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Inhibition of Pancreatic Cancer by Namodenoson: Molecular Mechanism of Action Discovered by Can-Fite Scientists The anti-cancer effect in pancreatic carcinoma is mediated via a key signal transduction pathway According t

Key Takeaway: Can-Fite BioPharma has identified the molecular mechanism of action of its drug Namodenoson, which shows significant anti-cancer effects in pancreatic carcinoma by targeting the Wnt signaling pathway. This discovery came from pre-clinical studies involving pancreatic cancer patient cells and supports ongoing research into the drug's efficacy. Namodenoson is currently undergoing a Phase III study for liver cancer and has previously demonstrated success in treating liver cancer patients. The findings enhance the prospects for Namodenoson and inform future trial design.

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POSITIVE FACTORS

  • Discovery of the mechanism of action for Namodenoson in pancreatic cancer.
  • Demonstrated significant anti-cancer effect in pre-clinical studies.
  • Potential partnerships for further development of Namodenoson indicated by the findings.
  • Namodenoson's excellent safety profile noted from previous clinical experiences.

Full Press Release Details

Inhibition of Pancreatic Cancer by Namodenoson:
Molecular Mechanism of Action
Discovered by Can-Fite Scientists
PETACH TIKVA, Israel,
May 2, 2023 -- Can-Fite BioPharma Ltd. (NYSE American: CANF) (TASE: CANF), a biotechnology company
advancing a pipeline of proprietary small molecule drugs that address inflammatory, cancer and liver diseases, today announced that it
discovered the mechanism of action (MOA) involved with the significant anti-cancer effect of Namodenoson in pancreatic carcinoma. Namodenoson
de-regulates the Wnt signal transduction pathway, a key modulator of pancreatic carcinoma cell growth.
The discovery was made when analyzing results
from pre-clinical studies conducted on advanced pancreatic carcinoma patient cells exposed to Namodenoson, which had a significant anti-cancer
effect. This is the same MOA at work for Namodenoson in liver cancer.
Namodenoson is currently under a pivotal Phase
III study for the treatment of advanced liver cancer and has completely cleared cancer in an advanced liver cancer patient who remains
cancer-free 6 years after starting treatment.
"Knowing Namodenoson's mechanism of
action in pancreatic cancer is an important step in moving this indication toward potential partnerships. Our findings inform potential
dosage and study design and increase the probability of success in human trials," stated Can-Fite CEO Dr. Pnina Fishman.
The highest incidence
rates for pancreatic cancer are in Asia, Europe, and North America. According to the American Society of Clinical Oncology (ASCO), in
2020, an estimated 496,000 people were diagnosed with pancreatic cancer globally and an estimated 466,000 died from the disease. The 5-year
survival rate for people with pancreatic cancer in the U.S. is 11%. Acumen Research estimates the
global pancreatic cancer therapeutics market was valued at approximately $3.6 billion in 2021 and is projected to grow to approximately
$6.6 billion by 2030.
Namodenoson is a small orally bioavailable drug
that binds with high affinity and selectivity to the A3 adenosine receptor (A3AR). Namodenoson was evaluated in Phase II trials for two
indications, as a second line treatment for hepatocellular carcinoma, and as a treatment for non-alcoholic fatty liver disease (NAFLD)
and non-alcoholic steatohepatitis (NASH). A3AR is highly expressed in diseased cells whereas low expression is found in normal cells.
This differential effect accounts for the excellent safety profile of the drug.
About Can-Fite BioPharma Ltd.
Can-Fite BioPharma Ltd. (NYSE American: CANF)
(TASE: CANF) is an advanced clinical stage drug development Company with a platform technology that is designed to address multi-billion
dollar markets in the treatment of cancer, liver, and inflammatory disease. The Company's lead drug candidate, Piclidenoson recently reported
topline results in a Phase III trial for psoriasis. Can-Fite's liver drug, Namodenoson, is being evaluated in a Phase IIb trial for the
treatment of non-alcoholic steatohepatitis (NASH), and enrollment is expected to commence in a Phase III trial for hepatocellular carcinoma
(HCC), the most common form of liver cancer. Namodenoson has been granted Orphan Drug Designation in the U.S. and Europe and Fast Track
Designation as a second line treatment for HCC by the U.S. Food and Drug Administration. Namodenoson has also shown proof of concept to
potentially treat other cancers including colon, prostate, and melanoma. CF602, the Company's third drug candidate, has shown efficacy
in the treatment of erectile dysfunction. These drugs have an excellent safety profile with experience in over 1,500 patients in clinical
studies to date. For more information please visit: www.can-fite.com.
Forward-Looking Statements
This press release may contain forward-looking
statements, about Can-Fite's expectations, beliefs or intentions regarding, among other things, its product development efforts,
business, financial condition, results of operations, strategies or prospects. All statements in this communication, other than those
relating to historical facts, are "forward looking statements". Forward-looking statements can be identified by the use of
forward-looking words such as "believe," "expect," "intend," "plan," "may,"
"should" or "anticipate" or their negatives or other variations of these words or other comparable words or by
the fact that these statements do not relate strictly to historical or current matters. Forward-looking statements relate to anticipated
or expected events, activities, trends or results as of the date they are made. Because forward-looking statements relate to matters that
have not yet occurred, these statements are inherently subject to known and unknown risks, uncertainties and other factors that may cause
Can-Fite's actual results, performance or achievements to be materially different from any future results, performance or achievements
expressed or implied by the forward-looking statements. Important factors that could cause actual results, performance or achievements
to differ materially from those anticipated in these forward-looking statements include, among other things, our history of losses and
needs for additional capital to fund our operations and our inability to obtain additional capital on acceptable terms, or at all; uncertainties
of cash flows and inability to meet working capital needs; the initiation, timing, progress and results of our preclinical studies, clinical
trials and other product candidate development efforts; our ability to advance our product candidates into clinical trials or to successfully
complete our preclinical studies or clinical trials; our receipt of regulatory approvals for our product candidates, and the timing of
other regulatory filings and approvals; the clinical development, commercialization and market acceptance of our product candidates; our
ability to establish and maintain strategic partnerships and other corporate collaborations; the implementation of our business model
and strategic plans for our business and product candidates; the scope of protection we are able to establish and maintain for intellectual
property rights covering our product candidates and our ability to operate our business without infringing the intellectual property rights
of others; competitive companies, technologies and our industry; risks related to the COVID-19 pandemic and the Russian invasion of Ukraine;
risks related to not satisfying the continued listing requirements of NYSE American; and statements as to the impact of the political
and security situation in Israel on our business. More information on these risks, uncertainties and other factors is included from time
to time in the "Risk Factors" section of Can-Fite's Annual Report on Form 20-F filed with the SEC on March 30, 2023
and other public reports filed with the SEC and in its periodic filings with the TASE. Existing and prospective investors are cautioned
not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Can-Fite undertakes no obligation
to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise,
except as may be required by any applicable securities laws.

Frequently Asked Questions

What is the mechanism of action of Namodenoson?

Namodenoson inhibits pancreatic carcinoma by de-regulating the Wnt pathway.

What is the current status of Namodenoson in clinical trials?

Namodenoson is in a pivotal Phase III study for advanced liver cancer.

What makes Namodenoson's safety profile excellent?

Namodenoson targets A3 adenosine receptors, highly expressed in diseased cells.

What markets are expected to grow with pancreatic cancer therapeutics?

The global pancreatic cancer therapeutics market is projected to reach $6.6 billion by 2030.

Who developed Namodenoson?

Namodenoson was discovered by Can-Fite BioPharma Ltd. scientists.

Last updated: May 2, 2023