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.
The University of Arizona Cancer Center, Tucson, Arizona, United States
City of Hope National Medical Center, Duarte, California, United States
Mayo Clinic in Florida, Jacksonville, Florida, United States
Hunan Cancer Hospital, Changsha, Hunan, China
Hospital de Clinicas de Porto Alegre, Porto Alegre, Rio Grande Do Sul, Brazil
Centro Gaucho Integrado - Mae de Deus Center, Porto Alegre, Rio Grande Do Sul, Brazil
The James Cancer Hospital, Columbus, Ohio, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Houston Methodist Hospital, Houston, Texas, United States
Mercy Health-Paducah Medical Oncology and Hematology, Paducah, Kentucky, United States
Greenebaum Comprehensive Cancer Center, Baltimore, Maryland, United States
Seattle Cancer Care Alliance, Seattle, Washington, United States
University of Pennsylvania Hospital, Philadelphia, Pennsylvania, United States
Ohio State University Hospital, Columbus, Ohio, United States
Cleveland Clinic Foundation, Cleveland, Ohio, United States
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