bimekizumab

Details

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 Canada's Drug Agency review report(s) provided to sponsor for commentJanuary 18, 2024
Deadline for sponsors commentsJanuary 30, 2024
Canada's Drug Agency 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
Final recommendation issued to sponsor and drug plansMay 15, 2024
Final recommendation postedJune 03, 2024
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)May 30, 2024
Canada's Drug Agency review report(s) postedSeptember 19, 2024

etranacogene dezaparvovec

Details

Key Milestones2
Call for patient/clinician input open22-Aug-23
Call for patient/clinician input closed17-Oct-23
Clarification:

- Patient input submission received from the Canadian Hemophilia Society

Submission received04-Oct-23
Submission accepted19-Oct-23
Review initiated20-Oct-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment11-Jan-24
Deadline for sponsors comments22-Jan-24
Canada's Drug Agency review report(s) and responses to comments provided to sponsor15-Feb-24
Expert committee meeting (initial)28-Feb-24
Draft recommendation issued to sponsor11-Mar-24
Draft recommendation posted for stakeholder feedback21-Mar-24
End of feedback period08-Apr-24
Final recommendation issued to sponsor and drug plans19-Apr-24
Final recommendation posted08-May-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)06-May-24
Canada's Drug Agency review report(s) posted26-Sep-24

infliximab

Details

Key Milestones2
Call for patient/clinician input open22-Aug-23
Call for patient/clinician input closed17-Oct-23
Clarification:

- Patient input submission received from the Gastrointestinal Society

Submission received04-Oct-23
Submission accepted19-Oct-23
Review initiated20-Oct-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment11-Jan-24
Deadline for sponsors comments22-Jan-24
Canada's Drug Agency review report(s) and responses to comments provided to sponsor15-Feb-24
Expert committee meeting (initial)28-Feb-24
Draft recommendation issued to sponsor11-Mar-24
Draft recommendation posted for stakeholder feedback21-Mar-24
End of feedback period08-Apr-24
Final recommendation issued to sponsor and drug plans22-Apr-24
Final recommendation posted09-May-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)07-May-24
Canada's Drug Agency review report(s) posted28-Aug-24

cannabidiol

Details

Key Milestones2
Call for patient/clinician input open18-Aug-23
Call for patient/clinician input closed17-Oct-23
Clarification:

- Patient input submission received from the Canadian Epilepsy Alliance

Submission received29-Sep-23
Submission accepted17-Oct-23
Review initiated18-Oct-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment09-Jan-24
Deadline for sponsors comments18-Jan-24
Canada's Drug Agency review report(s) and responses to comments provided to sponsor15-Feb-24
Expert committee meeting (initial)28-Feb-24
Draft recommendation issued to sponsor12-Mar-24
Draft recommendation posted for stakeholder feedback21-Mar-24
End of feedback period08-Apr-24
Final recommendation issued to sponsor and drug plans18-Apr-24
Final recommendation posted07-May-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)03-May-24
Canada's Drug Agency review report(s) posted23-Jul-24

osilodrostat

Details

Key Milestones2
Call for patient/clinician input openAugust 17, 2023
Call for patient/clinician input closedOctober 10, 2023
Clarification:

- Patient input submission received from Canadian Organization for Rare Disorders

Submission receivedOctober 16, 2023
Submission acceptedOctober 30, 2023
Clarification:

- Additional information has been received and the temporary suspension of the review has been lifted

Review initiatedOctober 31, 2023
Clarification:

- Submission temporarily suspended

Draft CADTH review report(s) provided to sponsor for commentOctober 10, 2025
Deadline for sponsors commentsOctober 22, 2025
CDA-AMC review report(s) and responses to comments provided to sponsorNovember 14, 2025
Expert committee meeting (initial)November 26, 2025
Draft recommendation issued to sponsorDecember 08, 2025
To
December 10, 2025
Draft recommendation posted for stakeholder feedbackDecember 18, 2025
End of feedback periodJanuary 09, 2026

cemiplimab

Details

Key Milestones2
Call for patient/clinician input openAugust 16, 2023
Call for patient/clinician input closedOctober 10, 2023
Clarification:

- Patient input submission received from Canadian Cancer Survivor Network, Lung Cancer Canada - Patient Group, and Lung Health Foundation / The Ontario Lung Association

Submission receivedSeptember 27, 2023
Submission acceptedOctober 13, 2023
Review initiatedOctober 16, 2023
Draft Canada's Drug Agency review report(s) provided to sponsor for commentJanuary 17, 2024
Deadline for sponsors commentsJanuary 29, 2024
Canada's Drug Agency review report(s) and responses to comments provided to sponsorMarch 01, 2024
Expert committee meeting (initial)March 13, 2024
Draft recommendation issued to sponsorMarch 26, 2024
Draft recommendation posted for stakeholder feedbackApril 04, 2024
End of feedback periodApril 18, 2024
Final recommendation issued to sponsor and drug plansMay 02, 2024
Final recommendation postedMay 21, 2024
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)May 16, 2024
Canada's Drug Agency review report(s) postedSeptember 18, 2024

cannabidiol

Details

Key Milestones2
Call for patient/clinician input open14-Aug-23
Call for patient/clinician input closed10-Oct-23
Clarification:

- Patient input submission received from the Canadian Epilepsy Alliance

Submission received25-Sep-23
Submission accepted11-Oct-23
Review initiated12-Oct-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment03-Jan-24
Deadline for sponsors comments12-Jan-24
Canada's Drug Agency review report(s) and responses to comments provided to sponsor15-Feb-24
Expert committee meeting (initial)28-Feb-24
Draft recommendation issued to sponsor12-Mar-24
Draft recommendation posted for stakeholder feedback21-Mar-24
End of feedback period08-Apr-24
Final recommendation issued to sponsor and drug plans18-Apr-24
Final recommendation posted07-May-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)03-May-24
Canada's Drug Agency review report(s) posted27-Jun-24

cannabidiol

Details

Key Milestones2
Call for patient/clinician input open10-Aug-23
Call for patient/clinician input closed29-Sep-23
Clarification:

-Patient input submission received from the Canadian Epilepsy Alliance

Submission received20-Sep-23
Submission accepted05-Oct-23
Review initiated06-Oct-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment21-Dec-23
Deadline for sponsors comments09-Jan-24
Canada's Drug Agency review report(s) and responses to comments provided to sponsor15-Feb-24
Expert committee meeting (initial)28-Feb-24
Draft recommendation issued to sponsor12-Mar-24
Draft recommendation posted for stakeholder feedback21-Mar-24
End of feedback period08-Apr-24
Final recommendation issued to sponsor and drug plans18-Apr-24
Final recommendation posted07-May-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)03-May-24
Canada's Drug Agency review report(s) posted14-Aug-24

nirmatrelvir/ritonavir

Details

Key Milestones2
Call for patient/clinician input open03-Aug-23
Call for patient/clinician input closed25-Sep-23
Clarification:

- Patient input submission received from the Gastrointestinal Society, Lung Health Foundation, Save Your Skin Foundation and Sickle Cell Awareness Group of Ontario

Submission received15-Sep-23
Submission accepted29-Sep-23
Review initiated03-Oct-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment07-Nov-23
Deadline for sponsors comments14-Nov-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor08-Dec-23
Expert committee meeting (initial)20-Dec-23
Draft recommendation issued to sponsor09-Jan-24
Draft recommendation posted for stakeholder feedback18-Jan-24
End of feedback period02-Feb-24
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meeting27-Mar-24
Final recommendation issued to sponsor and drug plans11-Apr-24
Final recommendation posted30-Apr-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)25-Apr-24
Canada's Drug Agency review report(s) posted09-Jul-24

fidanacogene elaparvovec

Details

Key Milestones2
Call for patient/clinician input openJune 20, 2023
Call for patient/clinician input closedAugust 14, 2023
Clarification:

- Patient input submission received from Canadian Hemophilia Society (CHS)

Submission receivedAugust 01, 2023
Submission acceptedAugust 16, 2023
Review initiatedAugust 17, 2023
Draft Canada's Drug Agency review report(s) provided to sponsor for commentNovember 02, 2023
Deadline for sponsors commentsNovember 14, 2023
Canada's Drug Agency review report(s) and responses to comments provided to sponsorDecember 08, 2023
Expert committee meeting (initial)December 20, 2023
Draft recommendation issued to sponsorJanuary 11, 2024
Draft recommendation posted for stakeholder feedbackJanuary 18, 2024
End of feedback periodFebruary 02, 2024
Final recommendation postedMarch 06, 2024
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)March 04, 2024
Canada's Drug Agency review report(s) postedJune 05, 2024