dupilumab

Details

Key Milestones2
Call for patient/clinician input open28-Feb-23
Call for patient/clinician input closed24-Apr-23
Clarification:

- Patient input submission received from the Canadian Skin Patient Alliance (CSPA) & Eczéma Québec and Eczema Society of Canada

Submission received29-Mar-23
Submission accepted13-Apr-23
Review initiated14-Apr-23
Draft CADTH review report(s) provided to sponsor for comment06-Jul-23
Deadline for sponsors comments17-Jul-23
CADTH review report(s) and responses to comments provided to sponsor11-Aug-23
Expert committee meeting (initial)23-Aug-23
Draft recommendation issued to sponsor06-Sep-23
Draft recommendation posted for stakeholder feedback14-Sep-23
End of feedback period28-Sep-23
Final recommendation issued to sponsor and drug plans13-Oct-23
Final recommendation posted31-Oct-23
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)27-Oct-23
CADTH review report(s) posted12-Dec-23

axicabtagene ciloleucel

Details

Key Milestones2
Call for patient/clinician input open14-Feb-23
Call for patient/clinician input closed11-Apr-23
Clarification:

- Patient input submission received from Lymphoma Canada

Submission received13-Apr-23
Submission accepted27-Apr-23
Review initiated01-May-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment19-Jul-23
Deadline for sponsors comments28-Jul-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor31-Aug-23
Expert committee meeting (initial)13-Sep-23
Draft recommendation issued to sponsor26-Sep-23
Draft recommendation posted for stakeholder feedback05-Oct-23
End of feedback period20-Oct-23
Final recommendation issued to sponsor and drug plans02-Nov-23
Final recommendation posted21-Nov-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)17-Nov-23
Canada's Drug Agency review report(s) posted22-Jan-24

mirikizumab

Details

Key Milestones2
Call for patient/clinician input openFebruary 08, 2023
Call for patient/clinician input closedApril 03, 2023
Clarification:

- Patient input submission received from the Gastrointestinal Society

Submission receivedMarch 07, 2023
Submission acceptedMarch 22, 2023
Review initiatedMarch 23, 2023
Draft Canada's Drug Agency review report(s) provided to sponsor for commentJune 08, 2023
Deadline for sponsors commentsJune 19, 2023
Canada's Drug Agency review report(s) and responses to comments provided to sponsorJuly 14, 2023
Expert committee meeting (initial)July 26, 2023
Draft recommendation issued to sponsorAugust 09, 2023
Draft recommendation posted for stakeholder feedbackAugust 17, 2023
End of feedback periodAugust 31, 2023
Clarification:

- Reconsideration: minor revisions requested by sponsor

- Request for reconsideration accepted

Final recommendation issued to sponsor and drug plansNovember 16, 2023
Final recommendation postedDecember 04, 2023
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)November 30, 2023
Canada's Drug Agency review report(s) postedFebruary 09, 2024

andexanet alfa

Details

Key Milestones2
Call for patient/clinician input open01-Feb-23
Call for patient/clinician input closed27-Mar-23
Clarification:

- Patient input submission received from VTE-COS Patient Partners (members of CanVECTOR)

Submission received02-Mar-23
Submission accepted16-Mar-23
Review initiated20-Mar-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment08-Jun-23
Deadline for sponsors comments19-Jun-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor14-Jul-23
Expert committee meeting (initial)26-Jul-23
Draft recommendation issued to sponsor09-Aug-23
Draft recommendation posted for stakeholder feedback17-Aug-23
End of feedback period31-Aug-23
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meeting22-Nov-23
Final recommendation issued to sponsor and drug plans05-Dec-23
Final recommendation posted21-Dec-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)19-Dec-23
Canada's Drug Agency review report(s) posted08-Mar-24

polatuzumab vedotin

Details

Key Milestones2
Call for patient/clinician input open31-Jan-23
Call for patient/clinician input closed27-Mar-23
Clarification:

- Patient input submission received from Lymphoma Canada

Submission received01-Mar-23
Submission accepted15-Mar-23
Review initiated16-Mar-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment02-Jun-23
Deadline for sponsors comments13-Jun-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor27-Jul-23
Expert committee meeting (initial)09-Aug-23
Draft recommendation issued to sponsor22-Aug-23
Draft recommendation posted for stakeholder feedback31-Aug-23
End of feedback period15-Sep-23
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meeting06-Dec-23
Final recommendation posted15-Jan-24
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)11-Jan-24
Canada's Drug Agency review report(s) posted27-Feb-24

nelarabine

Details

Key Milestones2
Call for patient/clinician input open30-Jan-23
Call for patient/clinician input closed27-Mar-23
Clarification:

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

Submission received06-Mar-23
Submission accepted21-Mar-23
Review initiated22-Mar-23
Draft Canada's Drug Agency review report(s) provided to sponsor for comment21-Jun-23
Deadline for sponsors comments30-Jun-23
Canada's Drug Agency review report(s) and responses to comments provided to sponsor27-Jul-23
Expert committee meeting (initial)09-Aug-23
Draft recommendation issued to sponsor23-Aug-23
Draft recommendation posted for stakeholder feedback31-Aug-23
End of feedback period15-Sep-23
Final recommendation issued to sponsor and drug plans29-Sep-23
Final recommendation posted19-Oct-23
Deadline for sponsor to submit redaction requests on draft Canada's Drug Agency review report(s)17-Oct-23
Canada's Drug Agency review report(s) posted24-Nov-23

CADTH Pharmaceutical Reviews Update — Issue 34

CADTH Pharmaceutical Reviews Update — Issue 33