TILDRAKIZUMAB

Information current as at: 1 July 2026

Legend: Completed N In progress Not applicable N Yet to commence

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
PBAC outcome published:
Recommended (see PBAC Outcomes)
Notice of intent submitted:
03/04/2026
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

PBAC Recommendation:

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.

Public Summary Document:
Not yet available

Case ID
a1185
Page last updated
30 June 2026
v.9.19