CPX-351 is a dual-drug liposomal formulation of cytarabine and daunorubicin, approved by the FDA for the treatment of adults with newly diagnosed acute myeloid leukemia (AML) with myelodysplasia-related changes (AML-MRC) and therapy-related AML. Thomas Cluzeau, MD, PhD, Central University Hospital of Nice, Nice, France, discusses the latest news on CPX-351, including real-world experiences and trials in myelodysplastic syndrome (MDS). This interview took place at during 63rd ASH Annual Meeting and Exposition congress in Atlanta, GA.