1805 – Concizumab for routine prophylaxis to prevent bleeding in patients with haemophilia B

Find out about the service or technology in this application and the medical condition it addresses. You can also view the application documents, the deadlines for providing consultation input and the outcome of the application when the MSAC process is complete.

  • Status Pre-assessment
  • Type New application
  • Pre-PASC consultation Open
  • Pre-MSAC consultation -
  • Outcome Pending

Application details

Applicant

Novo Nordisk Pharmaceuticals Pty. Limited

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. 

Consultation survey and deadlines

The following consultation deadlines apply:

  • Pre-PASC consultation deadline: Friday 11 July 2025 11:59pm AEDT
  • Pre-MSAC consultation deadline: 

For other ways to provide input, see how to have your say.

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.

Find out more about consultation.

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