FDA removes axi-cel limitations of use for primary CNS lymphoma
The US Food and Drug Administration (FDA) approved an update to the prescribing information for axicabtagene ciloleucel (Yescarta), removing the previous Limitations of
The US Food and Drug Administration (FDA) approved an update to the prescribing information for axicabtagene ciloleucel (Yescarta), removing the previous Limitations of
John DiPersio, MD, PhD, current president of SOHO and director of the Center for Gene and Cellular Immunotherapy at Washington University School of
The United States Food and Drug Administration (FDA) has signed off on a new, larger vial size for Nelarabine Injection for adult and
SOHO Israel is pleased to announce that the 4th Annual SOHO Israel Meeting, held in conjunction with the 10th International Davidoff Conference, will
In this video, the group discusses golcadomide's potential in relapsed or refractory follicular lymphoma, including combinations with rituximab in heavily pretreated patients, ongoing
The US Food and Drug Administration (FDA) granted approval for daratumumab and hyaluronidase-fihj (Darzalex Faspro, Janssen Biotech, Inc.) to be used in combination
The US Food and Drug Administration (FDA) has granted orphan drug designation to zavabresib (OPN-2853) for the treatment of myelofibrosis. The generic name
Dr. Hsin-An Hou, a professor at National Taiwan University Hospital, shares his excitement about the regional impact of the inaugural SOHO Asia meeting,
Sofi-cel, an allogeneic, off-the-shelf, CD7-targeted CAR-T cell therapy, has previously received regenerative medicine advanced therapy, fast track, orphan drug, and rare pediatric disease
The United States Food and Drug Administration cleared the Investigational New Drug application for KLN-1010, an in vivo BCMA-targeted CAR-T therapy, for patients