FDA panel votes 6-2 in favor of daratumumab for high-risk smoldering multiple myeloma
The US Food and Drug Administration (FDA)’s Oncologic Drugs Advisory Committee (ODAC) voted 6-2 that the results from the phase 3 AQUILA trial
The US Food and Drug Administration (FDA)’s Oncologic Drugs Advisory Committee (ODAC) voted 6-2 that the results from the phase 3 AQUILA trial
The third meeting of SOHO Israel and 9th International Davidoff conference, titled State of the Art and Next Questions, was held on May
A federal advisory panel voted 8-1 Tuesday that results from the global STARGLO trial, which was intended as the confirmatory trial for full
Saad Usmani, MD, of Memorial Sloan Kettering Cancer Center in New York, and Gwen Nichols, MD, CMO of the Leukemia & Lymphoma Society
Even in patients with myelodysplastic syndromes (MDS) who don’t have a mutation in tumor protein 53 (p53), the p53 protein might still be
In this video, James Wu, MD, a hematology/oncology fellow at the Medical College of Wisconsin, discusses a letter published in the journal Leukemia
Dr. Pui, co-leader of the hematological malignancies program at the St. Jude Children’s Research Hospital in Memphis, Tennessee, shares his gratitude for receiving
Three patients with chemotherapy-refractory Burkitt’s lymphoma achieved complete metabolic responses after treatment with glofitamab and polatuzumab vedotin, according to a recently published correspondence
ISB 2001, a trispecific T-cell engager targeting BCMA and CD38, showed expected immune activity and no dose-limiting toxicities in an ongoing phase 1
Investigators used RNA sequencing to create a new gene activity atlas that showed how normal blood cells developed. The technique also identified the