FDA to review sBLA for epcoritamab plus R2 in relapsed or refractory FL
The US Food and Drug Administration (FDA) will review a supplemental Biologics License Application (sBLA) for epcoritamab combined with rituximab and lenalidomide (R2)
The US Food and Drug Administration (FDA) will review a supplemental Biologics License Application (sBLA) for epcoritamab combined with rituximab and lenalidomide (R2)
Presession focused on MDS/MPN-related anemia. Participants can register for the presession and SOHO 2025 at soho.click/2025 . HOUSTON, April 3, 2025 /PRNewswire/ — The Society of Hematologic Oncology
An Italian real-world study assessed the use of asciminib in a compassionate use setting in heavily pretreated patients with chronic-phase chronic myeloid leukemia
The Center for Drug Evaluation (CDE) of the China National Medical Products Administration (NMPA) has granted Breakthrough Therapy Designation for mesutoclax for the
The US Food and Drug Administration (FDA) has granted Orphan Drug Designation for bexmarilimab for the treatment of patients with myelodysplastic syndromes (MDS).
A phase 1b/2 study found that the combination of azacitidine, venetoclax, and magrolimab was safe for the treatment of acute myeloid leukemia (AML),
Cord blood-derived natural killer (NK) cells pre-complexed with AFM13, a CD30/CD16A bispecific antibody, resulted in 2-year event-free and overall survival rates of 26.2%
A mouse model confirmed the aggressive nature of CD38 expression in multiple myeloma (MM), which induces widespread metastasis, extensive bone degradation, renal involvement,
A study presented at the American Association for Cancer Research Annual Meeting 2025 found that the investigational chimeric antigen receptor (CAR) therapy SENTI-202
The American Association for Cancer Research (AACR) has named Larry Saltzman, MD, a recipient of the 2025 Distinguished Public Service Award for his