CDA | Evidence Driven
CDA | Evidence Driven

Mepolizumab

Details

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Generic Name:
Mepolizumab
Project Status:
Complete
Therapeutic Area:
Eosinophilic Granulomatosis with Polyangiitis
Call for patient/clinician input open:
Brand Name:
N/A
Project Line:
Reimbursement Review
Project Number:
SX0839-000
Call for patient/clinician input closed:
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
N/A
Submission Type:
Non-sponsored Submission
Fee Schedule:
Pending
Indications:
​Eosinophilic Granulomatosis with Polyangiitis (EGPA)
  1. 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.
Key Milestones2
Submission receivedDecember 19, 2023
Review initiatedDecember 20, 2023
Expert committee meeting (initial)July 04, 2024
Draft recommendation posted for stakeholder feedbackAugust 01, 2024
End of feedback periodAugust 16, 2024
Clarification:

- Reconsideration: minor revisions requested by drug programs

- Request for reconsideration accepted

Final recommendation posted-
CADTH review report(s) postedSeptember 10, 2024

Files

Draft Recommendation and Reasons View PDF
Proposed Project Scope View PDF
Clinical and Pharmacoeconomic Combined Report View PDF
Stakeholder Input View PDF

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Last Updated : October 30, 2024