Non-radiographic axial spondyloarthritis

The PBS subsidises biological medicines for patients with non-radiographic axial spondyloarthritis.

Patient eligibility

The Pharmaceutical Benefits Scheme (PBS) subsidises treatment with biological medicines under the National Health Act 1953, section 85 for patients with non-radiographic axial spondyloarthritis.

Where the term biological medicine appears, it refers to bimekizumab, certolizumab pegol, golimumab, secukinumab and upadacitinib.

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 biological medicines.

Treatment specifics

To be eligible for PBS-subsidised treatment with biological medicines, patients must be treated by either a:

  • rheumatologist
  • clinical immunologist with expertise in the management of non-radiographic axial spondyloarthritis.

Authority applications

Applying for initial treatment

Apply for initial authority approval to prescribe PBS-subsidised biological medicines to treat non-radiographic axial spondyloarthritis in writing and either:

All written applications must include:

Applying for initial grandfather treatment

For patients who received non-PBS-subsidised bimekizumab treatment before 1 October 2024 for non-radiographic axial spondyloarthritis, apply for initial grandfather authority approval in writing and either:

All written applications must include:

Applying for continuing, change or recommencement of treatment

Applications to continue, change or recommence authority approval to prescribe PBS-subsidised biological medicines to treat non-radiographic axial spondyloarthritis can be made either:

More information

Call the PBS Complex Drugs Programs enquiry line for more information.

Page last updated: 2 October 2024.
QC 46841