to register to clinical trials throughout the course of their myeloid cancer (acute myeloid leukemia or myelodysplastic syndrome) treatment. This study involves testing patients’ bone marrow and blood for certain biomarkers. …
NCT06960993 — Mosaic Trial for Stem Cell Transplant Recipients
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Northwestern University |
| Enrollment | 356 |
| Study Type | INTERVENTIONAL |
| Conditions | Hematologic Malignancy; Stem Cell Transplant; Bone Marrow Transplant; Leukemia; Lymphoma |
| Interventions | ; |
The goal of this clinical trial is to learn if using an intervention website (Mosaic) improves selected patient-reported outcomes in adult blood cancer patients undergoing allogeneic or autologous stem cell transplant, compared to using an educational website (control group). Patients will be recruited prior to their scheduled transplant, then randomized to use one of these two study websites t…
NCT06124157 — A Study Testing the Combination of Dasatinib or Imatinib to Chemotherapy Treatment With Blinatumomab for Children, Adolescents, and Young Adults With Philadelphia Chromosome Positive (Ph+) or ABL-Class Philadelphia Chromosome-Like (Ph-Like) B-cell Acute Lymphoblastic Leukemia (B-ALL)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 222 |
| Study Type | INTERVENTIONAL |
| Conditions | B Acute Lymphoblastic Leukemia |
| Interventions | ; ; |
This pilot trial assesses the effect of the combination of blinatumomab with dasatinib or imatinib and standard chemotherapy for treating patients with Philadelphia chromosome positive (Ph+) or ABL-class Philadelphia chromosome-like (Ph-like) B-Cell acute lymphoblastic leukemia (B-ALL). Blinatumomab is a bispecific antibody that binds to two different proteins-one on the surface of cancer cells…
NCT06317662 — Testing the Addition of the Anti-cancer Drug Venetoclax and/or the Anti-cancer Immunotherapy Blinatumomab to the Usual Chemotherapy Treatment for Infants With Newly Diagnosed KMT2A-rearranged or KMT2A-non-rearranged Leukemia
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 153 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Leukemia of Ambiguous Lineage; B Acute Lymphoblastic Leukemia |
| Interventions | ; ; |
This phase II trial tests the addition of venetoclax and/or blinatumomab to usual chemotherapy for treating infants with newly diagnosed acute lymphoblastic leukemia (ALL) with a KMT2A gene rearrangement (KMT2A-rearranged [R]) or without a KMT2A gene rearrangement (KMT2A-germline [G]). Venetoclax is in a class of medications called B-cell lymphoma-2 (Bcl-2) inhibitors. It may stop the growt…
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…
NCT05237986 — Cognitive Aftereffects of Neurotoxicity in Children and Young Adults With Relapsed/Refractory Hematologic Malignancies Who Receive CAR T-cell Therapy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Lymphoma; Leukemia |
Background:
CAR T-cell therapy is a promising new treatment for blood cancers. During treatment, a person s T-cells are genetically changed to kill cancer cells. Researchers want to learn more about the effects of potential problems that may be associated with this treatment. We are specifically interested in learning if and how this treatment may affect the brain or your thinking skills.
Obj…
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…
NCT07549516 — A Study on the Tolerability, Safety and Effectiveness of Asciminib in Patients With Philadelphia Chromosome-positive Chronic Myeloid Leukemia in the Chronic Phase in Germany
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 380 |
| Study Type | OBSERVATIONAL |
| Conditions | Leukemia, Chronic Myeloid |
The aim of this study is to assess the real-world effectiveness of asciminib in Philadelphia chromosome-positive chronic myeloid leukemia in chronic phase (Ph+ CML-CP) patients who were either newly diagnosed or previously treated with one ATP-competitive tyrosine kinase inhibitor (TKI).
NCT07020533 — 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
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | City of Hope Medical Center |
| Enrollment | 46 |
| Study Type | INTERVENTIONAL |
| Conditions | Accelerated Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive; Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Chronic Lymphocytic Leukemia; Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive |
| Interventions | ; ; |
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 cell transplantation (haploHCT) has advanced to become the predominant procedure for patients lacking…
NCT07464951 — CART123 Cells With or Without Ruxolitinib in Relapsed/Refractory Acute Myeloid Leukemia
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Stephan Grupp MD PhD |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myeloid Leukemia (AML) |
| Interventions | ; |
This study is designed to evaluate the safety and effectiveness of CART123 cells either alone or when combined with ruxolitinib in pediatric and young adult subjects with relapsed or refractory AML. Subjects will be enrolled into one of two treatment cohorts: subjects who will receive CART123 alone (Cohort A) or subjects who will receive CART123 in combination with ruxolitinib (Cohort B).
NCT06904066 — Autologous T Cells Transduced With Retroviral Vectors Expressing TCRs for Participant-specific Neoantigens in Patients With Hematologic Malignancies
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 86 |
| Study Type | INTERVENTIONAL |
| Conditions | Malignancy, Hematologic; Neoplasms, Hematologic; Neoplasms, Hematopoietic; Blood Cancer; Hematological Neoplasms |
| Interventions | ; ; |
Background:
Blood cancers (such as leukemias) can be hard to treat, especially if they have mutations in the TP53 or RAS genes. These mutations can cause the cancer cells to create substances called neoepitopes. Researchers want to test a method of treating blood cancers by altering a person s T cells (a type of immune cell) to target neoepitopes.
Objective:
To test the use of neoepitope-spe…
NCT05621291 — A Multicenter Study to Evaluate Next-Generation Sequencing (NGS) Testing and Monitoring of B-Cell Recovery to Guide Management Following Chimeric Antigen Receptor T-cell (CART) Induced Remission in Children and Young Adults With B Lineage Acute Lymph…
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | B-All; Acute Lymphoblastic Leukemia |
| Interventions |
Background:
Chimeric antigen receptor T-cell (CART) therapy is a form of immunotherapy which can be used to treat people with relapsed B-ALL. For those who achieve remission after CART alone, it may cure up to 50% of people who receive this therapy. However, for people who relapse after CART, it can be hard to achieve remission again. In patients where CART fails, stem cell transplant (HCT) ca…
NCT07094750 — Randomization for the Identification of Best Treatment Intensity for Less Fit Adults With Acute Myeloid Leukemia and Myeloid Neoplasms
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fred Hutchinson Cancer Center |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Leukemia of Ambiguous Lineage; Acute Myeloid Leukemia; Myeloid Neoplasm |
| Interventions | ; ; |
This clinical trial studies whether less fit adults with acute myeloid leukemia (AML) or myeloid neoplasms are willing to let a computer program decide (randomization) whether they receive lower- or higher-intensity chemotherapy. Historically, treatment decision-making for patients with AML or myeloid neoplasms has divided patients into two categories, with patients considered fit receiving int…
NCT06917911 — Testing the Addition of Venetoclax or Gemtuzumab Ozogamicin (GO) to Usual Treatment Regimen (Cytarabine and Daunorubicin, “7+3”) for Core Binding Factor Acute Myeloid Leukemia (CBF-AML) to Improve Response (A MYELOMATCH Treatment Trial)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 162 |
| Study Type | INTERVENTIONAL |
| Conditions | Core Binding Factor Acute Myeloid Leukemia |
| Interventions | ; ; |
This phase II MYELOMATCH treatment trial compares the effect of venetoclax to gemtuzumab ozogamicin, when given with cytarabine and daunorubicin (“7+3” regimen), for the treatment of patients with core binding factor acute myeloid leukemia (CBF-AML). Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a p…
Active, Not Recruiting
NCT01861314 — Bortezomib, Sorafenib Tosylate, and Decitabine in Treating Patients With Acute Myeloid Leukemia
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myeloid Leukemia; Acute Myeloid Leukemia Post Cytotoxic Therapy; Recurrent Adult Acute Myeloid Leukemia; Secondary Acute Myeloid Leukemia |
| Interventions | ; ; |
This phase I trial studies the side effects and the best dose of bortezomib and sorafenib tosylate when given together with decitabine in treating patients with acute myeloid leukemia. Bortezomib and sorafenib tosylate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as decitabine, work in different ways to stop the gro…
NCT02935361 — Guadecitabine and Atezolizumab in Treating Patients With Advanced Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia That Is Refractory or Relapsed
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | University of Southern California |
| Enrollment | 33 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Myelomonocytic Leukemia; Myelodysplastic Syndrome; Recurrent Acute Myeloid Leukemia With Myelodysplasia-Related Changes |
| Interventions | ; |
This phase I/II trial studies the side effects and best dose of guadecitabine when given together with atezolizumab and to see how well they work in treating patients with myelodysplastic syndrome or chronic myelomonocytic leukemia that has spread to other places in the body and has come back or does not respond to treatment. Guadecitabine may stop the growth of cancer cells by blocking some of…
NCT03625037 — First-in-Human (FIH) Trial in Patients With Relapsed, Progressive or Refractory B-Cell Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Genmab |
| Enrollment | 666 |
| Study Type | INTERVENTIONAL |
| Conditions | DLBCL; High-grade B-cell Lymphoma (HGBCL); Primary Mediastinal Large B-cell Lymphoma (PMBCL); FL; MCL |
| Interventions |
The purpose of this trial is to measure the following in participants with relapsed and/or refractory B-cell lymphoma who receive epcoritamab, an antibody also known as EPKINLY™ and GEN3013 (DuoBody®-CD3xCD20):
- The dose schedule for epcoritamab
- The side effects seen with epcoritamab
- What the body does with epcoritamab once it is administered
- What epcoritamab does to the body once it is…
NCT03914625 — A Study to Investigate Blinatumomab in Combination With Chemotherapy in Patients With Newly Diagnosed B-Lymphoblastic Leukemia
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6720 |
| Study Type | INTERVENTIONAL |
| Conditions | B Acute Lymphoblastic Leukemia; B Lymphoblastic Lymphoma; Down Syndrome |
| Interventions | ; ; |
This phase III trial studies how well blinatumomab works in combination with chemotherapy in treating patients with newly diagnosed, standard risk B-lymphoblastic leukemia or B-lymphoblastic lymphoma with or without Down syndrome. Monoclonal antibodies, such as blinatumomab, may induce changes in the body’s immune system and may interfere with the ability of cancer cells to grow and spread. Che…
NCT04623541 — Safety and Efficacy Study of Epcoritamab in Subjects With Relapsed/Refractory Chronic Lymphocytic Leukemia and Richter’s Syndrome
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Genmab |
| Enrollment | 194 |
| Study Type | INTERVENTIONAL |
| Conditions | Relapsed/Refractory Chronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma; Richter’s Syndrome; Treatment-naïve High Risk Chronic Lymphocytic Leukemia |
| Interventions | ; ; |
The study is a global, multi-center safety and efficacy trial of epcoritamab, an antibody also known as EPKINLY™ and GEN3013 (DuoBody®-CD3xCD20). Epcoritamab will be tested either in
Relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) as:
Monotherapy, or
Combination therapy:
- epcoritamab + venetoclax
- epcoritamab + pirtobrutinib
In Non-United States (US) Participants Only…
NCT04530565 — Testing the Use of Steroids and Tyrosine Kinase Inhibitors With Blinatumomab or Chemotherapy for Newly Diagnosed BCR-ABL-Positive Acute Lymphoblastic Leukemia in Adults
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 348 |
| Study Type | INTERVENTIONAL |
| Conditions | B Acute Lymphoblastic Leukemia With t(9;22)(q34.1;q11.2); BCR-ABL1 |
| Interventions | ; ; |
This phase III trial compares the effect of usual treatment of chemotherapy and steroids and a tyrosine kinase inhibitor (TKI) to the same treatment plus blinatumomab. Blinatumomab is a Bi-specific T-Cell Engager (‘BiTE’) that may interfere with the ability of cancer cells to grow and spread. The information gained from this study may help researchers determine if combination therapy with stero…
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
NCT07570056 — Use of Electrical Bioimpedance in Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS) Patients (Bioimpedance)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Utah |
| Enrollment | 25 |
| Study Type | OBSERVATIONAL |
| Conditions | Myelodysplastic Syndromes; Acute Myeloid Leukemia |
| Interventions |
The goal of this project is to test non-invasive, painless skin electrical bioimpedance (BioZ) measurements as an adjunctive biomarker to standard bone marrow biopsies.
NCT07524530 — Stem Cell Transplantation for Participants With Germline RUNX1 Associated Blood Cancers
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 98 |
| Study Type | INTERVENTIONAL |
| Conditions | Core Binding Factor Alpha Subunits; Hematologic Neoplasms; Leukemia; Lymphoma |
| Interventions | ; ; |
Background:
Some blood cancers can be caused by germline variants (changes) in a person s RUNX1 gene. Germline variants are genetic inherited changes a person is born with. Stem cell transplants are used to treat many diseases including blood cancers. Stem cell transplantation for patients with germline RUNX1 mutation driven blood cancers is standard of care and available in most major medical…
NCT07572136 — Anti-CRLF2-R/TSLPR Chimeric Antigen Receptor T Cells (TSLPR-CART) in Participants With Recurrent or Refractory CRLF2-R/TSLPR-Overexpressing B-Cell Acute Lymphoblastic Leukemia (B-ALL)
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 57 |
| Study Type | INTERVENTIONAL |
| Conditions | B-All; Acute Lymphoblastic Leukemia |
| Interventions | ; ; |
Background:
B-cell acute lymphoblastic leukemia (B-ALL) is a type of blood cancer. Some people with B-ALL have a gene mutation that makes the disease hard to treat. The mutation causes cancer cells to make too much of a protein called thymic stromal lymphopoietin receptor (TSLPR). Chimeric antigen receptor (CAR) T cell therapy is a treatment that takes immune cells (T cells) from a person s bo…
NCT07691047 — Reassessment of the Risk of Hemolytic Syndrome in Patients With Chronic Lymphocytic Leukemia Treated With a Regimen Containing Venetoclax
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Private Hospital of Confluent, France |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Lymphoid Leukemia |
| Interventions |
Chronic lymphocytic leukemia is a malignant blood disorder characterized by the proliferation of abnormal B lymphocytes in the blood, lymph nodes, and bone marrow. It generally occurs after age 70 and is the fourth most common blood cancer in France, following multiple myeloma, diffuse large B-cell lymphoma, and myelodysplastic syndromes.
Treatments have advanced since 2015 with the introducti…
NCT07686965 — Lisaftoclax Plus Azacitidine Maintenance After Allogeneic Hematopoietic Stem Cell Transplantation in Acute Myeloid Leukemia Patients at High Risk of Relapse
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | Institute of Hematology & Blood Diseases Hospital, China |
| Enrollment | 191 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myeloid Leukemia (AML); Maintenance Treatment; Hematopoetic Stem Cell Transplantation |
| Interventions |
This study evaluates the efficacy and safety of maintenance therapy with lisaftoclax plus azacitidine after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in adults with acute myeloid leukemia (AML) at high risk of relapse.
The main questions this study aims to answer are:
- Does maintenance therapy with lisaftoclax plus azacitidine improve disease-free survival compared with …
NCT07225439 — Rituximab (Rtx) + Tafasitamab in Combination With Allogeneic NK Cells for Treatment of Relapsed/Refractory (r/r) B-cell Non-Hodgkin Lymphoma (NHL)
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Paolo Caimi, MD |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Non Hodgkin Lymphoma; B-cell Non Hodgkin Lymphoma; Diffuse Large B Cell Lymphoma; High-grade B-cell Lymphoma; Primary Mediastinal Large B Cell Lymphoma |
| Interventions | ; ; |
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 the treatment of relapsed or refractory B-cell non-Hodgkin’s lymphoma.
NK cells are an investigat…
NCT06050850 — Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Kansas Medical Center |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | ALL, Childhood; Behavior, Health |
| Interventions |
The purpose of this study is to conduct a single arm pilot of the NOURISH-ALL (Nourishing Our Understanding of Role modeling to Improve Support and Health in Acute Lymphoblastic Leukemia) intervention focused on three components of participant engagement. This is a single arm intervention study that involves participation in a 6-session family intervention and three time points of multimethod d…
NCT07690891 — Nemtabrutinib With Venetoclax and Obinutuzumab in Patients With Chronic Lymphocytic Leukemia
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Medical College of Wisconsin |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Lymphocytic Leukemia |
| Interventions | ; ; |
This is a single-arm, open-label Phase 2 study designed to evaluate the treatment outcomes of nemtabrutinib-venetoclax-obinutuzumab as a frontline management for chronic lymphocytic leukemia (CLL).
Enrolling by Invitation
NCT02473757 — Gene Therapy Follow-up Protocol for People Previously Enrolled in CAR-T Cell Studies
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Lyphoma, B-Cell; Leukemia, B-cell; Multiple Myeloma; Hematologic Malignancies |
Background:
- Gene therapy is a way to treat or prevent disease using genes. It is monitored very closely by regulators because there can be long-term, unexpected side effects. NIH is required to try to contact people who have been treated with gene therapy at least annually for up to 15 years. This is to see if they have had any bad side effects. This trial does not include any therapy and i…
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.
NCT07328516 — Natural History Study of Early Life Exposures in Agriculture (ELEA)
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 64277 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer; Leukemia; Breast Cancer; Melanoma; Colorectal Cancer |
Study Description:
ELEA is an observational cohort study that will collect exposure information and biospecimens from the adult children of the Agricultural Health Study (AHS) cohort (https://aghealth.nih.gov/about; Protocol OH93NCN013).
The primary hypothesis is that early life exposures, particularly those found in the agricultural environment, are associated with cancer and other adverse h…
Completed Trials
NCT00342888 — Case-Control Study of Pesticides and Childhood Leukemia
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 629 |
| Study Type | OBSERVATIONAL |
| Conditions | Leukemia |
Childhood leukemia is the most common type of childhood cancer and its etiology is largely unknown. Most case-control studies of childhood leukemia have reported elevated risks among children whose parents were occupationally exposed to pesticides or who used pesticides in the home or garden. Investigators at the University of California at Berkeley (UCB) conducted a case-control study of child…
NCT00720785 — Natural Killer Cells and Bortezomib to Treat Cancer
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Myeloid Leukemia (CML); Pancreatic Ca; Colon/Rectal Ca; Multiple Myeloma; Carcinoma, Non-Small -Cell Lung |
| Interventions | ; |
Natural killer (NK) cells are white blood cells that have a limited ability to kill cancer cells. This ability might be enhanced if they are given 24 hours after an injection of the drug bortezomib. This study will determine the following:
- What dose of NK cells can be given safely to subjects with metastatic solid tumors or leukemia.
- The effectiveness and side effects of NK cell therapy
- …
NCT01139476 — Specimen Collection for Agricultural Health Study Cohort Pesticide Exposure Study
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1892 |
| Study Type | OBSERVATIONAL |
| Conditions | Multiple Myeloma; Leukemia; MGUS; Monoclonal B-Cell Lymphocytosis |
Background:
- Multiple myeloma (MM), a type of cancer that affects the white blood cells, is often preceded by a precancerous disorder known as monoclonal gammopathy of undetermined significance (MGUS). Farmers and other agricultural workers have a higher risk of developing MGUS and MM, possibly because of their exposure to certain pesticides. Researchers are interested in studying biological…
NCT06182163 — Reduce Sedentary Time in Acute Lymphoblastic Leukemia
| Status | Completed |
| Phase | N/A |
| Sponsor | Children’s Hospital Los Angeles |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Lymphoblastic Leukemia (ALL) |
| Interventions |
The goal of this feasibility trial is to test if a mobile health intervention, including a wearable fitness tracker with inactivity-triggered reminders to move, individualized coaching sessions, and an app-based peer support group, can decrease sedentary time (time spent sitting/lying down and inactive) in adolescents and young adults (AYAs) with acute lymphoblastic leukemia (ALL) receiving mai…
Available Studies
NCT03145545 — Expanded Access Protocol Using Alpha/Beta T and CD19+ Depleted PBSC
| Status | Available |
| Phase | N/A |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | N/A |
| Study Type | EXPANDED_ACCESS |
| Conditions | Leukemia; Bone Marrow Failure Syndrome; Immunodeficiencies |
| Interventions |
The primary objective of this protocol is to expand access for patients who lack a fully HLA (Human leukocyte antigen) matched sibling donor, and who are candidates for allogeneic hematopoietic stem cell transplant (HSCT). These patients have a serious or immediately life-threatening disease for which HSCT is indicated. These patients are not eligible for other Children’s Hospital of Philadelph…
Other (Suspended)
NCT05672251 — Loncastuximab Tesirine and Mosunetuzumab for the Treatment of Relapsed or Refractory Diffuse Large B-Cell Lymphoma
| Status | Suspended |
| Phase | Phase 2 |
| Sponsor | City of Hope Medical Center |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Diffuse Large B-Cell Lymphoma; Recurrent Grade 3b Follicular Lymphoma; Recurrent High Grade B-Cell Lymphoma; Recurrent Primary Mediastinal (Thymic) Large B-Cell Lymphoma; Recurrent Transformed Chronic Lymphocytic Leukemia |
| Interventions | ; ; |
This phase II trial studies the safety and how well of loncastuximab tesirine when given together with mosunetuzumab works in treating patients with diffuse large B-cell lymphoma that has come back (relapsed) or does not respond to treatment (refractory). Loncastuximab tesirine is a monoclonal antibody, loncastuximab, linked to a toxic agent called tesirine. Loncastuximab attaches to anti-CD19 …
NCT07388563 — Azacitidine and Abatacept in Relapsed or Refractory T-Cell Lymphoma
| Status | Suspended |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Lymphoma, T Cell, Peripheral; T-cell Lymphoma; Angioimmunoblastic T-cell Lymphoma; Anaplastic Large Cell Lymphoma; Monomorphic Epitheliotropic Intestinal T-cell Lymphoma |
| Interventions | ; |
Background:
T-cell lymphoma is a blood cancer that affects immune system cells. People tend to survive less than 1 year if this disease does not respond to treatment (is refractory) or comes back after treatment (relapses). Azacitidine and abatacept are 2 drugs that are used to treat other diseases. Researchers want to know if these drugs, used together, can help people with T-cell lymphoma.
…