SOTAGLIFLOZIN

Information current as at: 1 July 2026

PBAC meeting date: November 2026
Legend: Completed N In progress Not applicable N Yet to commence

Submission Details

Brand name:
  • Inpefa®
Form and strength:
  • Tablet 200 mg
  • Tablet 400 mg
Submission sponsor:
VIATRIS PTY LTD
Condition/indication:
(therapeutic use)
  • Heart failure
Listing requested:
To request listing of sotagliflozin in adult patients recently hospitalised for acute decompensated heart failure, regardless of left ventricular ejection fraction (LVEF) and with or without type 2 diabetes. Sotagliflozin is proposed to be initiated during hospitalisation, or within 14 days of discharge, and continued long-term in the community.
Funding program:
PBS General Schedule
Request authority level:
Authority Required (STREAMLINED)
PBAC Submission type:
New PBS listing (–)
Comment:
--
Other PBAC consideration:
--

Progress Details

Submission received for:
November 2026 PBAC meeting
2Opportunity for consumer comment:
Open 22/07/2026 and close 16/09/2026 (see PBS Website)
3PBAC meeting:
Has not yet occurred
4PBAC outcome published:
Pending PBAC outcome (see PBAC Outcomes)
5Lodgement of required documentation:
6Agreement to listing arrangements:
Has not yet commenced
7Government processes:
Has not yet commenced
8Medicine listed on the PBS:
Has not yet occurred
Glossary

PBAC Outcome

PBAC Recommendation:
Please see the Outcomes from the relevant meeting for more information
Case ID
a1307
Page last updated
23 July 2026
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