Mixed Phenotype Acute Leukemia Clinical Trials
19 studies are recruiting for mixed phenotype acute leukemia 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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A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 Mutation
Phase 1 dose escalation will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of revumenib in participants with acute leukemia. In Phase 2, participants will be enrolled in 4 indication-specific expansion cohorts to determine the efficacy, short- and long-term safety, …
- Stage
- Phase 1
- Ages
- 0 and older
- Site
- University of Colorado, Aurora, Colorado
- Locations
- 57 in total
- Run by
- Syndax Pharmaceuticals
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Phase I/II Trial: Engineered Donor Graft (Orca Q) for Pediatric Hematopoietic Cell Transplant (HCT)
This is a first in children prospective study of allogeneic hematopoietic cell transplant using a centrally manufactured engineered donor graft (Orca-Q). The study will assess safety and efficacy of Orca-Q in pediatric patients with hematologic malignancies.
- Stage
- Phase 1
- Ages
- Up to 50
- Site
- University of Florida, Gainesville, Florida
- Locations
- 4 in total
- Run by
- University of Florida
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Inotuzumab Ozogamicin and Post-Induction Chemotherapy in Treating Patients With High-Risk B-ALL, Mixed Phenotype Acute Leukemia, and B-LLy
This phase III trial studies whether inotuzumab ozogamicin added to post-induction chemotherapy and immunotherapy (chemo-immunotherapy) for patients with High-Risk B-cell Acute Lymphoblastic Leukemia (B-ALL) improves outcomes. Inotuzumab ozogamicin is a monoclonal antibody, which is a type of prote…
- Stage
- Phase 3
- Ages
- 1 to 25
- Site
- Children's Hospital of Alabama, Birmingham, Alabama
- Locations
- 231 in total
- Run by
- Children's Oncology Group
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The Pediatric Acute Leukemia (PedAL) Screening Trial - A Study to Test Bone Marrow and Blood in Children With Leukemia That Has Come Back After Treatment or Is Difficult to Treat - A Leukemia & Lymphoma Society and Children's Oncology Group Study
This study aims to use clinical and biological characteristics of acute leukemias to screen for patient eligibility for available pediatric leukemia sub-trials. Testing bone marrow and blood from patients with leukemia that has come back after treatment or is difficult to treat may provide informat…
- Stage
- Phase 1
- Ages
- Up to 22
- Site
- Children's Hospital of Alabama, Birmingham, Alabama
- Locations
- 184 in total
- Run by
- PedAL BCU, LLC
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Adding Dasatinib Or Venetoclax To Improve Responses In Children With Newly Diagnosed T-Cell Acute Lymphoblastic Leukemia (ALL) Or Lymphoma (T-LLY) Or Mixed Phenotype Acute Leukemia (MPAL)
This is a clinical trial testing whether the addition of one of two chemotherapy agents, dasatinib or venetoclax, can improve outcomes for children and young adults with newly diagnosed T-cell acute lymphoblastic leukemia and lymphoma or mixed phenotype acute leukemia. Primary Objective * To evalua…
- Stage
- Phase 2
- Ages
- 1 to 18
- Site
- Rady Children's Hospital, San Diego, California
- Locations
- 4 in total
- Run by
- St. Jude Children's Research Hospital
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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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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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Identification of Necessary Information for Treatment Induction in Newly Diagnosed Acute Lymphoblastic Leukemia/Lymphoma
The goal of this study is to provide sufficient therapy during the time a patients' B-cell Acute Lymphoblastic Leukemia (ALL) or Lymphoblastic Lymphoma (LLy) risk category is being determined. The term "risk" refers to the chance of the ALL or LLy coming back after treatment. Primary Objectives * T…
- Stage
- Phase 4
- Ages
- 1 to 18
- Site
- Rady Children's Hospital, San Diego, California
- Locations
- 5 in total
- Run by
- St. Jude Children's Research Hospital
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Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome
This study will evaluate the safety, tolerability, and efficacy of Orca-T in participants undergoing reduced intensity or non-myeloablative allogeneic hematopoietic cell transplantation (alloHCT) for hematologic malignancies. Orca-T is an allogeneic stem cell and T-cell immunotherapy biologic manuf…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- UCLA Department of Medicine, Los Angeles, California
- Locations
- 6 in total
- Run by
- Orca Biosystems, Inc.
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A Phase 1 Study of Orca-Q in Recipients Undergoing Allogeneic Transplantation for Hematologic Malignancies
This study will evaluate the safety, tolerability, and efficacy of engineered donor grafts ("OrcaGraft"/"Orca-Q") in participants undergoing allogeneic hematopoietic cell transplant (alloHCT) transplantation for hematologic malignancies.
- Stage
- Phase 1
- Ages
- 12 to 78
- Site
- City of Hope, Duarte, California
- Locations
- 12 in total
- Run by
- Orca Biosystems, Inc.
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Trial for Patients w/ Advanced Hematologic Malignancies Undergoing Allogeneic HCT
The study goal is to characterize the safety of the combination of Orca-T with dual agent GVHD prophylaxis.
- Stage
- Phase 1
- Ages
- 18 to 70
- Site
- Stanford University, Palo Alto, California
- Run by
- Stanford University
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211^At-BC8-B10 Before Donor Stem Cell Transplant in Treating Patients With High-Risk Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Myelodysplastic Syndrome, or Mixed-Phenotype Acute Leukemia
This phase I/II trial studies the side effects and best dose of 211\^astatine(At)-BC8-B10 before donor stem cell transplant in treating patients with high-risk acute myeloid leukemia, acute lymphoblastic leukemia, myelodysplastic syndrome, or mixed-phenotype acute leukemia. Radioactive substances, …
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington
- Run by
- Fred Hutchinson Cancer Center
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A Study of Revumenib and Mezigdomide in People With Leukemia
The purpose of this study is to find out whether the combination of mezigdomide and revumenib is a safe treatment for people with relapsed or refractory KMT2A-r, NUP98-r, and NPM1-m acute leukemias.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Memorial Sloan Kettering at Basking Ridge (All Protocol Activities), Basking Ridge, New Jersey
- Locations
- 10 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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Donor Stem Cell Transplant With Treosulfan, Fludarabine, and Total-Body Irradiation for the Treatment of Hematological Malignancies
This phase II trial studies how well a donor stem cell transplant, treosulfan, fludarabine, and total-body irradiation work in treating patients with blood cancers (hematological malignancies). Giving chemotherapy and total-body irradiation before a donor stem cell transplant helps stop the growth …
- Stage
- Phase 2
- Ages
- 0 and older
- Site
- Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington
- Run by
- Fred Hutchinson Cancer Center
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HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant
This phase I trial studies the side effects and best dose of CD4+ and CD8+ HA-1 T cell receptor (TCR) (HA-1 T TCR) T cells in treating patients with acute leukemia that persists, has come back (recurrent) or does not respond to treatment (refractory) following donor stem cell transplant. T cell rec…
- Stage
- Phase 1
- Ages
- Up to 80
- Site
- Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington
- Run by
- Fred Hutchinson Cancer Center
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Chemotherapy (Decitabine in Combination With FLAG-Ida) and Total-Body Irradiation Followed by Donor Stem Cell Transplant for the Treatment of Adults With Myeloid Malignancies at High Risk of Relapse
This phase I/II trial studies the safety, side effects, and best dose of decitabine in combination with fludarabine, cytarabine, filgrastim, and idarubicin (FLAG-Ida) and total body irradiation (TBI) followed by a donor stem cell transplant in treating adult patients with cancers of blood-forming c…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington
- Run by
- Fred Hutchinson Cancer Center
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Venetoclax and CLAG-M for the Treatment of Acute Myeloid Leukemia and High-Grade Myeloid Neoplasms
This phase I/II trial finds the best dose, side effects and how well giving venetoclax in combination with cladribine, cytarabine, granulocyte colony-stimulating factor, and mitoxantrone (CLAG-M) in treating patients with acute myeloid leukemia and high-grade myeloid neoplasms. Venetoclax may stop …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington
- Run by
- University of Washington
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Pharmacokinetic and Safety Study of MRX-2843 in Adolescents and Adults With Relapsed/Refractory AML, ALL, or MPAL
This is a Phase I, open-label, non-randomized, dose escalation study in adolescents and adults with relapsed/refractory acute myeloid leukemia, acute lymphoblastic leukemia, or mixed phenotype acute leukemia. Patients will receive continuous oral MRX-2843 in 28 day cycles at predefined dose cohorts.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Emory University - WINSHIP Cancer Center, Atlanta, Georgia
- Locations
- 3 in total
- Run by
- Meryx, Inc.
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Tagraxofusp in Pediatric Patients With Relapsed or Refractory CD123 Expressing Hematologic Malignancies
Tagraxofusp is a protein-drug conjugate consisting of a diphtheria toxin redirected to target CD123 has been approved for treatment in pediatric and adult patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN). This trial aims to examine the safety of this novel agent in pediatric patie…
- Stage
- Phase 1
- Ages
- 1 to 21
- Site
- Children's Hospital Los Angeles, Los Angeles, California
- Locations
- 31 in total
- Run by
- Therapeutic Advances in Childhood Leukemia Consortium
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.