Can-Fite Provides Namodenoson Patent Update
29 Luglio 2024 - 1:00PM
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 announced an update related to the intellectual property (IP)
status of its lead drug candidate Namodenoson, currently being
developed for advanced liver cancer, pancreatic cancer and MASH.
The patents and patent applications cover
methods of treating the two solid tumors, liver and pancreatic
carcinoma by administering Namodenoson in an oral formulation as
well as treating MASH to improve liver steatosis, inflammation and
fibrosis. A patent application protecting the manufacturing of the
drug has recently been filed. Patent terms of granted patents and
patent application will have expiration dates of 2044 and beyond.
Can-Fite has already multiple approved patents and corresponding
applications in a variety of territories around the world,
including Europe and the US.
”We are delighted that the product protection of
Namodenoson in the area of oncology and MASH is broad and covers
the use and manufacturing of the drug for 20 years, and we look
forward to expanding this to other geographies”, said Pnina
Fishman, Ph.D., Can-Fite CSO and Chairperson.
Can-Fite is currently conducting a pivotal Phase
III study in advanced liver cancer and a Phase IIb study in MASH,
both in agreement with the FDA and EMA.
About Namodenoson
Namodenoson is a small orally bioavailable drug
that binds with high affinity and selectivity to the A3 adenosine
receptor (A3AR). Namodenoson is currently being evaluated in a
pivotal Phase III trial for advanced liver cancer, a Phase IIb
trial for the treatment of steatotic liver disease (SLD), and the
Company is planning a Phase IIa study in pancreatic cancer. A3AR is
highly expressed in diseased cells whereas low expression is found
in normal cells. This differential expression may be one of the
important factors that 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 metabolic
dysfunction-associated steatohepatitis (MASH), 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.canfite.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.
Contact
Can-Fite BioPharma
Motti Farbstein
info@canfite.com
+972-3-9241114
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