FDA approves ruxolitinib extended-release tablets for MF, PV, and GVHD
The US Food and Drug Administration (FDA) has approved ruxolitinib (Jakafi XR) extended-release tablets for adults with intermediate or high-risk myelofibrosis and adults
The US Food and Drug Administration (FDA) has approved ruxolitinib (Jakafi XR) extended-release tablets for adults with intermediate or high-risk myelofibrosis and adults
In its second year, the Society of Hematologic Oncology (SOHO) will host its virtual SOHO Breakthroughs in Blood Cancers (SBBC) meeting, chaired by
Dr. Luke Fletcher leads a discussion at 11:30 am CST on May 15, 2026, on exploration of barriers and solutions for activating and
The National Medical Products Administration (NMPA) of China accepted the investigational New Drug application for the immunotherapy 6MW5311, a LILRB4/CD3 T-cell engager bispecific
The phase 3 trial evaluated the safety and efficacy of odronextamab, a CD20xCD3 bispecific antibody, in combination with CHOP chemotherapy for patients with
The phase 3 inMIND trial evaluated the efficacy and safety of tafasitamab in combination with rituximab and lenalidomide in adult patients with relapsed
Accord BioPharma, the therapy's manufacturer, expects a permanent Q-code from the US Centers for Medicare & Medicaid Services.
As we approach the end of the first quarter of 2026, I am pleased to share a brief update on the exceptional successes
In this video interview from SOHO Asia 2026, Dr. Feng-Ming Tien discusses the critical link between the immune microenvironment and therapeutic success in
The clearance allows the expansion of an international, phase 3 trial (CT103AC004) into Japan. This multi-center study evaluates the efficacy and safety of