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|Project Number||pCODR 10214|
|Generic Name||Brentuximab Vedotin|
|Indication||Stage IV Hodgkin lymphoma (HL) in combination with doxorubicin, vinblastine, and dacarbazine (AVD)|
|Funding Request||For the treatment of previously untreated patients with Stage IV Hodgkin lymphoma (HL) in combination with doxorubicin, vinblastine, and dacarbazine (AVD).|
|Review Status||Notification to Implement Issued|
|Pre Noc Submission||No|
|NOC Date||May 2, 2019|
|Manufacturer||Seattle Genetics, Inc.|
|Sponsor||Seattle Genetics, Inc.|
|Submission Date||April 2, 2020|
|Submission Deemed Complete||April 21, 2020|
|Submission Type||New Indication|
|Stakeholder Input Deadline ‡||April 17, 2020|
|Check-point meeting||June 3, 2020|
|pERC Meeting||September 17, 2020|
|Initial Recommendation Issued||October 1, 2020|
|Feedback Deadline ‡||October 16, 2020|
|pERC Reconsideration Meeting||November 19, 2020|
|Final Recommendation Issued||December 3, 2020|
|Notification to Implement Issued||December 18, 2020|
‡ Patient Advocacy Groups (or individual patients and caregivers when there is no patient group) and Clinicians who are registered with pCODR are eligible to provide Input and Feedback. Deadlines for Input and Feedback are by the end of the pCODR business day (5P.M. Eastern Time) of the date noted.