- Status Pre-assessment
- Type New application
- Pre-PASC consultation Open
- Pre-MSAC consultation -
- Outcome Pending
Application details
Applicant
Reason for application
Referral from the National Blood Authority.
Service or technology in this application
Concizumab is a humanised recombinant monoclonal antibody of the immunoglobulin G4 isotype for patients with haemophilia B. It is a once daily injection administered under the skin to help reduce the risk and/or severity of bleeding episodes experienced by people with haemophilia B.
Type: Therapeutic
Medical condition this application addresses
Haemophilia B (HMB) is a congenital lifelong bleeding disorder caused by deficiency or dysfunction of the coagulation protein factor IX (FIX). HMB patients experience spontaneous, painful bleeding episodes and prolonged, excessive haemorrhage following trauma or surgery.
Application documents
Application summary
PICO set
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Consultation survey and deadlines
The following consultation deadlines apply:
- Pre-PASC consultation deadline: Friday 11 July 2025 11:59pm AEDT
- Pre-MSAC consultation deadline:
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We welcome input from everyone. We are especially keen to hear from those with lived experience of the health condition, service or technology the applications are addressing.
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Meetings to consider this application
This application will be considered at the following meetings:
- PASC meeting: 15 August 2025
- ESC meeting:
- MSAC meeting:
Find out more about our meetings.
Outcome details
The outcome of this application is pending.
More information
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