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KZIANasdaq

KAZIA THERAPEUTICS LTD

Biopharma developer (SEC filing verified)·Phase 1·Sydney, NSW, Australia·CEO: Dr. John Edwin Friend II, M.D.
Oncology

KZIA evidence brief

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BioSniper AI · KZIA

Kazia Therapeutics Ltd is a clinical-stage oncology company developing two small-molecule drug candidates, Paxalisib (PI3K/Akt/mTOR inhibitor) and EVT801 (VEGFR3 inhibitor), with a going-concern uncertainty and limited cash resources.

Key risk: Going-concern uncertainty

Market Cap

$155.2M

Cash Runway

Lead Asset

Next Catalyst

Financial data as of Dec 31, 2025.

Tracking 1 clinical trial for KAZIA THERAPEUTICS LTD.

AI OverviewAI overview is shown in English only.

Kazia Therapeutics Ltd is a clinical-stage oncology company developing two small-molecule drug candidates, Paxalisib (PI3K/Akt/mTOR inhibitor) and EVT801 (VEGFR3 inhibitor), with a going-concern uncertainty and limited cash resources.

  • Lead programs include Paxalisib (PI3K/Akt/mTOR inhibitor) and EVT801 (VEGFR3 inhibitor) [sec · filed 2025-11-07].
  • As of 2025-12-31, the company reported cash & equivalents of $69.5M, no revenue, and a net loss of -$20.7M [sec].
  • As of 30 June 2025, accumulated losses were A$134.8M and cash was A$4.3M [sec · filed 2025-11-07].
  • There is substantial doubt about the company's ability to continue as a going concern [sec · filed 2025-11-07].
  • Plans for a Phase 2 trial are on hold while exploring regional and strategic partnerships [sec · filed 2025-11-07].

What works

  • Paxalisib targets the clinically validated PI3K/Akt/mTOR pathway in oncology [sec · filed 2025-11-07].
  • The company has two product candidates in clinical trials, providing multiple shots on goal [sec · filed 2025-11-07].
  • Anticipated milestones for fiscal year 2026 include completion of enrollment in a Phase 1b trial of Paxalisib in TNBC and publication of expanded-access data [sec · filed 2025-11-07].

What to weigh

  • The company has a going-concern uncertainty and expects to consume cash and incur operating losses for the foreseeable future [sec · filed 2025-11-07].
  • As of 30 June 2025, accumulated losses were A$134.8M, and cash was only A$4.3M (though later reported $69.5M as of 2025-12-31) [sec · filed 2025-11-07].
  • Failure of either product candidate to show benefit could materially and adversely affect business continuity [sec · filed 2025-11-07].
  • The company may not be able to secure additional funding on acceptable terms, which could force delays or reductions in clinical programs [sec · filed 2025-11-07].

From the filings

Quoted directly from source documents.

  • Going-concern uncertainty

    There is substantial doubt about our ability to continue as a going concern, which may hinder our ability to obtain future financing.

    SEC filings · November 7, 2025

  • Lead programs are Paxalisib and EVT801

    The Company's lead programs include Paxalisib (formerly GDC-0084), a small molecule inhibitor of the PI3K/Akt/mTOR pathway, and EVT801, a small molecule selective inhibitor of vascular endothelial growth factor receptor 3 ("VEGFR3").

    SEC filings · November 7, 2025

  • Accumulated losses as of 30 June 2025

    as of 30 June 2025, we had accumulated losses of A$134.8 million.

    SEC filings · November 7, 2025

  • Phase 2 trial plans on hold

    Plans for phase 2 clinical trial are on hold while exploring regional and strategic partnerships.

    SEC filings · November 7, 2025

Risks & what to watch (4)

Key risks

  • Going-concern uncertaintySubstantial doubt about ability to continue as a going concern may hinder financing [sec · filed 2025-11-07].
  • Clinical trial failure riskFailure of either product candidate to show benefit could materially and adversely affect business [sec · filed 2025-11-07].
  • Need for additional fundingCompany expects to consume cash and will need additional capital; may not obtain on acceptable terms [sec · filed 2025-11-07].
  • No revenue in foreseeable futureCompany does not anticipate generating revenue from product sales for the foreseeable future [sec · filed 2025-11-07].

What to watch

  • Completion of enrollment in the Phase 1b trial of Paxalisib in TNBC, anticipated in fiscal year 2026 [sec · filed 2025-11-07].
  • Preliminary analyses from expanded-access Paxalisib data in TNBC, expected in fiscal year 2026 [sec · filed 2025-11-07].
  • Progress on regional and strategic partnerships for the Phase 2 trial [sec · filed 2025-11-07].
  • Ability to secure additional financing to fund ongoing R&D and operations [sec · filed 2025-11-07].

Sources: SEC filings · Generated August 29, 2026 · How we verify sources →

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Evidence & data

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

16

Total value held

$3.5M

Showing top 10 of 16 institutional holders of KAZIA THERAPEUTICS LTD. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
3.6%
Days to cover
1.4
Shares short
408,115
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

KZIA short interest

Frequently asked questions

What is the AI investment thesis for KAZIA THERAPEUTICS LTD?

Kazia Therapeutics Ltd is a clinical-stage oncology company developing two small-molecule drug candidates, Paxalisib (PI3K/Akt/mTOR inhibitor) and EVT801 (VEGFR3 inhibitor), with a going-concern uncertainty and limited cash resources.

Who is the CEO of KAZIA THERAPEUTICS LTD?

Dr. John Edwin Friend II, M.D. is the chief executive officer of KAZIA THERAPEUTICS LTD (KZIA).

Where is KAZIA THERAPEUTICS LTD headquartered?

KAZIA THERAPEUTICS LTD (KZIA) is headquartered in Sydney, NSW, Australia.

What therapeutic areas does KAZIA THERAPEUTICS LTD focus on?

KAZIA THERAPEUTICS LTD develops therapies across Oncology.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.