Post-Authorization Activity Table (PAAT) for Bosulif

The PAAT describes post-authorization activity for Bosulif, a product which contains the medicinal ingredient bosutinib. Based on Health Canada's review, the benefit/risk profile of Bosulif is favourable for the treatment of chronic, accelerated, or blast phase Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML) in adult patients with resistance or intolerance to prior tyrosine-kinase inhibitor (TKI) therapy, and for whom subsequent treatment with imatinib, nilotinib and dasatinib is not clinically appropriate. Read more here.