masitinib mesylate

Details

Key Milestones2
Call for patient/clinician input open29-Sep-22
Call for patient/clinician input closed18-Nov-22
Clarification:

- Patient input submission received from ALS Action Canada and ALS Society of Canada

Submission received28-Oct-22
Submission accepted15-Nov-22
Clarification:

- Submission was not accepted for review on 11 Nov 2022

Review initiated16-Nov-22
Clarification:

- Submission temporarily suspended

Draft CADTH review report(s) provided to sponsor for comment-
Deadline for sponsors comments-
CADTH review report(s) and responses to comments provided to sponsor-
Expert committee meeting (initial)-
Draft recommendation issued to sponsor-
Draft recommendation posted for stakeholder feedback-
End of feedback period-

ravulizumab

Details

Key Milestones2
Call for patient/clinician input open26-Sep-22
Call for patient/clinician input closed18-Nov-22
Clarification:

- Patient input submission received from Muscular Dystrophy Canada

Submission received25-Oct-22
Submission accepted08-Nov-22
Review initiated09-Nov-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment03-Feb-23
Deadline for sponsors comments14-Feb-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor09-Mar-23
Expert committee meeting (initial)22-Mar-23
Draft recommendation issued to sponsor04-Apr-23
Draft recommendation posted for stakeholder feedback13-Apr-23
End of feedback period27-Apr-23
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meeting26-Jul-23
Final recommendation issued to sponsor and drug plans08-Aug-23
Final recommendation posted24-Aug-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)22-Aug-23
Canada's Drug Agency review report(s) posted27-Oct-23

selumetinib

Details

Key Milestones2
Call for patient/clinician input openSeptember 26, 2022
Call for patient/clinician input closedNovember 18, 2022
Clarification:

- Patient input submission received from Canadian Organization for Rare Disorders (CORD)and Tumour Foundation of BC

Submission receivedOctober 28, 2022
Submission acceptedNovember 11, 2022
Review initiatedNovember 14, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentFebruary 03, 2023
Deadline for sponsors commentsFebruary 14, 2023
Canada's Drug Agency review report(s) and responses to comments provided to sponsorMarch 09, 2023
Expert committee meeting (initial)March 22, 2023
Draft recommendation issued to sponsorApril 05, 2023
Draft recommendation posted for stakeholder feedbackApril 13, 2023
End of feedback periodApril 27, 2023
Final recommendation issued to sponsor and drug plansMay 10, 2023
Final recommendation postedMay 29, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)May 25, 2023
Canada's Drug Agency review report(s) postedJuly 20, 2023

daprodustat

Details

Key Milestones2
Call for patient/clinician input openSeptember 26, 2022
Call for patient/clinician input closedNovember 18, 2022
Clarification:

- Patient input submission received from The Kidney Foundation of Canada

Submission receivedOctober 25, 2022
Submission acceptedNovember 08, 2022
Review initiatedNovember 09, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentFebruary 01, 2023
Deadline for sponsors commentsFebruary 10, 2023
Canada's Drug Agency review report(s) and responses to comments provided to sponsorMarch 09, 2023
Expert committee meeting (initial)March 22, 2023
Clarification:

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

- Voluntarily withdrawn by the sponsor on 24 Jul 2023.

palovarotene

Details

Key Milestones2
Call for patient/clinician input openSeptember 22, 2022
Call for patient/clinician input closedNovember 11, 2022
Clarification:

- Patient input submission received from The Canadian FOP Network (CFOPN) & The Canadian Organization for Rare Disorders (CORD)

Submission receivedOctober 21, 2022
Submission acceptedNovember 04, 2022
Review initiatedNovember 07, 2022
Draft Canada's Drug Agency review report(s) provided to sponsor for commentFebruary 06, 2023
Deadline for sponsors commentsFebruary 15, 2023
Canada's Drug Agency review report(s) and responses to comments provided to sponsorMarch 09, 2023
Expert committee meeting (initial)March 22, 2023
Draft recommendation issued to sponsorApril 05, 2023
Draft recommendation posted for stakeholder feedbackApril 13, 2023
End of feedback periodApril 27, 2023
Final recommendation issued to sponsor and drug plansMay 11, 2023
Final recommendation postedMay 30, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)May 26, 2023
Canada's Drug Agency review report(s) postedAugust 01, 2023

upadacitinib

Details

Key Milestones2
Call for patient/clinician input open16-Sep-22
Call for patient/clinician input closed11-Nov-22
Clarification:

- Patient input submission received from the Canadian Arthritis Patient Alliance, Canadian Spondylitis Association, Arthritis Society, CreakyJoints Canada

Submission received17-Oct-22
Submission accepted31-Oct-22
Review initiated01-Nov-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment02-Feb-23
Deadline for sponsors comments13-Feb-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor09-Mar-23
Expert committee meeting (initial)22-Mar-23
Draft recommendation issued to sponsor03-Apr-23
Draft recommendation posted for stakeholder feedback13-Apr-23
End of feedback period27-Apr-23
Final recommendation issued to sponsor and drug plans11-May-23
Final recommendation posted30-May-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)26-May-23
Canada's Drug Agency review report(s) posted28-Aug-23

vericiguat

Details

Key Milestones2
Call for patient/clinician input open15-Sep-22
Call for patient/clinician input closed04-Nov-22
Clarification:

- Patient input submission received from HeartLife Foundation and Heart function clinic Vancouver General Hospital, St Paul's Hospital

Submission received14-Oct-22
Submission accepted28-Oct-22
Review initiated31-Oct-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment19-Jan-23
Deadline for sponsors comments31-Jan-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor09-Mar-23
Expert committee meeting (initial)22-Mar-23
Draft recommendation issued to sponsor10-May-23
Draft recommendation posted for stakeholder feedback18-May-23
End of feedback period02-Jun-23
Final recommendation issued to sponsor and drug plans14-Jun-23
Final recommendation posted30-Jun-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)28-Jun-23
Canada's Drug Agency review report(s) posted30-Aug-23

CADTH Pharmaceutical Reviews Update — Issue 31

deucravacitinib

Details

Key Milestones2
Call for patient/clinician input open29-Aug-22
Call for patient/clinician input closed24-Oct-22
Clarification:

- Patient input submission received from the Canadian Psoriasis Network (CPN) and Canadian Association of Psoriasis Patients (CAPP)

Submission received27-Sep-22
Submission accepted12-Oct-22
Review initiated13-Oct-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment03-Jan-23
Deadline for sponsors comments12-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 sponsor07-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 meeting26-Jul-23
Final recommendation issued to sponsor and drug plans
Final recommendation posted24-Aug-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)22-Aug-23
Canada's Drug Agency review report(s) posted25-Oct-23

ciltacabtagene autoleucel

Details

Key Milestones2
Call for patient/clinician input open25-Aug-22
Call for patient/clinician input closed17-Oct-22
Clarification:

- Patient input submission received from Myeloma Canada

Submission received23-Sep-22
Submission accepted07-Oct-22
Review initiated11-Oct-22
Draft Canada's Drug Agency review report(s) provided to sponsor for comment22-Dec-22
Deadline for sponsors comments10-Jan-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor24-Feb-23
Expert committee meeting (initial)08-Mar-23
Draft recommendation issued to sponsor21-Mar-23
Draft recommendation posted for stakeholder feedback30-Mar-23
End of feedback period14-Apr-23
Final recommendation issued to sponsor and drug plans01-May-23
Final recommendation posted17-May-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)15-May-23
Canada's Drug Agency review report(s) posted02-Aug-23