Psoriasis (PSOR) Program in Pharmaceutical Benefits Scheme (PBS) 012-18051130
This document outlines details of PBS-subsidised biological medicines for patients with psoriasis (PSOR).
PSOR and listing dates
PSOR is an autoimmune disease characterised by abnormally red, itchy and/or scaly patches of skin.
Listing dates:
- etanercept - 1 August 2006
- infliximab - 1 December 2007
- adalimumab - 1 June 2009
- ustekinumab - 1 March 2010
- etanercept (<18 years) - 1 August 2012
- secukinumab - 1 September 2015
- ixekizumab - 1 February 2017
- guselkumab - 1 February 2019
- tildrakizumab - 1 February 2019
- risankizumab (75 mg syringe) - 1 December 2019*
- ustekinumab (<18 years) - 1 October 2021
- bimekizumab - 1 October 2023
- risankizumab (150 mg pen) - 1 May 2024
* Note: risankizumab 75 mg syringe delisted 1 May 2024
See Written Authority Required Drugs for more details.
Treatment specifics
A break in treatment cycles is measured:
- from the date of last approval for PBS-subsidised biological medicine treatment in the most recent cycle
- to the date of the first application for initial treatment with a biological medicine under the new treatment cycle
There is no limit to the number of treatment cycles.
See Treatment breaks and failures for full details.
Patient baselines
When a patient qualifies for treatment, they have a measured and defined level of disease activity:
- this level becomes the patient’s baseline
- future applications are measured against the baseline to determine a response or failure to current treatment
- a patient who fails treatment with one medicine may wish to use this flare of disease to set a new baseline for future treatment to be measured against
The baseline measurement for psoriasis is the Psoriasis Area and Severity Index (PASI).
Note: if a patient is experiencing a flare, this does not always mean a change of baselines.
PASI
The PASI is a quantitative rating scale that measures the severity of psoriatic lesions based on the area coverage (as a percentage) and plaque appearance.
- Application forms include the relevant PASI for both groups of patients to be completed by prescribers
- The majority of patients listed on the program are assessed for response on their whole body PASI:
- Some patients have small patches just affecting the face, hand, or foot
- The face/hand/foot assessment is still referred to as a PASI (some may only refer to the whole body diagram as a PASI)
- Patients can be assessed on either the percentage coverage of the body as a whole, or the percentage coverage of the affected areas
- There are separate restrictions in place for each group of patients
Enquiries
Transfer enquiries about prescription arrangements to PBS Complex Drugs Programs and choose the option relevant to the condition treated.
The Resources page contains:
- application forms
- calculation sheets
- contact details
- restriction and item codes
- FAQs from Service Officers
- the PBS schedule
- Services Australia website link
Related links
Online Pharmaceutical Benefits Scheme (PBS) Authorities System (OPA System)
Process telephone Authority approval application
Processing and National Demand Allocation (PaNDA)
Processing Complex Authority Required Listings
Processing Written Authority requests
Written Authority Required Drugs