TILDRAKIZUMAB
Information current as at: 1 July 2026
Submission Details
- Brand name:
-
- Ilumya®
- Form and strength:
-
Please search for and view the meeting agenda from the relevant meeting for more information
- Submission sponsor:
- SUN PHARMA ANZ PTY LTD
- Condition/indication:
(therapeutic use) -
- Severe chronic plaque psoriasis
- Listing requested:
- Please see meeting agenda for more information
- Funding program:
- PBS General Schedule
- Request authority level:
- Please see meeting agenda for more information
- PBAC Submission type:
- Change to existing listing (Category 3)
- Comment:
- --
- Other PBAC consideration:
- --
Progress Details
-
Submission received for: - March 2026 PBAC meeting
-
Opportunity for consumer comment: - Open 19/11/2025 and close 21/01/2026 (see PBS Website)
-
PBAC meeting: - Held on 11/03/2026
-
Lodgement of required documentation: - 29/04/2026
-
Acceptance of complete documentation:
- Accepted
-
Agreement to listing arrangements: - Commenced on 11/06/2026
-
Status:
- Finalised
-
7Government processes:
- Commenced on 12/06/2026
-
8Medicine listed on the PBS:
- Has not yet occurred
PBAC Outcome
The PBAC recommended tildrakizumab 200 mg (100 mg/mL injection, 2 x 1 mL syringe) for the treatment of severe chronic plaque psoriasis. The PBAC considered that tildrakizumab 200 mg would result in the same outcomes (i.e. efficacy and safety) compared with tildrakizumab 100 mg. The PBAC noted and welcomed input from the Australasian College of Dermatologists, who advocated for increasing the maintenance dose to 200 mg to provide an opportunity to improve outcomes in patient with severe disease or obesity. The PBAC considered that treating doctors, at their discretion, may escalate the dose of tildrakizumab to 200 mg in any patient who has responded adequately to the most recent course of tildrakizumab 100 mg, noting that the magnitude of any improved outcomes may be modest.
