LuPIN Trial Interim Results Indicate Striking Survival Benefit
February 14 2020 - 8:00AM
Business Wire
Noxopharm (ASX: NOX) is pleased to announce positive interim
results from its LuPIN Phase 1/2 clinical trial. The data was
presented during a poster presentation at the ASCO Genitourinary
Cancers (GU) Symposium 2020 in San Francisco by St. Vincent’s
Hospital Sydney.
The LuPIN study is being conducted by St. Vincent’s Hospital
Sydney and is evaluating Noxopharm’s lead drug candidate, Veyonda®,
in combination with 177Lu-PSMA-617, in 56 patients with late-stage
metastatic castration-resistant prostate cancer (mCRPC).
“Today’s results are highly encouraging for patients, for
Noxopharm shareholders, and for the St. Vincent’s Hospital Sydney
team,” said Dr. Gisela Mautner, Noxopharm chief medical officer.
“The study reported an unprecedented median overall survival of
17.1 months. In a patient group that normally would have a survival
expectation of much less than this, such a result is astoundingly
good. The combination treatment of Veyonda® and 177Lu-PSMA-617 has
delivered a clinically meaningful and strong anti-cancer effect in
a high proportion of men and, importantly, continues to have an
excellent safety profile.”
All patients had received and failed two prior lines of therapy
(chemotherapy and androgen-signaling inhibitors), and most patients
(29 of 32) had failed a third line of therapy (another
chemotherapy) prior to entering the trial.
“The study investigators at St. Vincent’s Hospital Sydney
continue to do excellent work through the LuPIN trial and we are
pleased to support them,” Dr. Mautner added.
“Being able to deliver a meaningful anti-cancer response for at
least 50% of patients with Stage 4 for any form of cancer would be
a remarkable outcome,” said Noxopharm CEO Dr. Graham Kelly. “But it
is even more remarkable to do so in late-stage prostate cancer,
where the disease typically involves a substantial number of
secondaries in the skeleton, which are a significant and poorly
accessible tumor load. A median overall survival of 17.1 months is
remarkable for this novel radiosensitizing and immuno-oncology
drug.”
About Noxopharm
Noxopharm is a clinical-stage Australian oncology drug
development company with offices in Sydney and New York. The
Company has a primary focus on the development of Veyonda® and is
the major shareholder in the non-oncology drug development company,
Nyrada Inc. (ASX:NYR). Learn more at noxopharm.com.
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