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Nelarabine for Acute Lymphoblastic Leukemia - Details

Project Number pCODR 10170
Brand Name Atriance
Generic Name Nelarabine
Strength 650 mg
Tumour Type Leukemia
Indication Acute Lymphoblastic Leukemia
Funding Request Individuals, aged 1–30 years, newly diagnosed with intermediate- or high-risk (CNS1 or CNS 2) T-ALL, stages II-IV, during upfront therapy.
Review Status Pending
Pre Noc Submission No
NOC Date July 31, 2015
Manufacturer Novartis Pharmaceuticals Canada Inc.
Submitter Pediatric Oncology Group of Ontario
Submission Date (Target Date) June 14, 2019
Submission Type New Indication
Prioritization Requested
Stakeholder Input Deadline (target date based on target submission date) ‡ June 28, 2019
Check-point meeting (target date)
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.