NSCLC without actionable oncogenic alterations

lutetium vipivotide tetraxetan

Details

Key Milestones2
Call for patient/clinician input open22-Jun-22
Call for patient/clinician input closed22-Aug-22
Clarification:

- Patient input submission received from and the Canadian Cancer Society and the Canadian Cancer Survivor Network

Submission received21-Jul-22
Submission accepted24-Aug-22
Review initiated25-Aug-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment16-Nov-22
Deadline for sponsors comments25-Nov-22
Canada's Drug Agency review report(s) and responses to comments provided to sponsor22-Dec-22
Expert committee meeting (initial)11-Jan-23
Draft recommendation issued to sponsor24-Jan-23
Draft recommendation posted for stakeholder feedback02-Feb-23
End of feedback period16-Feb-23
Final recommendation issued to sponsor and drug plans03-Mar-23
Final recommendation posted22-Mar-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)20-Mar-23
Canada's Drug Agency review report(s) posted18-May-23

durvalumab

Details

Key Milestones2
Call for patient/clinician input openJune 14, 2022
Call for patient/clinician input closedAugust 08, 2022
Submission receivedJuly 14, 2022
Review initiatedJuly 29, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentOctober 21, 2022
Deadline for sponsors commentsNovember 01, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorNovember 29, 2022
Expert committee meeting (initial)December 07, 2022
Draft recommendation issued to sponsorDecember 20, 2022
Draft recommendation posted for stakeholder feedbackJanuary 05, 2023
End of feedback periodJanuary 19, 2023
Final recommendation issued to sponsor and drug plansFebruary 03, 2023
Final recommendation postedFebruary 22, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)February 17, 2023
Canada's Drug Agency review report(s) postedApril 27, 2023

belimumab

Details

Key Milestones2
Call for patient/clinician input openJune 08, 2022
Call for patient/clinician input closedJuly 29, 2022
Clarification:

- Patient input submission received from Canadian Arthritis Patient Alliance, Arthritis Society, Canadian Skin Patient Alliance, CreakyJoints, Arthritis Consumer Experts, The Kidney Foundation of Canada, Lupus Canada, and Lupis Ontario

Submission receivedJuly 07, 2022
Submission acceptedJuly 22, 2022
Review initiatedJuly 22, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentOctober 06, 2022
Deadline for sponsors commentsOctober 18, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorNovember 11, 2022
Expert committee meeting (initial)November 23, 2022
Draft recommendation issued to sponsorDecember 05, 2022
Draft recommendation posted for stakeholder feedbackDecember 15, 2022
End of feedback periodJanuary 06, 2023
Final recommendation issued to sponsor and drug plansJanuary 19, 2023
Final recommendation posted
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)February 03, 2023
Canada's Drug Agency review report(s) postedApril 10, 2023

abiraterone acetate and prednisolone

Details

Key Milestones2
Call for patient/clinician input open06-Jun-22
Call for patient/clinician input closed29-Jul-22
Clarification:

- Patient input submission received from the Canadian Cancer Society

Call for industry input open06-Jun-22
Call for industry input closed29-Jul-22
Review initiated06-Jun-22
Expert committee meeting (initial)29-Jun-23
Draft recommendation posted for stakeholder feedback20-Jul-23
End of feedback period03-Aug-23
Final recommendation posted08-Sep-23
Canada's Drug Agency review report(s) posted08-Sep-23

brolucizumab

Details

Key Milestones2
Call for patient/clinician input openJune 02, 2022
Call for patient/clinician input closedJuly 22, 2022
Clarification:

- Patient input submission received from Fighting Blindness Canada, The Canadian Council of the Blind, CNIB, Vision Loss Rehabilitation Canada, Diabetes Canada

Submission receivedJune 30, 2022
Submission acceptedJuly 15, 2022
Review initiatedJuly 18, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentOctober 06, 2022
Deadline for sponsors commentsOctober 18, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorNovember 11, 2022
Expert committee meeting (initial)November 23, 2022
Draft recommendation issued to sponsorDecember 07, 2022
Draft recommendation posted for stakeholder feedbackDecember 15, 2022
End of feedback periodJanuary 06, 2023
Final recommendation issued to sponsor and drug plansJanuary 18, 2023
Final recommendation postedFebruary 08, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)February 02, 2023
Canada's Drug Agency review report(s) postedMarch 29, 2023

dupilumab

Details

Key Milestones2
Call for patient/clinician input openMay 26, 2022
Call for patient/clinician input closedJuly 15, 2022
Clarification:

- Patient input submission received from Asthma Canada

Submission receivedJune 28, 2022
Submission acceptedJuly 13, 2022
Review initiatedJuly 14, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentOctober 05, 2022
Deadline for sponsors commentsOctober 17, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorNovember 11, 2022
Expert committee meeting (initial)November 23, 2022
Draft recommendation issued to sponsorDecember 07, 2022
Draft recommendation posted for stakeholder feedbackDecember 15, 2022
End of feedback periodJanuary 06, 2023
Final recommendation issued to sponsor and drug plansJanuary 20, 2023
Final recommendation postedFebruary 08, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)February 06, 2023
Canada's Drug Agency review report(s) postedApril 18, 2023

pembrolizumab

Details

Key Milestones2
Call for patient/clinician input openMay 20, 2022
Call for patient/clinician input closedJuly 15, 2022
Clarification:

- Patient input submission received from Canadian Breast Cancer Network and Rethink Breast Cancer

Submission receivedJune 20, 2022
Submission acceptedJuly 05, 2022
Review initiatedJuly 06, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentSeptember 20, 2022
Deadline for sponsors commentsSeptember 29, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorOctober 28, 2022
Expert committee meeting (initial)November 09, 2022
Draft recommendation issued to sponsorNovember 22, 2022
Draft recommendation posted for stakeholder feedbackDecember 01, 2022
End of feedback periodDecember 15, 2022
Final recommendation issued to sponsor and drug plansJanuary 06, 2023
Final recommendation postedJanuary 24, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)January 20, 2023
Canada's Drug Agency review report(s) postedMarch 20, 2023

darolutamide

Details

Key Milestones2
Call for patient/clinician input openMay 17, 2022
Call for patient/clinician input closedJuly 11, 2022
Clarification:

- Patient input submission received from Canadian Cancer Society and Canadian Cancer Survivor Network

Submission receivedJune 16, 2022
Submission acceptedJune 30, 2022
Review initiatedJuly 04, 2022
Draft CADTH review report(s) provided to sponsor for commentSeptember 26, 2022
Deadline for sponsors commentsOctober 05, 2022
CADTH review report(s) and responses to comments provided to sponsorOctober 28, 2022
Expert committee meeting (initial)November 09, 2022
Draft recommendation issued to sponsorNovember 23, 2022
Draft recommendation posted for stakeholder feedbackDecember 01, 2022
End of feedback periodDecember 15, 2022
Final recommendation issued to sponsor and drug plansJanuary 05, 2023
Final recommendation postedJanuary 23, 2023
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)January 19, 2023
CADTH review report(s) postedMarch 28, 2023

axicabtagene ciloleucel

Details

Key Milestones2
Call for patient/clinician input openMay 11, 2022
Call for patient/clinician input closedJuly 04, 2022
Clarification:

- Patient input submission received from Lymphoma Canada

Submission receivedJune 09, 2022
Submission acceptedJune 23, 2022
Review initiatedJune 24, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentSeptember 16, 2022
Deadline for sponsors commentsSeptember 27, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorOctober 28, 2022
Expert committee meeting (initial)November 09, 2022
Draft recommendation issued to sponsorDecember 20, 2022
Draft recommendation posted for stakeholder feedbackJanuary 05, 2023
End of feedback periodJanuary 19, 2023
Final recommendation postedFebruary 22, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)February 17, 2023
Canada's Drug Agency review report(s) postedJune 09, 2023