Recent Updates
Recently added Catalysts
CANF Positive Sentiment Score: 80/100

Can-Fite Issues Business Update: All Clinical Programs and Business Development Activities Remain Solidly on Track Company management updates about ongoing activities and progress

Key Takeaway: Can-Fite BioPharma Ltd. has updated its stakeholders that all clinical programs and business development activities are on track. The company's pipeline includes pivotal Phase III studies in advanced liver cancer and psoriasis, with a strong focus on international collaboration and partnerships. Management highlighted increased interest in its drug candidates, Namodenoson and Piclidenoson, positioning them for potential future deals. Can-Fite is also leveraging AI and ML to enhance drug development, particularly in the rare genetic diseases market.

Market Sentiment Analysis

POSITIVE FACTORS

  • All clinical and business development activities are progressing as planned.
  • Strong interest in drug candidates Namodenoson and Piclidenoson from potential pharma partners.
  • Entering the rare genetic diseases market presents an estimated $100 million opportunity.
  • Use of AI and ML to expedite drug development could significantly reduce costs.

Full Press Release Details

Can-Fite Issues Business Update: All
Clinical Programs and Business Development Activities Remain Solidly on Track
Company management updates about ongoing
activities and progress
PETACH TIKVA, Israel, November 01, 2023 -- 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 confirmed that all of the Company's clinical and business development activities
are ongoing and proceeding by both its Israeli and US based staff.
"Can-Fite remains focused and stronger than
ever in our purpose to bring medications to market that improve and save lives. We are working closely with our US based executives, Dr.
Bill Kerns and Dr. Michael Silverman, with all our consultants and our collaboration partners in Canada, Europe, the US, China and South
Korea. All the investigators participating in the conductance of the clinical studies are working full force and continue patient enrolment
for the ongoing advanced clinical studies," stated Dr. Pnina Fishman, Can-Fite's Chief Scientific Officer and Executive Chairman.
"Our business development activities are robust and we are receiving a high level of interest, in both Namodenoson and Piclidenoson,
which we believe may lead to new pharma partnerships in the near-term."
The Company's advanced-stage clinical pipeline
includes two pivotal Phase III studies: an ongoing trial in advanced liver cancer and a psoriasis study that has been cleared by the U.S.
Food and Drug Administration as well as the European Medicines Agency and is expected to commence enrollment shortly. Phase II trials
include an ongoing study for steatotic liver disease (SLD), formerly known as NASH, and preparatory work is underway for a Phase IIa trial
in pancreatic cancer.
Can-Fite's latest value-driving developments
include its entry into the rare genetic diseases market with Piclidenoson which was found to be effective in pre-clinical studies for
the treatment of Lowe Syndrome, an estimated $100 million treatment market in the U.S. alone in which there is no therapeutic treatment
option available. Through a partnership with Collaborations Pharmaceuticals, Can-Fite will now utilize artificial intelligence (AI) and
machine learning (ML) techniques to identify next-generation A3 adenosine receptor drug agonists and significantly reduce development
time and costs of bringing such drugs to market.
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 the COVID-19 pandemic and the Russian invasion of Ukraine;
risks related to not satisfying the continued listing requirements of NYSE American; and security, political and economic instability
in the Middle East that could harm our business, including due to the current war between Israel and Hama. 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 updates has Can-Fite provided about its clinical programs?

Can-Fite confirmed that all clinical and business development activities are ongoing and progressing well.

Which diseases does Can-Fite's pipeline target?

Can-Fite's drugs address oncological and inflammatory diseases, including liver cancer and psoriasis.

What is notable about Piclidenoson?

Piclidenoson has shown effectiveness for treating Lowe Syndrome, a rare genetic condition.

What clinical trials are currently in progress?

Can-Fite is conducting Phase III trials for advanced liver cancer and psoriasis.

How is Can-Fite using AI in its development process?

Can-Fite collaborates with Collaborations Pharmaceuticals to use AI for drug development efficiency.

Last updated: Nov 1, 2023