avacopan

Details

Files
Generic Name:
avacopan
Project Status:
Complete
Therapeutic Area:
Antineutrophil cytoplasmic antibody-associated vasculitis
Manufacturer:
Otsuka Canada Pharmaceutical Inc.
Brand Name:
Tavneos
Project Line:
Reimbursement Review
Project Number:
SR0732-000
NOC Status at Filing:
Post NOC
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
For the adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (granulomatosis with polyangiitis [GPA] and microscopic polyangiitis [MPA]) in combination with standard background therapy including glucocorticoids. TAVNEOS does not eliminate glucocorticoid use.
Submission Type:
Initial
Fee Schedule:
Schedule A
Indications:
​For the adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (granulomatosis with polyangiitis [GPA] and microscopic polyangiitis [MPA]) in combination with standard background therapy including glucocorticoids. TAVNEOS does not eliminate glucocorticoid use.
Recommendation Type:
Do not reimburse
Final Recommendation:
  1. The requested reimbursement criteria are provided by the applicant and do not necessarily reflect the views of CADTH. Reimbursement criteria from CADTH will be documented in the final recommendation, if applicable.
Key Milestones2
Call for patient/clinician input openMarch 31, 2022
Call for patient/clinician input closedMay 20, 2022
Submission receivedOctober 14, 2022
Submission acceptedOctober 28, 2022
Review initiatedOctober 31, 2022
Draft CADTH review report(s) provided to sponsor for commentJanuary 26, 2023
Deadline for sponsors commentsFebruary 07, 2023
CADTH review report(s) and responses to comments provided to sponsorMarch 09, 2023
Expert committee meeting (initial)March 22, 2023
Draft recommendation issued to sponsorApril 04, 2023
Draft recommendation posted for stakeholder feedbackApril 13, 2023
End of feedback periodApril 27, 2023
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meetingJuly 26, 2023
Final recommendation postedAugust 28, 2023
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)August 24, 2023
CADTH review report(s) postedOctober 23, 2023