Generating novel antibodies targeting AML-associated antigen and developing therapeutics based on these antibodies
Developing of innovative strategies to overcome the limitations of bispecific antibodies and improve AML immunotherapy
Developing genome editing-based genomic approach to improve safety of AML therapies
Overcoming checkpoint inhibition as an approach to combinatorial therapy for AML
Developing rational strategies to improve AML therapy with gemtuzumab ozogamicin and other antibody-drug conjugates
Developing new approaches to radioimmunotherapy of AML
Improving adoptive cell therapy for AML with chimeric antigen receptor (CAR)-modified immune effector cells
Exploring the value of natural killer (NK)-cell based immunotherapy for AML
Using genome-scale CRISPR/Cas9 knockout screes to develop rational combination therapies that overcome AML cell resistance to antibody-based therapeutics