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RFA: Bosulif for Chronic Myeloid Leukemia – Details

Project Number pCODR RFA 0002
Brand Name Bosulif (RFA)
Generic Name Bosutinib
Tumour Type Leukemia
Indication Chronic Myeloid Leukemia
Request for Advice Question RFA Question from the Provincial Advisory Group: Is there evidence of clinical benefit sufficient to extend reimbursement eligibility of bosutinib “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 TKI therapy” without limiting it further to those “for whom subsequent treatment with imatinib, nilotinib and dasatinib is not clinically appropriate”?
Review Status Notification to Implement Issued
Manufacturer Pfizer Canada Inc.
Sponsor pCODR Provincial Advisory Group
Submission Date April 8, 2019
Submission Type Request for Advice
Stakeholder Input Deadline ‡ April 23, 2019
pERC Meeting July 18, 2019
pERC RFA Recommendation Issued August 1, 2019
Notification to Implement Issued August 2, 2019

‡ Only stakeholders (e.g., submitter/manufacturer(s) of the drug(s) in question, patient groups and registered clinician(s)) who contributed to the original submission in question are eligible to provide input on the Request for Advice Question. Deadlines for Input are by the end of the pCODR business day (5P.M. Eastern Time) of the date noted.