AML Clinical Trials in Houston, Texas
8 studies are recruiting for aml in Houston, Texas 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.
Search these by distance from you
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
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 5 in total
- Run by
- CERo Therapeutics Holdings, Inc.
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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
- MD Anderson Cancer Center, Houston, Texas
- 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
- The University of Texas - MD Anderson Cancer Center, Houston, Texas
- 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
- MD Anderson, Houston, Texas
- Locations
- 21 in total
- Run by
- TScan Therapeutics, Inc.
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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
- Texas Children's Hospital, Houston, Texas
- 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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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
- Texas Children's Hospital/Baylor College of Medicine, Houston, Texas
- 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.