Final remarks and presentation of awards.
FDA Grants Fast Track Designation to Novel FLT3/CD3 Bispecific in R/R AML
Phase 1 data related to CLN-049 for patients with acute myeloid leukemia will be presented at the 2025 ASH Annual Meeting and Exposition.
Evolutions Across NSCLC, Multiple Myeloma, and AML at Georgia Cancer Center
Experts from Georgia Cancer Center highlight ongoing retrospective studies, translational research, and other initiatives across different cancers.
Olutasidenib Maintains Durable Responses in IDH1+ AML for 5 Years
Among all patients with AML enrolled in the trial who received olutasidenib, the CR or CRh rate was 35%, with 55% of responders responding within 2 months.
Charting the Evolution of TKIs and Finding the Next Breakthrough in CML
Jorge Cortes, MD, outlines the impact of imatinib in chronic myeloid leukemia and highlights future initiatives in the field.
FDA Approves Ziftomenib in R/R NPM1-Mutated Acute Myeloid Leukemia
Clinical data from the phase 1b/2 KOMET-001 trial support the agency’s approval of ziftomenib in this patient population.
FDA Approves Abbreviated NDA for Dasatinib Tablets in Leukemia Indications
The newly approved dasatinib tablets are therapeutically equivalent and approved in the same indications as reference dasatinib.