AML Clinical Trials
19 studies are recruiting for aml 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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CER-1236 in Patients With Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS), and Myelofibrosis (MF)
This is a first in human, multi center, open label, phase 1/1b study to evaluate the safety and preliminary efficacy of CER-1236 in patients with relapsed/refractory (R/R), measurable residual disease (MRD) positive acute myeloid leukemia (AML), or TP53mut disease.
- Stage
- Phase 1
- Ages
- 18 to 85
- Site
- University of California, Davis Comprehensive Cancer Center, Sacramento, California
- Locations
- 5 in total
- Run by
- CERo Therapeutics Holdings, Inc.
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Pilot Study of Memory-like Natural Killer (ML NK) Cells After TCRαβ T Cell Depleted Haploidentical Transplant in AML
This trial represents a single institution phase I/II pilot study with the primary objective of establishing the safety and feasibility of generating and infusing ML NK cells after TCRαβ haplo-HCT.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Washington University School of Medicine, St Louis, Missouri
- Run by
- Washington University School of Medicine
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Safety and Tolerability of Ziftomenib Combinations in Patients With Relapsed/Refractory Acute Myeloid Leukemia
The safety, tolerability, and antileukemic response of ziftomenib in combination with standard of care treatments for patients with relapsed/refractory acute myeloid leukemia will be examined with the following agents: FLAG-IDA, low-dose cytarabine, and gilteritinib.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Banner MD Anderson Cancer Center, Gilbert, Arizona
- Locations
- 45 in total
- Run by
- Kura Oncology, Inc.
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A Study of T-Cell Receptor Engineered Donor T Cells in Subjects Undergoing Allogeneic Peripheral Blood Stem Cell Transplantation
This is a multicenter, genetically-randomized, controlled, Phase 3 study evaluating the efficacy and safety of T-cell receptor-engineered donor T cells targeting HA-2 (TSC-101) administered following reduced-intensity conditioning (RIC) hematopoietic cell transplantation (HCT) in participants with …
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 26 in total
- Run by
- TScan Therapeutics, Inc.
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A Phase 1/3 Study of T-Cell Receptor Engineered Donor T Cells in Subjects Undergoing Allogeneic Peripheral Blood Stem Cell Transplantation
This is a multi-center, non-randomized, concurrent controlled, multi-arm, Phase 1 interventional, open-label, biologic assignment-based umbrella study evaluating the feasibility, safety and preliminary efficacy of an escalating dose regimen of up to 2 doses of TSC-100 and TSC-101 in patients with A…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 21 in total
- Run by
- TScan Therapeutics, Inc.
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A Study of CRD3874-SI in People With Leukemia
The purpose of this study is to find out whether CRD3874-SI is a safe treatment for participants with acute myeloid leukemia (AML).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering at Basking Ridge (All Protocol Activities), Basking Ridge, New Jersey
- Locations
- 7 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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Familial Investigations of Childhood Cancer Predisposition
NOTE: This is a research study and is not meant to be a substitute for clinical genetic testing. Families may never receive results from the study or may receive results many years from the time they enroll. If you are interested in clinical testing please consider seeing a local genetic counselor …
- Stage
- Not phased
- Ages
- Any age
- Site
- St. Jude Children's Research Hospital, Memphis, Tennessee
- Run by
- St. Jude Children's Research Hospital
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Pharmacokinetic Study of Venetoclax Tablets Crushed and Dissolved Into a Solution
The use of venetoclax-based therapies for pediatric patients with relapsed or refractory malignancies is increasingly common outside of the clinical trial setting. For patients who cannot swallow tablets, it is common to crush the tablets and dissolve them in liquid to create a solution. However, n…
- Stage
- Not phased
- Ages
- 0 to 38
- Site
- Children's Hospital Colorado, Aurora, Colorado
- Locations
- 5 in total
- Run by
- Children's Hospital Medical Center, Cincinnati
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Phase1b/2 Trial Of AZA + APG1252 In Patients With High-Risk AML
This is a phase Ib/II study that aims to investigate the safety, tolerability and explore the efficacy of BCL- XL inhibition in participants with high-risk AML.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UT MD Anderson, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
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A Randomized Study to Compare Post-transplant Cyclophosphamide, Sirolimus, Ruxolitinib and Post-transplant Cyclophosphamide, Sirolimus, Mycophenolate Mofetil to Prevent Graft Versus Host Disease
The goal of this clinical research study is to compare the effects of these drug combinations (cyclophosphamide, sirolimus, and MMF vs cyclophosphamide, sirolimus, and ruxolitinib) on the prevention of GVHD after a stem cell transplant.
- Stage
- Phase 2
- Ages
- 65 to 75
- Site
- The University of Texas M. D. Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
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Cardioprotection in AML
Patients with acute myeloid leukemia (AML) often receive a drug called daunorubicin. Daunorubicin is a type of drug called an anthracycline, which increases the risk of some damage to the heart. Beta blockers and angiotensin-converting enzyme inhibitors (ACEi) are two types of drugs that are often …
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of Virginia, Charlottesville, Virginia
- Run by
- University of Virginia
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MT2025-35 Allogeneic Hematopoietic Stem Cell Transplantation Using Reduced Intensity Conditioning Treosulfan and Fludarabine, With Post-Transplant Cytoxan (PTCy) for the Treatment of Hematological Diseases
This is a Phase II study following subjects proceeding with Treosulfan (36g/m2) preparative regimen followed by a related, unrelated, or partially matched family donor stem cell infusion, with post-transplant cyclophosphamide (PTCy) at 40mg/kg, tacrolimus and MMF for GVHD prophylaxis.
- Stage
- Phase 2
- Ages
- 2 to 75
- Site
- Masonic Cancer Center at University of Minnesota, Minneapolis, Minnesota
- Run by
- Masonic Cancer Center, University of Minnesota
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UAB 2419-CD34 Selection Using the Automated CliniMACS Prodigy
Patients with graft failure or delayed engraftment may benefit from a hematopoietic stem cell boost or an additional hematopoietic stem cell transplantation procedure. In such settings standard immune suppression strategies are avoided due to their myelosuppressive nature. Therefore those patients …
- Stage
- Phase 1
- Ages
- 0 to 75
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Run by
- University of Alabama at Birmingham
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MT2021-08T Cell Receptor Alpha/Beta Depletion PBSC Transplantation for Heme Malignancies
This is a phase II, open-label, prospective study of T cell receptor alpha/beta depletion (TCR α/β TCD) peripheral blood stem cell (PBSC) transplantation for children and adults with hematological malignancies. This is a safety/feasibility study of the investigational procedure/product.
- Stage
- Phase 2
- Ages
- Up to 60
- Site
- University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota
- Run by
- Masonic Cancer Center, University of Minnesota
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Revumenib in Combination With 7+3 + Midostaurin in AML
This research is being conducted to determine a safe and effective dose of revumenib that can be given in combination with standard induction (initial therapy to induce a remission) + FLT3 targeted therapy (midostaurin) and a single cycle of post-remission therapy + FLT3 targeted therapy (midostaur…
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Yale Cancer Center, New Haven, Connecticut
- Locations
- 2 in total
- Run by
- Richard Stone, MD
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Cord Blood Transplant in Children and Young Adults With Blood Cancers and Non-malignant Disorders
This is a single-arm study to investigate 1-year treatment related mortality (TRM) in patients with life threatening non-malignant and malignant hematologic disorders who do not have a matched related donor for allogeneic transplantation.
- Stage
- Phase 2
- Ages
- Up to 21
- Site
- Memorial Sloan Kettering Cancer Center, New York, New York
- Run by
- Memorial Sloan Kettering Cancer Center
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CC-486 and Venetoclax for Acute Myeloid Leukemia
This is an open label, dose escalation Phase I single institution pilot study for relapsed and refractory AML patients using CC-486 (oral azacitidine) with venetoclax. At the completion of dose escalation and after establishment of the MTD or recommended dose of CC-486 with venetoclax, an expansion…
- Stage
- Phase 1
- Ages
- 18 to 100
- Site
- CU Anschutz Medical Campus, Aurora, Colorado
- Locations
- 2 in total
- Run by
- University of Colorado, Denver
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A Long Term Follow-up Study of TScan TCR-T Products
The purpose of this Long-Term Follow-Up (LTFU) study is to monitor participants who have previously received TSC-100 or TSC-101 TCR-T therapies in the TSCAN-001 study. Participants will be monitored for 15 years from the date of TCR-T cell therapy administration to assess long-term safety and effic…
- Stage
- Not phased
- Ages
- 18 to 110
- Site
- City of Hope, Duarte, California
- Locations
- 2 in total
- Run by
- TScan Therapeutics, 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.