Last Updated : February 12, 2025
Details
FilesGeneric Name:
burosumab
Project Status:
Complete
Therapeutic Area:
Treatment of X-Linked Hypophosphatemia
Manufacturer:
Kyowa Kirin Canada, Inc.
Call for patient/clinician input open:
Brand Name:
Crysvita
Project Line:
Reimbursement Review
Project Number:
SR0818-000
Call for patient/clinician input closed:
NOC Status at Filing:
Post NOC
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
In addition to the criteria currently recommended by CADTH in the pediatric population of XLH patients (May 2020), the sponsor is requesting the following criteria for adult patients living with XLH: Initiation Criteria Aligned with international consensus guidelines, burosumab treatment can be initiated in adult patients, who have: a clinical presentation consistent with XLH, including: fasting hypophosphatemia, and normal renal function (defined as fasting serum creatinine below the age-adjusted upper limit of normal), and a confirmed PHEX gene variant in either the patient or in a directly related family member with appropriate X-linked inheritance and persistent bone and/or joint pain due to XLH, and/or osteomalacia that limits daily activities, and/or pseudofractures or osteomalacia-related fractures, and insufficient response or refractory to conventional therapy or if patients experience complications related to conventional therapy. Renewal Criteria Patients should be assessed on an annual basis for continued benefit. Treatment with burosumab can be renewed as long as the patient does not meet any of the discontinuation criteria. Discontinuation Criteria In adult patients burosumab should be discontinued if any of the following occur: hyperparathyroidism, nephrocalcinosis, evidence of fracture or pseudofracture based on radiographic assessment, or intolerable adverse events (e.g., one patient discontinued Study CL303 because of restless leg syndrome worsening from baseline).
Submission Type:
Reassessment
Fee Schedule:
Schedule A
Indications:
For the treatment of X-linked hypophosphataemia (XLH) in adult patients.
Recommendation Type:
Reimburse with clinical criteria and/or conditions
Final Recommendation:
- The requested reimbursement criteria are provided by the applicant and do not necessarily reflect the views of Canada's Drug Agency. Reimbursement criteria from Canada's Drug Agency will be documented in the final recommendation, if applicable.
Call for patient/clinician input open | November 14, 2023 |
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Call for patient/clinician input closed | January 12, 2024 |
Clarification: - Patient input submission received from Canadian XLH Network | |
Submission received | January 02, 2024 |
Submission accepted | January 16, 2024 |
Review initiated | January 17, 2024 |
Draft CADTH review report(s) provided to sponsor for comment | April 04, 2024 |
Deadline for sponsors comments | April 15, 2024 |
CADTH review report(s) and responses to comments provided to sponsor | May 09, 2024 |
Expert committee meeting (initial) | May 22, 2024 |
Draft recommendation issued to sponsor | June 04, 2024 |
Draft recommendation posted for stakeholder feedback | June 13, 2024 |
End of feedback period | June 27, 2024 |
Clarification: - Reconsideration: minor revisions requested by drug programs - Request for reconsideration accepted - Reconsideration: major revisions requested by drug programs - Request for reconsideration accepted | |
Expert committee meeting | September 25, 2024 |
Final recommendation issued to sponsor and drug plans | October 10, 2024 |
Final recommendation posted | October 29, 2024 |
Deadline for sponsor to submit redaction requests on draft CADTH review report(s) | October 25, 2024 |
CADTH review report(s) posted | February 12, 2025 |
Files
Last Updated : February 12, 2025