Adult Classical Hodgkin Lymphoma

Details

Review Type: Rapid

Provisional Funding Algorithm

Draft Report Posted : 19-sept-2024
Stakeholder Feedback Deadline: 26-sept-2024
Final Report Posted: 15-nov-2024
 

crovalimab

Details

Key Milestones2
Call for patient/clinician input openAugust 19, 2024
Call for patient/clinician input closedOctober 15, 2024
Submission receivedOctober 01, 2024
Submission acceptedOctober 16, 2024
Review initiatedOctober 17, 2024
Draft CADTH review report(s) provided to sponsor for commentJanuary 08, 2025
Deadline for sponsors commentsJanuary 17, 2025
CDA-AMC review report(s) and responses to comments provided to sponsorFebruary 13, 2025
Expert committee meeting (initial)February 26, 2025
Draft recommendation issued to sponsorJune 12, 2025
Draft recommendation posted for stakeholder feedbackJune 19, 2025
End of feedback periodJuly 04, 2025
Final recommendation issued to sponsor and drug plansJuly 21, 2025
Final recommendation posted-
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)August 05, 2025
CDA-AMC review report(s) posted-

daratumumab

Details

Key Milestones2
Call for patient/clinician input open19-Aug-24
Call for patient/clinician input closed15-Oct-24
Submission received01-Oct-24
Submission accepted16-Oct-24
Draft CADTH review report(s) provided to sponsor for comment17-Jan-25
Deadline for sponsors comments29-Jan-25
CDA-AMC review report(s) and responses to comments provided to sponsor28-Feb-25
Expert committee meeting (initial)12-Mar-25
Draft recommendation issued to sponsor25-Mar-25
Draft recommendation posted for stakeholder feedback03-Apr-25
End of feedback period17-Apr-25
Final recommendation issued to sponsor and drug plans02-May-25
Final recommendation posted21-May-25
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)16-May-25
CDA-AMC review report(s) posted-

pasireotide

Details

Key Milestones2
Call for patient/clinician input openAugust 19, 2024
Call for patient/clinician input closedOctober 15, 2024
Submission receivedOctober 02, 2024
Submission acceptedOctober 17, 2024
Review initiatedOctober 18, 2024
Draft CADTH review report(s) provided to sponsor for commentJanuary 09, 2025
Deadline for sponsors commentsJanuary 20, 2025
CDA-AMC review report(s) and responses to comments provided to sponsorFebruary 13, 2025
Expert committee meeting (initial)February 26, 2025
Draft recommendation issued to sponsorMarch 10, 2025
Draft recommendation posted for stakeholder feedbackMarch 20, 2025
End of feedback periodApril 03, 2025
Clarification:

- Reconsideration: minor revisions requested by sponsor

- Request for reconsideration partially accepted

Final recommendation issued to sponsor and drug plansJuly 08, 2025
Final recommendation postedJuly 24, 2025
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)July 22, 2025
CDA-AMC review report(s) posted-

trofinetide

Details

Key Milestones2
Call for patient/clinician input open16-Aug-24
Call for patient/clinician input closed15-Oct-24
Submission received29-Oct-24
Submission accepted13-Nov-24
Review initiated14-Nov-24
Draft CADTH review report(s) provided to sponsor for comment05-Feb-25
Deadline for sponsors comments14-Feb-25
CDA-AMC review report(s) and responses to comments provided to sponsor13-Mar-25
Expert committee meeting (initial)26-Mar-25
Draft recommendation issued to sponsor09-Apr-25
Draft recommendation posted for stakeholder feedback17-Apr-25
End of feedback period05-May-25
Clarification:

- Reconsideration: major revisions requested by sponsor

Expert committee meeting23-Jul-25

omaveloxolone

Details

Key Milestones2
Call for patient/clinician input openAugust 14, 2024
Call for patient/clinician input closedOctober 07, 2024
Submission receivedOctober 02, 2024
Submission acceptedOctober 17, 2024
Review initiatedOctober 18, 2024
Draft CADTH review report(s) provided to sponsor for commentJanuary 09, 2025
Deadline for sponsors commentsJanuary 20, 2025
CDA-AMC review report(s) and responses to comments provided to sponsorFebruary 13, 2025
Expert committee meeting (initial)February 26, 2025
Draft recommendation issued to sponsorMarch 18, 2025
Draft recommendation posted for stakeholder feedbackMarch 27, 2025
End of feedback periodApril 10, 2025
Clarification:

- Reconsideration: major and minor revisions requested by sponsor

Expert committee meetingJune 25, 2025
Final recommendation issued to sponsor and drug plansJuly 10, 2025
Final recommendation postedJuly 28, 2025
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)July 24, 2025
CDA-AMC review report(s) posted-

belantamab mafodotin, pomalidomide, dexamethasone

Details

Key Milestones2
Call for patient/clinician input open07-Aug-24
Call for patient/clinician input closed07-Nov-24
Submission received19-Dec-24
Submission accepted10-Jan-25
Review initiated13-Jan-25
Draft CADTH review report(s) provided to sponsor for comment16-Apr-25
Deadline for sponsors comments29-Apr-25
CDA-AMC review report(s) and responses to comments provided to sponsor30-May-25
Expert committee meeting (initial)11-Jun-25
Draft recommendation issued to sponsor-
Clarification:

pERC recommendation held pending receipt of NOC and evaluation of the finalized submission requirements

Draft recommendation posted for stakeholder feedback-
End of feedback period-