epcoritamab

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Generic Name:
epcoritamab
Project Status:
Active
Therapeutic Area:
Relapsed or refractory diffuse large B-cell lymphoma
Manufacturer:
AbbVie Corporation
Call for patient/clinician input open:
Brand Name:
Epkinly
Project Line:
Reimbursement Review
Project Number:
PC0334-000
Call for patient/clinician input closed:
Tumour Type:
Lymphoma
NOC Status at Filing:
Post NOC
Biosimilar:
No
Manufacturer Requested Reimbursement Criteria1:
For the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma not otherwise specified (DLBCL NOS), DLBCL transformed from indolent lymphoma, high grade B-cell lymphoma (HGBCL), primary mediastinal B-cell lymphoma (PMBCL) or follicular lymphoma Grade 3B (FLG3b) after two or more lines of systemic therapy and who have previously received or are unable to receive CAR-T cell therapy.
Submission Type:
Initial
Fee Schedule:
Schedule A
Indications:
For the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma not otherwise specified (DLBCL NOS), DLBCL transformed from indolent lymphoma, high grade B-cell lymphoma (HGBCL), primary mediastinal B-cell lymphoma (PMBCL) or follicular lymphoma Grade 3B (FLG3b) after two or more lines of systemic therapy and who have previously received or are unable to receive CAR-T cell therapy.
Recommendation Type:
Time-limited reimbursement recommendation
Final Recommendation:
  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 open29-Sep-23
Call for patient/clinician input closed27-Nov-23
Clarification:

- Patient input submission received from Lymphoma Canada and the Leukemia & Lymphoma Society of Canada

Submission received14-Nov-23
Clarification:

Eligible for consideration as a time-limited recommendation

Submission accepted28-Nov-23
Review initiated29-Nov-23
Draft CADTH review report(s) provided to sponsor for comment23-Feb-24
Deadline for sponsors comments05-Mar-24
CADTH review report(s) and responses to comments provided to sponsor28-Mar-24
Expert committee meeting (initial)10-Apr-24
Draft recommendation issued to sponsor24-Apr-24
Draft recommendation posted for stakeholder feedback02-May-24
End of feedback period16-May-24
Final recommendation issued to sponsor and drug plans31-May-24
Final recommendation posted18-Jun-24
Deadline for sponsor to submit redaction requests on draft CADTH review report(s)14-Jun-24
CADTH review report(s) posted-