Myelofibrosis

The PBS subsidises momelotinib and ruxolitinib for patients with myelofibrosis.

Note: This page has been decommissioned and is for information only.

Patient eligibility

The Pharmaceutical Benefits Scheme (PBS) subsidises treatment with momelotinib and ruxolitinib under the National Health Act 1953, section 85 for patients with myelofibrosis and classified as either:

  • high risk or intermediate-2 risk
  • intermediate-1 risk.

Patients must be eligible for the PBS and meet the relevant restriction criteria.

The Schedule of Pharmaceutical Benefits on the PBS website outlines the restrictions for prescribing ruxolitinib.

Authority applications

Applying for initial treatment

Applications for initial authority approval to prescribe PBS-subsidised momelotinib or ruxolitinib to treat myelofibrosis can be made either:

Applying for continuing treatment

Continuing PBS-subsidised treatment with momelotinib or ruxolitinib is Authority Required (Streamlined). You don’t need authority approval from us for the listed quantities and repeats.

More information

Call the PBS Authority line for more information.

Page last updated: 1 April 2025.
QC 33776