DURVALUMAB
Information current as at: 1 July 2026
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
-
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
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.
