| Project Number | pCODR 10042 |
|---|---|
| Brand Name | Yervoy |
| Generic Name | Ipilimumab |
| Strength | 5mg/mL |
| Tumour Type | Skin and Melanoma |
| Indication | First Line Advanced Melanoma |
| Funding Request | For the first-line treatment of adult patients with advanced (unresectable or metastatic) melanoma |
| Review Status | Notification to Implement Issued |
| Pre Noc Submission | Yes |
| NOC Date | September 10, 2014 |
| Manufacturer | Bristol-Myers Squibb Canada |
| Sponsor | Bristol-Myers Squibb Canada |
| Submission Date | August 15, 2014 |
| Submission Deemed Complete | August 22, 2014 |
| Submission Type | New Indication |
| Prioritization Requested | Not Requested |
| Stakeholder Input Deadline ‡ | August 29, 2014 |
| Check-point meeting | October 6, 2014 |
| pERC Meeting | November 20, 2014 |
| Initial Recommendation Issued | December 4, 2014 |
| Feedback Deadline ‡ | December 18, 2014 |
| Final Recommendation Issued | December 22, 2014 |
| Notification to Implement Issued | January 14, 2015 |
‡ 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.
