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.
Peter MacCallum Cancer Centre, Parkville, Victoria, Australia
Sir Charles Gairdener, Nedlands, Western Australia, Australia
Beth Israel Deaconness Medical, Boston, Massachusetts, United States
Dana Farber Cancer Institute, Boston, Massachusetts, United States
Mayo Clinic in Rochester, Rochester, Minnesota, United States
M D Anderson Cancer Center, Houston, Texas, United States
M D Anderson Cancer Center, Houston, Texas, United States
M D Anderson Cancer Center, Houston, Texas, United States
Alliance for Multispecialty Research (AMR) - Kansas City /ID# 242144, Kansas City, Missouri, United States
Northwell Health - Monter Cancer Center /ID# 245435, Lake Success, New York, United States
Icahn School of Medicine at Mount Sinai /ID# 242123, New York, New York, United States
Eisenhower Army Medical Center, Rancho Mirage, California, United States
Alta Bates Summit Medical Center, Berkeley, California, United States
Baylor Scott & White Health, Round Rock, Texas, United States
Covance Dallas, Dallas, Texas, United States
QPS Bio-Kinetic Clinical Applications, Springfield, Missouri, United States
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