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Can-Fite: Breakthrough Findings Demonstrate Namodenoson Anti-cancer and Protective Effect Mechanism in the Liver

Key Takeaway: Can-Fite BioPharma has revealed breakthrough findings concerning Namodenoson, a drug showing significant anti-cancer properties and protection in the liver through the signaling protein adiponectin. These findings will be presented at the IDDST-2024 congress in Shanghai. Namodenoson is currently undergoing pivotal Phase III trials for advanced liver cancer and has been granted Orphan Drug Designation and Fast Track Designation by regulatory bodies. The company is optimistic about its potential in treating various cancers and liver diseases.

Market Sentiment Analysis

POSITIVE FACTORS

  • Namodenoson shows promising anti-cancer effects and liver protection.
  • Breakthrough findings indicate a key mechanism involving adiponectin.
  • The drug is in pivotal Phase III studies, indicating progress towards approval.

Full Press Release Details

Can-Fite: Breakthrough Findings Demonstrate
Namodenoson Anti-cancer
and Protective Effect Mechanism in the Liver
Israel, June 24, 2024 -- Can-Fite BioPharma Ltd. (NYSE American: CANF) (TASE: CANF), a
biotechnology company advancing a pipeline of proprietary small molecule drugs that address oncological and inflammatory diseases,
today announces that company scientists came up with breakthrough findings showing that the anti-cancer and protective effects in
the liver are conferred via the signalling protein adiponectin. This very important positive cytokine plays a pivotal role in
regulating anti-inflammatory, anti-cancer, metabolic and insulin resistance. Namodenoson increases adiponectin production in
pre-clinical studies and in humans.
The data will be presented at the 20th Annual Congress of International
Drug Discovery Science & Technology, China Branch (IDDST-2024), September 12-14, Shanghai, China. This conference will host 300 leading
scientists from the academia and industry worldwide to discuss the latest developments in drug discovery and therapy.
"We are very much enthused by the
breakthrough findings that explain the dual mechanism of Namodenoson working as an anti-cancer agent in the liver and also inducing
a liver protective effect," stated Dr. Pnina Fishman, Can-Fite CSO & Chairperson.
Namodenoson is currently being evaluated in LiverationTM,
a pivotal Phase III study for advanced liver cancer that has been approved by both the U.S. Food and Drug Administration (FDA) and the
European Medicines Agency (EMA), and also in a Phase IIb study in patients with MASH.
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 and is expected to commence a pivotal Phase III. Can-Fite's cancer and
liver drug, Namodenoson, is being evaluated in a Phase IIb trial for the treatment of steatotic liver disease (SLD), a Phase III pivotal
trial for hepatocellular carcinoma (HCC), and the Company is planning a Phase IIa study in pancreatic 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 1,600 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 any resurgence of the COVID-19 pandemic and the war
between Israel and Hamas; 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 28, 2024 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 Namodenoson's mechanism of action?

Namodenoson acts as an anti-cancer agent by increasing adiponectin levels.

Which diseases are associated with Namodenoson?

Namodenoson is evaluated for liver cancer, NAFLD, and NASH treatment.

Where will Can-Fite present its findings on Namodenoson?

The findings will be presented at IDDST-2024 in Shanghai, China.

What phase studies is Namodenoson currently in?

Namodenoson is in Phase III for liver cancer and Phase IIb for MASH.

What is unique about Namodenoson's safety profile?

Namodenoson's selective binding results in an excellent safety profile.

Last updated: Jun 24, 2024