Tagraxofusp is a CD123-directed cytotoxin. It is a fusion protein composed of a human interleukin-3 (IL-3) that is genetically fused to the catalytic and translocation domains of truncated diphtheria toxin (DT) produced in Escherichia coli. Tagraxofusp received its first global approval by the FDA on December 21, 2018 as the first FDA-approved treatment for ...
Tagraxofusp is indicated for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN). In the US, it is approved for use in adults and pediatric patients over 2 years old. In Europe, it is only approved for use in adults.
Stanford University, Palo Alto, California, United States
City of Hope Medical Center, Duarte, California, United States
Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
Royal Perth Hospital, Perth, Western Australia, Australia
University of California, Los Angeles, Los Angeles, California, United States
Children's Hospital Los Angeles, Los Angeles, California, United States
Children's Hospital Orange County, Orange, California, United States
UCSF School of Medicine, San Francisco, California, United States
Danyelle Coley, Charlottesville, Virginia, United States
M D Anderson Cancer Center, Houston, Texas, United States
M D Anderson Cancer Center, Houston, Texas, United States
Aou Di Bologna - Policlinico S. Orsola-Malpighi - Uoc Ematologia, Bologna, Italy
Asst Papa Giovanni Xxiii - Ospedale Di Bergamo - Sc Ematologia, Bergamo, Italy
Asst Degli Spedali Civili Di Brescia - Uo Ematologia, Brescia, Italy
M D Anderson Cancer Center, Houston, Texas, United States
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