ivosidenib

Details

Generic Name:
ivosidenib
Project Status:
Active
Therapeutic Area:
Acute myeloid leukemia (AML)
Manufacturer:
Servier Canada Inc
Call for patient/clinician input open:
Brand Name:
TBC
Project Line:
Reimbursement Review
Project Number:
PC0349-000
Call for patient/clinician input closed:
Tumour Type:
Leukemia
NOC Status at Filing:
Pre NOC
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
Ivosidenib in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) with an isocitrate dehydrogenase-1 (IDH1) R132 mutation who are not eligible to receive intensive induction chemotherapy.
Submission Type:
Initial
Companion Diagnostics:
Yes
Fee Schedule:
Schedule A
Indications:
​Ivosidenib in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) with an isocitrate dehydrogenase-1 (IDH1) R132 mutation who are not eligible to receive intensive induction chemotherapy.
  1. The requested reimbursement criteria are provided by the applicant and do not necessarily reflect the views of CADTH. Reimbursement criteria from CADTH will be documented in the final recommendation, if applicable.
Key Milestones2
Call for patient/clinician input openFebruary 05, 2024
Call for patient/clinician input closedApril 02, 2024
Clarification:

- Patient input submission received from The Leukemia and Lymphoma Society of Canada (LLSC) and Heal Canada

Submission receivedMarch 19, 2024
Submission acceptedApril 03, 2024
Review initiatedApril 04, 2024
Draft CADTH review report(s) provided to sponsor for commentJune 19, 2024
Deadline for sponsors commentsJune 28, 2024
CADTH review report(s) and responses to comments provided to sponsorAugust 01, 2024
Expert committee meeting (initial)August 14, 2024
Draft recommendation issued to sponsorAugust 26, 2024
To
August 28, 2024
Draft recommendation posted for stakeholder feedbackSeptember 05, 2024
End of feedback periodSeptember 19, 2024