mavacamten

Details

Key Milestones2
Call for patient/clinician input openAugust 24, 2022
Call for patient/clinician input closedOctober 17, 2022
Clarification:

- Patient input submission received from the Canadian Heart Patient Alliance and the HeartLife Foundation

Submission receivedSeptember 22, 2022
Submission acceptedOctober 06, 2022
Review initiatedOctober 07, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentJanuary 05, 2023
Deadline for sponsors commentsJanuary 16, 2023
Canada's Drug Agency review report(s) and responses to comments provided to sponsorFebruary 09, 2023
Expert committee meeting (initial)February 22, 2023
Draft recommendation issued to sponsorMarch 08, 2023
Draft recommendation posted for stakeholder feedbackMarch 16, 2023
End of feedback periodMarch 31, 2023
Final recommendation issued to sponsor and drug plansApril 14, 2023
Final recommendation postedMay 03, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)May 01, 2023
Canada's Drug Agency review report(s) postedJune 23, 2023

nivolumab

Details

Key Milestones2
Call for patient/clinician input openAugust 15, 2022
Call for patient/clinician input closedOctober 07, 2022
Clarification:

- Patient input submission received from Canadian Cancer Society, Lung Cancer Canada

Submission receivedSeptember 13, 2022
Submission acceptedSeptember 27, 2022
Review initiatedSeptember 28, 2022
Draft CADTH review report(s) provided to sponsor for commentDecember 15, 2022
Deadline for sponsors commentsJanuary 03, 2023
CADTH review report(s) and responses to comments provided to sponsorJanuary 26, 2023
Expert committee meeting (initial)February 08, 2023
Draft recommendation issued to sponsorFebruary 22, 2023
Draft recommendation posted for stakeholder feedbackMarch 02, 2023
End of feedback periodMarch 16, 2023
Final recommendation issued to sponsor and drug plansMarch 30, 2023
Final recommendation postedApril 18, 2023
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)April 14, 2023
CADTH review report(s) postedJuly 11, 2023

brexucabtagene autoleucel

Details

Key Milestones2
Call for patient/clinician input open10-Aug-22
Call for patient/clinician input closed30-Sep-22
Clarification:

- Patient input submission received from The Leukemia & Lymphoma Society of Canada.

Submission received15-Sep-22
Submission accepted29-Sep-22
Review initiated03-Oct-22
Draft CADTH review report(s) provided to sponsor for comment19-Dec-22
Deadline for sponsors comments05-Jan-23
CADTH review report(s) and responses to comments provided to sponsor26-Jan-23
Expert committee meeting (initial)08-Feb-23
Draft recommendation issued to sponsor22-Feb-23
Draft recommendation posted for stakeholder feedback02-Mar-23
End of feedback period16-Mar-23
Final recommendation issued to sponsor and drug plans29-Mar-23
Final recommendation posted17-Apr-23
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)13-Apr-23
CADTH review report(s) posted09-Jun-23

ferumoxytol

Details

Key Milestones2
Call for patient/clinician input openAugust 03, 2022
Call for patient/clinician input closedSeptember 23, 2022
Clarification:

- Patient input submission received from the Gastrointestinal Society

Submission receivedAugust 31, 2022
Submission acceptedSeptember 15, 2022
Review initiatedSeptember 16, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentNovember 30, 2022
Deadline for sponsors commentsDecember 09, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorJanuary 13, 2023
Expert committee meeting (initial)January 25, 2023
Clarification:

- CDEC recommendation held pending receipt of NOC and evaluation of the finalized submission requirements.

- Withdrawn by the sponsor on 20 Mar 2023

difelikefalin

Details

Key Milestones2
Call for patient/clinician input open03-Aug-22
Call for patient/clinician input closed23-Sep-22
Clarification:

- Patient input submission received from The Kidney Foundation of Canada

Submission received22-Sep-22
Submission accepted06-Oct-22
Review initiated07-Oct-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment21-Dec-22
Deadline for sponsors comments09-Jan-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor09-Feb-23
Expert committee meeting (initial)22-Feb-23
Draft recommendation issued to sponsor06-Mar-23
Draft recommendation posted for stakeholder feedback16-Mar-23
End of feedback period31-Mar-23
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meeting28-Jun-23
Final recommendation issued to sponsor and drug plans13-Jul-23
Final recommendation posted31-Jul-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)01-Aug-23
Canada's Drug Agency review report(s) posted27-Sep-23

pegcetacoplan

Details

Key Milestones2
Call for patient/clinician input openJuly 28, 2022
Call for patient/clinician input closedSeptember 19, 2022
Clarification:

- Patient input submission received from the Canadian Association of PNH Patients & AAMAC

Submission receivedAugust 26, 2022
Submission acceptedSeptember 12, 2022
Review initiatedSeptember 13, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentNovember 29, 2022
Deadline for sponsors commentsDecember 08, 2022
Canada's Drug Agency review report(s) and responses to comments provided to sponsorJanuary 13, 2023
Expert committee meeting (initial)January 25, 2023
Draft recommendation issued to sponsorFebruary 09, 2023
Draft recommendation posted for stakeholder feedbackFebruary 16, 2023
End of feedback periodMarch 03, 2023
Final recommendation issued to sponsor and drug plansMarch 20, 2023
Final recommendation postedApril 05, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)April 03, 2023
Canada's Drug Agency review report(s) postedMay 18, 2023

dupilumab

Details

Key Milestones2
Request for Advice receivedJuly 15, 2022
Manufacturer informed of request for adviceJuly 25, 2022
Manufacturer information or comments dueAugust 09, 2022
Request for Advice initiatedAugust 10, 2022
Draft Canada's Drug Agency review report(s) sent to sponsorOctober 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
Expert committee meeting (initial)November 23, 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 06, 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) postedApril 13, 2023

sotorasib

Details

Key Milestones2
Call for patient/clinician input openJuly 21, 2022
Call for patient/clinician input closedSeptember 12, 2022
Clarification:

- Patient input submission received from Lung Cancer Canada, Lung Health Foundation, and Canadian Cancer Survivor Network.

Submission receivedAugust 19, 2022
Submission acceptedSeptember 02, 2022
Review initiatedSeptember 06, 2022
Draft CADTH review report(s) provided to sponsor for commentJuly 20, 2023
Clarification:

- Submission temporarily suspended

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

Deadline for sponsors commentsJuly 31, 2023
CADTH review report(s) and responses to comments provided to sponsorAugust 31, 2023
Expert committee meeting (initial)September 13, 2023
Draft recommendation issued to sponsorSeptember 27, 2023
Draft recommendation posted for stakeholder feedbackOctober 05, 2023
End of feedback periodOctober 20, 2023
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meetingFebruary 14, 2024
Final recommendation postedMarch 19, 2024
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)March 14, 2024
CADTH review report(s) postedJuly 23, 2024

crisantaspase recombinant

Details

Key Milestones2
Call for patient/clinician input open20-Jul-22
Call for patient/clinician input closed12-Sep-22
Clarification:

- Patient input submission received from The Leukemia & Lymphoma Society of Canada (LLSC).

Submission received18-Aug-22
Submission accepted01-Sep-22
Review initiated02-Sep-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment17-Nov-22
Deadline for sponsors comments28-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
Clarification:

- Reconsideration: major revisions requested by drug programs

- Reconsideration accepted

Expert committee meeting12-Apr-23
Final recommendation issued to sponsor and drug plans26-Apr-23
Final recommendation posted15-May-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)11-May-23
Canada's Drug Agency review report(s) posted12-Jul-23

rivaroxaban

Details

Key Milestones2
Call for patient/clinician input openJuly 14, 2022
Call for patient/clinician input closedSeptember 02, 2022
Clarification:

- No patient input submission received

Call for industry input openJuly 14, 2022
Call for industry input closedSeptember 02, 2022
Review initiatedOctober 12, 2022
Expert committee meeting (initial)August 24, 2023
Draft recommendation posted for stakeholder feedback-
End of feedback periodOctober 06, 2023
Final recommendation postedOctober 30, 2023
Canada's Drug Agency review report(s) postedSeptember 21, 2023