bimekizumab

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Generic Name:
bimekizumab
Project Status:
Active
Therapeutic Area:
Psoriatic arthritis
Manufacturer:
UCB Canada Inc.
Call for patient/clinician input open:
Brand Name:
Bimzelx
Project Line:
Reimbursement Review
Project Number:
SR0803-000
Call for patient/clinician input closed:
NOC Status at Filing:
Pre NOC
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
The treatment of adult patients with active psoriatic arthritis. Bimzelx can be used alone or in combination with a conventional non-biologic disease-modifying antirheumatic drug (cDMARD) (e.g., methotrexate).
Submission Type:
Initial
Fee Schedule:
Schedule A
Indications:
​The treatment of adult patients with active psoriatic arthritis. Bimzelx can be used alone or in combination with a conventional non-biologic disease-modifying antirheumatic drug (cDMARD) (e.g., methotrexate).
  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 openAugust 23, 2023
Call for patient/clinician input closedOctober 17, 2023
Clarification:

- Patient input submission received from the ACE, CPN, ASC, CAPA, CAPP, CSA, and CJ

Submission receivedOctober 05, 2023
Submission acceptedOctober 20, 2023
Review initiatedOctober 23, 2023
Draft CADTH review report(s) provided to sponsor for commentJanuary 18, 2024
Deadline for sponsors commentsJanuary 30, 2024
CADTH review report(s) and responses to comments provided to sponsorMarch 14, 2024
Expert committee meeting (initial)March 27, 2024
Draft recommendation issued to sponsorApril 10, 2024
Draft recommendation posted for stakeholder feedbackApril 18, 2024
End of feedback periodMay 03, 2024