DURVALUMAB

Information current as at: 1 July 2026

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

Submission Details

Brand name:
  • Imfinzi®
Form and strength:

Please search for and view the meeting agenda from the relevant meeting for more information

Submission sponsor:
ASTRAZENECA PTY LTD
Condition/indication:
(therapeutic use)
  • Gastric cancer (GC) or gastro-oesophageal junction cancer (GOJC)
Listing requested:
Please see meeting agenda for more information
Funding program:
PBS Section 100 (Efficient Funding of Chemotherapy Program)
Request authority level:
Please see meeting agenda for more information
PBAC Submission type:
Change to existing listing (Category 2)
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:
15/04/2026
Lodgement of required documentation:
07/05/2026
Acceptance of complete documentation:
Accepted
Agreement to listing arrangements:
Commenced on 10/06/2026
Status:
Finalised
7Government processes:
Commenced on 19/06/2026
8Medicine listed on the PBS:
Has not yet occurred

PBAC Outcome

PBAC Recommendation:

The PBAC recommended the listing of durvalumab for use both before and after surgery in patients with gastric or gastroesophageal junction cancers (GC/GOJC) who are eligible for the chemotherapy combination of fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) before surgery. The PBAC acknowledged that these cancers are challenging to treat and have significant impacts on quality of life despite currently available treatment options. The PBAC was satisfied that addition of durvalumab to existing treatment before and after surgery reduces the risk of the cancer returning and helps patients with GC/GOJC live longer when compared with current standard treatments. The PBAC considered durvalumab would be cost effective with a price reduction to reflect evidence of benefit, cost of other medicines it had recommended for use before and after surgery, uncertainty about subsequent immunotherapy, and the changing landscape with respect to PBS listings for immunotherapy. The PBAC considered that with some minor adjustments to the economic modelling, the estimated cost to the government was reasonable.

Public Summary Document:
Not yet available

Case ID
a1158
Page last updated
30 June 2026
v.9.19