danicopan

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Generic Name:
danicopan
Project Status:
Active
Therapeutic Area:
Paroxysmal nocturnal hemoglobinuria (PNH)
Manufacturer:
Alexion Pharma GmbH
Call for patient/clinician input open:
Brand Name:
Voydeya
Project Line:
Reimbursement Review
Project Number:
SR0815-000
Call for patient/clinician input closed:
NOC Status at Filing:
Pre NOC
Performance Metric:
Achieved
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
As an add-on to ravulizumab or eculizumab for the treatment of adult patients with paroxysmal nocturnal hemoglobinuria (PNH) who have residual hemolytic anemia due to extravascular hemolysis (EVH).
Submission Type:
Initial
Fee Schedule:
Schedule A
Indications:
As an add-on to ravulizumab or eculizumab for the treatment of adult patients with paroxysmal nocturnal hemoglobinuria (PNH) who have residual hemolytic anemia due to extravascular hemolysis (EVH).
  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
Call for patient/clinician input openFebruary 22, 2024
Call for patient/clinician input closedApril 15, 2024
Clarification:

- Patient input submission received from The Canadian Association of PNH Patients & Aplastic Anemia

Submission receivedApril 04, 2024
Submission acceptedApril 18, 2024
Review initiatedApril 19, 2024
Draft CADTH review report(s) provided to sponsor for commentJuly 11, 2024
Deadline for sponsors commentsJuly 22, 2024
CADTH review report(s) and responses to comments provided to sponsorAugust 16, 2024
Expert committee meeting (initial)August 28, 2024
Draft recommendation issued to sponsorSeptember 11, 2024
Draft recommendation posted for stakeholder feedbackSeptember 19, 2024
End of feedback periodOctober 04, 2024