Noxopharm Pre-clinical Study Confirms Survival Advantage of Combination LuPSMA Therapy in Prostate Cancer
12 August 2021 - 10:00PM
Business Wire
Australian clinical-stage drug development company Noxopharm
Limited (ASX:NOX) has reported pre-clinical data confirming a
survival benefit of adding Veyonda® to 177lutetium-PSMA-617
(LuPSMA) treatment in prostate cancer. This result validates the
survival benefit of the same combination seen in a recently
completed Phase I/II trial of Veyonda in men with end-stage
metastatic castrate-resistant prostate cancer (mCRPC).
Pre-Clinical Data Confirm Survival Benefit of Combination
Treatment
A study in mice bearing human prostate cancer xenografts, and
led by Professor Kristofer Thurecht, Ph.D., at The University of
Queensland, confirmed a potent ability of Veyonda to enhance the
cancer-killing effect of LuPSMA treatment.
“The combination of Veyonda with LuPSMA exhibited an impressive
synergistic therapeutic response, with sustained and almost
complete regression of the tumor and minimally observed systemic
toxicity,” said Dr. Thurecht. “This combined response was not
observed in any of the animals treated with monotherapy.”
Results Support Survival Benefit Found in Phase I/II Clinical
Trial
The results of Noxopharm’s LuPIN Phase I/II clinical trial were
published recently in The Journal of Nuclear Medicine and showed a
median overall survival of 19.7 months with combination therapy in
men with mCRPC with no remaining treatment options.
“The LuPIN study was a non-randomized study, so the question
remained of how much the remarkable outcome of 19.7 months was due
to the combination effect versus LuPSMA monotherapy alone,” said
Noxopharm CEO, Graham Kelly. “The pre-clinical study results
confirmed that LuPSMA monotherapy had an impressive anti-cancer
effect on tumor growth — but when Veyonda was added, the tumors
mostly disappeared.”
About Noxopharm
Noxopharm Limited (ASX:NOX) is an Australian clinical-stage drug
development company focused on the treatment of cancer and cytokine
storm (septic shock).
Veyonda® is the Company’s first pipe-line drug candidate
currently in Phase 2 clinical trialling. Veyonda® has two
main drug actions – a moderating effect on the
ceramide/sphingosine-1-phosphate balance and inhibition of STING
signalling. Activity against the former target contributes to its
dual-acting oncotoxic and immunomodulatory functions designed to
enhance the effectiveness and safety of standard oncology
treatments, i.e., chemotherapies, radiation therapies and immune
checkpoint inhibitors. Activity against the latter target provides
an anti-inflammatory effect, as well as contributing to an
anti-cancer action, but also potentially blocking septic shock.
Noxopharm is running comprehensive drug discovery programs in
both oncology and inflammation, and is the major shareholder of US
biotechnology company, Nyrada Inc (ASX:NYR), active in the areas of
drug development for cardiovascular and neurological diseases.
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Lindsey Langemeier SCORR Marketing 402-405-4269
lindsey@scorrmarketing.com
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