Pirtobrutinib is a small molecule and a highly selective non-covalent inhibitor of Bruton’s tyrosine kinase (BTK). Its high selectivity has been associated with lower discontinuation rates due to adverse events and a lower incidence of atrial fibrillation. Unlike BTK covalent inhibitors, such as ibrutinib, that bind to the cysteine 481 (Cys481) amino acid wi...
Pirtobrutinib is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two lines of systemic therapy, including a BTK inhibitor.
MedStar Georgetown University Hospital, Washington, District of Columbia, United States
Univ of Miami - Sylvester Comprehensive Cancer Center, Miami, Florida, United States
Moffitt Cancer Center, Tampa, Florida, United States
Stanford Cancer Center, Stanford, California, United States
MD Anderson Cancer Center, Houston, Texas, United States
Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States
Huntsman Cancer Institute at University of Utah, Salt Lake City, Utah, United States
Brigham & Women's Hospital, Boston, Massachusetts, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
MD Anderson Cancer Center, Houston, Texas, United States
Labcorp Drug Development, Dallas, Texas, United States
University of California, San Francisco, San Francisco, California, United States
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