# Kazia Therapeutics Reports 100% Clinical Benefit Rate in Initial Six Patients Treated for Advanced Triple-Negative Breast Cancer

- Link: https://www.thailand-business-news.com/pr-news/kazia-therapeutics-reports-100-clinical-benefit-rate-in-initial-six-patients-treated-for-advanced-triple-negative-breast-cancer
- Published: 2026-08-28T03:01:00+07:00
- Author: PR Newswire

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_Durable Complete Metabolic Response Ongoing Since November 2025_

_All Evaluable Patients Demonstrated Reductions in Metastasis-Associated CTC Clusters
and Terminally Exhausted T cells, With Median Reductions of 83% and 51% Respectively_

_No Treatment-Related Serious Adverse Events Observed_

SYDNEY, Aug. 28, 2026 /PRNewswire/ — [Kazia Therapeutics Limited](https://edge.prnewswire.com/c/link/?t=0&l=en&o=4761405-1&h=3234957468&u=https%3A%2F%2Fwww.kaziatherapeutics.com%2F&a=Kazia+Therapeutics+Limited)(
NASDAQ: KZIA) ("Kazia" or the "Company"), an oncology-focused biotechnology company
developing therapies that selectively reprogram cancer biology, restore anti-tumor
immunity and overcome treatment resistance, today announced new data showing its
lead asset, paxalisib, achieved a 100% clinical benefit rate in six evaluable patients
with Stage IV triple-negative breast cancer (TNBC). Five of the six patients achieved
an objective response – a measurable 30% or greater reduction in tumor burden after
treatment – including one complete response and four partial responses, resulting
in an objective response rate of 83 percent. The remaining patient achieved stable
disease. Importantly, these results were achieved with the convenience of oral dosing
and a favorable safety and tolerability profile, with no paxalisib-related serious
adverse events and no grade 3 or higher hyperglycemia, stomatitis or mucositis, 
toxicities commonly associated with PI3K/mTOR pathway inhibition.

"Metastatic triple-negative breast cancer is one of the toughest cancers to treat.
Historically, only [12 percent](https://edge.prnewswire.com/c/link/?t=0&l=en&o=4761405-1&h=21108310&u=https%3A%2F%2Fwww.cancer.gov%2Ftypes%2Fbreast%2Fbreast-cancer-types%2Ftriple-negative&a=12+percent)
of patients are alive five years after diagnosis. Once a patient’s disease progresses
on immunotherapy, options run out quickly," said Dr. John Friend, CEO, Kazia Therapeutics."
Across the six evaluable patients treated, every one of them has benefited, and 
we haven’t seen a single serious adverse event tied to paxalisib. We’ve also demonstrated
meaningful improvements in terminally exhausted T cells and drastic reductions in
circulating tumor cell (CTC) clusters, providing early evidence that paxalisib may
be addressing biological mechanisms associated with treatment resistance and metastasis.
These results strengthen our confidence in this program as we continue enrollment
in the Phase 1b trial."

Clinical responses were observed across a broad range of metastatic disease sites,
including lung, liver, bone, lymph node and central nervous system target lesions,
with responses emerging as early as approximately three months post-randomization.
Most notably, a 44-year-old woman with Stage IV TNBC achieved a complete metabolic
response and has had no evidence of disease since November 2025. Her response has
remained durable through the most recent assessment and has been accompanied by 
sustained and complete abolishment of CTC clusters and significant reduction in 
terminally exhausted CD8+ T cells, alongside overall improvement in markers of immune
function.

Translational analyses demonstrated reductions in terminally exhausted CD8+ T cells
across all six patients, with a median reduction of 51 percent within approximately
three weeks of treatment. These cells represent a dysfunctional population of cytotoxic
T cells that has lost its ability to recognize and kill cancer cells. Notably, total
CD8+ T cell counts remained unchanged, which suggests that paxalisib is not eliminating
these exhausted cells or replacing them with new ones. Instead, the existing cells
appear to be regaining function. Blood-based simultaneous multi-modal protein, RNA
and plasma profiling supported this finding, demonstrating increases in immune cell
populations associated with anti-tumor activity, reductions in markers of immune
exhaustion and evidence of PI3K-AKT pathway target engagement. The marker findings
provide evidence of improved overall immune function across all patients.

In parallel with the immune changes, all six patients demonstrated reductions in
circulating tumor cell clusters, which are aggressive groupings of tumor cells in
the bloodstream associated with metastatic spread. The median reduction was 83 percent
within six to seven weeks of treatment.

"Two of the biggest challenges in treating triple-negative breast cancer are the
dormant cancer cells that spread through the bloodstream, and an immune system too
exhausted to fight them. It’s rare to see a treatment influence both at the same
time. After years of studying this disease, it’s exciting to witness this in a clinical
setting. The circulating tumor cell clusters that seed new metastases are being 
suppressed, while the exhausted T cells needed to fight the cancer are recovering
function and showing signs of immune memory, which may translate to more durable
responses. These changes in the blood are tracking with what we are seeing on the
scans, which suggests our liquid biopsy approach may be capturing both the tumor’s
metastatic behavior and the immune system’s response to treatment in real time. 
It gives us a remarkable window into the disease, and we look forward to building
on these findings as the trial progresses," said Dr. Sudha Rao, Chief Scientific
Officer, Kazia Therapeutics.

These early biological findings represent what may be a first-in-class effect and
suggest that paxalisib’s therapeutic effect may extend beyond cytoplasmic PI3K/mTOR
inhibition. The rapid and consistent biological responses observed across all evaluable
patients support the hypothesis that paxalisib may exert dual influence by restoring
immune function and reducing metastatic dissemination, addressing two of the greatest
challenges in the treatment of triple-negative breast cancer and fundamental drivers
of cancer progression.

Enrollment in the Company’s ongoing Phase 1b study evaluating paxalisib in combination
with pembrolizumab (Keytruda^(®)) and chemotherapy in advanced metastatic TNBC is
expected to be completed by July 2027, with interim clinical updates anticipated
throughout 2026 and 2027.

**About Kazia Therapeutics**

Kazia Therapeutics Limited (NASDAQ: [**KZIA**](https://edge.prnewswire.com/c/link/?t=0&l=en&o=4761405-1&h=2082862204&u=https%3A%2F%2Fwww.prnewswire.com%2Fnews-releases%2Fkazia-therapeutics-appoints-james-levine-as-chief-financial-officer-302787604.html%23financial-modal&a=KZIA))
is an oncology-focused drug development company, based in Sydney, Australia. The
Company’s lead asset, paxalisib, is an investigational brain penetrant inhibitor
of the PI3K/Akt /mTOR pathway, which is being developed to treat multiple forms 
of cancer. Licensed from Genentech in late 2016, paxalisib is or has been the subject
of over 15 clinical trials. A completed Phase 2/3 study in glioblastoma (GBM AGILE)
was reported in 2024, and discussions are ongoing for designing and executing a 
pivotal registrational study in pursuit of a standard approval. Other clinical trials
involving paxalisib are ongoing in advanced breast cancer, brain metastases, diffuse
midline gliomas, and primary central nervous system lymphoma, with several of these
trials having reported encouraging interim data. Paxalisib was granted Orphan Drug
Designation for glioblastoma by the U.S. Food and Drug Administration (FDA) in February
2018, and Fast Track Designation (FTD) for glioblastoma in August 2020. Paxalisib
was also granted FTD in July 2023 for the treatment of solid tumor brain metastases
harboring PI3K pathway mutations in combination with radiation therapy.  Additionally,
paxalisib was granted Rare Pediatric Disease Designation and Orphan Drug Designation
by the FDA for diffuse intrinsic pontine glioma in August 2020 and for atypical 
teratoid / rhabdoid tumors in June 2022 and July 2022, respectively. Kazia is also
developing EVT801, a small molecule inhibitor of VEGFR3, which was licensed from
Evotec SE in April 2021. In addition to its clinical-stage programs, Kazia is advancing
NDL2, a potentially first-in-class intracellular PD-L1 protein degrader program 
targeting a newly identified mechanism of immunotherapy resistance and metastatic
progression, as well as MSETC, a potentially first-in-class SETDB1 inhibitor program
intended to restore immune signaling in tumors that have become resistant to immunotherapy,
including checkpoint inhibitors. Both programs are currently in preclinical development.
For more information, please visit [**www.kaziatherapeutics.com**](https://edge.prnewswire.com/c/link/?t=0&l=en&o=4761405-1&h=1180829521&u=http%3A%2F%2Fwww.kaziatherapeutics.com%2F&a=www.kaziatherapeutics.com)
or follow us on X @KaziaTx.

**Forward-Looking Statements**

This announcement may contain forward-looking statements, which can generally be
identified as such by the use of words such as "may," "will," "estimate," "future,""
forward," "anticipate," "expect," "plan," "believe," "potential," or other similar
words. Any statement describing Kazia’s future plans, strategies, intentions, expectations,
objectives, goals or prospects, and other statements that are not historical facts,
are also forward-looking statements, including, but not limited to, statements regarding:
the potential of paxalisib to provide clinical benefit, including objective responses,
to patients with advanced triple-negative breast cancer; the preliminary and interim
nature of the clinical, translational and biomarker data described in this announcement,
and expectations regarding the durability of any observed responses; the potential
for future data to alter initial and preliminary results from this early-stage clinical
trial, which is based on a small number of patients and is not designed or powered
to demonstrate statistical significance; the potential of paxalisib to restore anti-
tumor immune function and reduce metastasis-associated circulating tumor cell clusters;
the ability of translational and biomarker findings to predict clinical outcomes;
the timing of completion of enrollment in, and anticipated interim updates from,
the Company’s ongoing Phase 1b study of paxalisib in combination with pembrolizumab
and chemotherapy in advanced metastatic TNBC; and the timing and content of future
public disclosures regarding the Company’s clinical programs and development strategy.

Such statements are based on Kazia’s current expectations and projections about 
future events and future trends affecting its business and are subject to certain
risks and uncertainties that could cause actual results to differ materially from
those anticipated in the forward-looking statements, including risks and uncertainties
associated with: the development of early-stage therapeutic programs; the conduct
of clinical trials, including the ability to enroll patients and achieve anticipated
enrollment targets; the preliminary nature of preclinical data, which may not be
predictive of clinical results in humans; the preliminary nature of data from small,
open-label clinical studies, which are based on a small number of patients and may
not be predictive of results in a larger patient population or in later-stage or
final clinical trials; risks related to regulatory approvals; risks related to Kazia’s
reliance on third-party collaborators and clinical trial sites; risks related to
the Company’s ability to obtain, maintain and protect its intellectual property,
including the uncertainty of patent prosecution and the potential for third-party
challenges; risks related to the impact of global economic conditions; and risks
related to Kazia’s ability to maintain compliance with the applicable NASDAQ continued
listing requirements and standards. These and other risks and uncertainties are 
described more fully in Kazia’s Annual Report on Form 20-F filed with the SEC, and
in subsequent filings with the United States Securities and Exchange Commission.
Kazia undertakes no obligation to publicly update any forward-looking statement,
whether as a result of new information, future events, or otherwise, except as required
under applicable law. You should not place undue reliance on these forward-looking
statements, which apply only as of the date of this announcement.

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**Read the original article :** [Kazia Therapeutics Reports 100% Clinical Benefit Rate in Initial Six Patients Treated for Advanced Triple-Negative Breast Cancer ](http://www.prnasia.com/story/archive/5035665_AE35665_0?rand=184833)