Childhood Cancer

You are here

Home » Grants » All grants tagged with "Acute Myeloid Leukemia (AML)"

All grants tagged with "Acute Myeloid Leukemia (AML)"

Development of allogeneic off-the-shelf gamma delta T cell product for pediatric AML
Norihiro Watanabe, PhD
Baylor College of Medicine
Innovation Grants, Awarded 2024
RAF Dimer Inhibitor Treatment in Pediatric Acute Myeloid Leukemia
Kevin Shannon, MD
The Regents of the University of California San Francisco
Innovation Grants, Awarded 2024
In vivo transdermal generation of CD33 CAR T-cells towards acute myeloid leukemia
Ruby Sims, PhD
University of California, Los Angeles
Young Investigator Grants, Awarded 2024
Cardiovascular comorbidities and cardiotoxicity as mechanisms for disparities in treatment outcomes for pediatric Acute Myeloid Leukemia
Emma Gombos
University of Pennsylvania
POST Program Grants, Awarded 2024
Acute myeloid leukemia; bloodstream infections and supportive care
Caleb Unterlack
Children’s Hospital of Philadelphia
POST Program Grants, Awarded 2024
Utilizing TIGIT-CAR natural killer cells to target acute myeloid leukemia
Kianna McEwen
Nationwide Children’s Hospital
POST Program Grants, Awarded 2024
Developing clinical guidance and improving care for AML-data abstraction
Nicolas Edgar
University of Utah
POST Program Grants, Awarded 2024
Therapeutic targeting of clonal hematopoiesis in RUNX1 mutant FPDMM
Robert Bowman, Ph.D.
University of Pennsylvania
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2024
Feasibility Study of Dual Inhibition of MDM2 and Tubulin in Treatment of AML
Muxiang Zhou, MD
Emory University
Reach Grants, Awarded 2023
Development of RADARS-based Therapy to Treat Fusion Molecule Driven Pediatric Malignancies
Alan B. Cantor, MD, PhD
Boston Children’s Hospital
Innovation Grants, Awarded 2023

Pages

All childhood cancer types

Featured Hero

Arianna Hines

Arianna is a firecracker. She is loving, empathetic, and bold. At a mere 13 months old, Arianna was diagnosed with neuroblastoma and began intensive treatment with some life-threatening complications. Today she is NED and her family raises money for ALSF.
Read more »