| Project Number | pCODR 10155 |
|---|---|
| Brand Name | Tecentriq & Avastin |
| Generic Name | Atezolizumab & Bevacizumab |
| Strength | 1200 mg/20 mL (60 mg/mL) vial & 100 mg/4 mL (25 mg/mL) and 400mg/16mL (25 mg/mL) vials |
| Tumour Type | Lung |
| Indication | Non-Squamous Non-Small Cell Lung Cancer |
| Funding Request | For the treatment of metastatic EGFR and/or ALK positive non-squamous non-small cell lung cancer in patients who have progressed on treatment with targeted therapies. Maintenance TECENTRIQ should be continued until loss of clinical benefit or unacceptable toxicity. Maintenance AVASTIN should be continued until disease progression or unacceptable toxicity. |
| Review Status | Under Review |
| Pre Noc Submission | No |
| NOC Date | May 24, 2019 |
| Manufacturer | Hoffmann-La Roche Limited |
| Sponsor | Hoffmann-La Roche Limited |
| Submission Date | November 18, 2019 |
| Submission Deemed Complete | December 2, 2019 |
| Submission Type | New Indication |
| Prioritization Requested | |
| Stakeholder Input Deadline ‡ | December 2, 2019 |
| Check-point meeting (target date) | January 27, 2020 |
| pERC Meeting (target date) | |
| 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.
