pembrolizumab

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Generic Name:
pembrolizumab
Project Status:
Active
Therapeutic Area:
Advanced or metastatic malignant pleural mesothelioma
Manufacturer:
Merck Canada Inc.
Call for patient/clinician input open:
Brand Name:
Keytruda
Project Line:
Reimbursement Review
Project Number:
PC0387-000
Call for patient/clinician input closed:
Tumour Type:
Other
NOC Status at Filing:
Pre NOC
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
Keytruda in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of adult and pediatric (12 years and older) patients with unresectable advanced or metastatic malignant pleural mesothelioma (MPM).
Submission Type:
Initial
Fee Schedule:
Schedule A
Indications:
​Keytruda in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of adult and pediatric (12 years and older) patients with unresectable advanced or metastatic malignant pleural mesothelioma (MPM).
  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 openOctober 17, 2024
Call for patient/clinician input closedDecember 06, 2024
Submission receivedNovember 27, 2024
Submission acceptedDecember 11, 2024
Review initiatedDecember 12, 2024
Draft CADTH review report(s) provided to sponsor for commentMarch 24, 2025
Deadline for sponsors commentsApril 02, 2025
CADTH review report(s) and responses to comments provided to sponsorMay 02, 2025
Expert committee meeting (initial)May 14, 2025
Draft recommendation issued to sponsorMay 27, 2025
To
May 29, 2025
Draft recommendation posted for stakeholder feedbackJune 05, 2025
End of feedback periodJune 19, 2025