| Project Number | pCODR 10199 |
|---|---|
| Brand Name | Adcetris |
| Generic Name | Brentuximab Vedotin |
| Strength | 50 mg / vial |
| Tumour Type | Lymphoma |
| Indication | Peripheral T-cell Lymphoma (PTCL) |
| Funding Request | For the treatment of previously untreated adult patients with systemic anaplastic large cell lymphoma (sALCL), peripheral T-cell lymphoma-not otherwise specified (PTCL-NOS) or angioimmunoblastic T-cell lymphoma (AITL), whose tumours express CD30, in combination with cyclophosphamide, doxorubicin, and prednisone (CHP). |
| Review Status | Under Review |
| Pre Noc Submission | Yes |
| NOC Date | November 22, 2019 |
| Manufacturer | Seattle Genetics, Inc. |
| Sponsor | Seattle Genetics, Inc. |
| Submission Date | October 8, 2019 |
| Submission Deemed Complete | October 23, 2019 |
| Submission Type | New Indication |
| Prioritization Requested | |
| Stakeholder Input Deadline ‡ | October 23, 2019 |
| Check-point meeting | January 7, 2020 |
| pERC Meeting (target date) | March 19, 2020 |
| Initial Recommendation Issued (target date) | |
| Feedback Deadline (target date) ‡ | |
| pERC Reconsideration Meeting (target date) | |
| Final Recommendation Issued (target date) | |
| Notification to Implement Issued |
‡ 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.
