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Can-Fite: Patient with Decompensated Liver Cirrhosis Successfully Undergoes Liver Transplantation Following Treatment with Namodenoson

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Can-Fite (NYSE American: CANF) reported that a patient with advanced decompensated liver cirrhosis treated with Namodenoson under compassionate use achieved clinical stabilization and subsequently underwent a successful liver transplantation on Feb 5, 2026. The single-case outcome suggests Namodenoson may serve as a supportive bridge to transplant.

The drug is an oral A3 adenosine receptor agonist being evaluated in advanced liver diseases, with prior studies showing a favorable safety profile.

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News Market Reaction

+5.20%
3 alerts
+5.20% News Effect
+3.3% Peak Tracked
+$170K Valuation Impact
$3M Market Cap
0.0x Rel. Volume

On the day this news was published, CANF gained 5.20%, reflecting a notable positive market reaction. Argus tracked a peak move of +3.3% during that session. Our momentum scanner triggered 3 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $170K to the company's valuation, bringing the market cap to $3M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Decompensated cirrhosis patients: 10.6 million people Liver cirrhosis market 2024: $7.6 billion Liver cirrhosis market 2031: more than $15 billion +2 more
5 metrics
Decompensated cirrhosis patients 10.6 million people Global burden in 2017
Liver cirrhosis market 2024 $7.6 billion Global liver cirrhosis treatment market in 2024
Liver cirrhosis market 2031 more than $15 billion Projected global liver cirrhosis treatment market by 2031
Transplant wait time over five years Some patients wait over five years for a liver transplant
Publication year estimate 2017 Year of global decompensated cirrhosis prevalence estimate

Market Reality Check

Price: $4.26 Vol: Volume 16,116 is well bel...
low vol
$4.26 Last Close
Volume Volume 16,116 is well below the 20-day average of 65,758 (about 0.25x). low
Technical Shares at $4.11 are trading below the 200-day MA at $13.20 and far under the $46.60 52-week high.

Peers on Argus

Ahead of this news, CANF was down 0.25%, while several biotech peers like ADAP, ...
1 Down

Ahead of this news, CANF was down 0.25%, while several biotech peers like ADAP, BIVI, CYCC, and MTVA also traded lower (-1.59% to -17.57%). NXTC was a notable outlier, up 3.14%, suggesting a generally weak biotech tape with some stock-specific exceptions.

Historical Context

5 past events · Latest: Jan 20 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Jan 20 Clinical enrollment Positive -0.3% Completed patient enrollment for Phase 2a Namodenoson pancreatic cancer study.
Dec 26 Patent grant Positive +18.6% Brazilian patent granted for A3AR agonist use in sexual dysfunction.
Dec 23 Reverse split Negative -1.7% Announced 1-for-3,000 reverse split and ADS ratio change.
Dec 16 Clinical & financial update Positive +9.1% Provided update on Phase III/II trials and disclosed cash and recent financings.
Nov 26 Conference presentation Neutral +0.0% Announced NobleCon21 presentation on advanced-stage drug pipeline.
Pattern Detected

Recent clinically focused updates and IP wins have often coincided with positive or neutral price reactions, while corporate structure changes like the reverse split saw modest pressure.

Recent Company History

Over the past few months, Can-Fite highlighted multiple Namodenoson milestones and corporate actions. On Dec 16, 2025, it detailed advanced liver and oncology trials plus financing, with shares up 9.06%. A Brazilian sexual dysfunction patent on Dec 26, 2025 saw a 18.64% gain. By contrast, the 1-for-3,000 reverse split announced on Dec 23, 2025 coincided with a mild decline. The Jan 20, 2026 Phase 2a pancreatic enrollment completion drew a flat-to-slightly-negative move, underscoring mixed but often constructive reactions to clinical news.

Market Pulse Summary

The stock moved +5.2% in the session following this news. A strong positive reaction aligns with Can...
Analysis

The stock moved +5.2% in the session following this news. A strong positive reaction aligns with Can-Fite’s history of sizable moves on clinically supportive news, such as prior patent and pipeline updates with reactions up to 18.64%. This single-patient Namodenoson case adds to liver-disease narratives but remains anecdotal. With shares still far below the $46.60 52‑week high and below the $13.20 200‑day MA, investors may weigh enthusiasm against the need for larger, controlled datasets.

Key Terms

compassionate use, A3 adenosine receptor, anti-inflammatory, anti-fibrotic, +1 more
5 terms
compassionate use regulatory
"The patient received Namodenoson treatment under a compassionate use framework"
Compassionate use is a regulated program that lets patients access an experimental drug or medical device outside a formal clinical trial when no approved treatment is available. For investors, it matters because such access can provide early real-world safety and demand signals, affect regulatory relationships and public perception, and slightly alter near-term revenue prospects or liability exposure — similar to a company offering a prototype to select customers before full approval.
A3 adenosine receptor medical
"Namodenoson is an orally bioavailable A3 adenosine receptor (A3AR) agonist"
A3 adenosine receptor is a specific protein on the surface of certain cells that acts like a lock responding to the natural molecule adenosine; when activated it influences inflammation, blood flow, and cell survival. For investors, it matters because drugs that selectively target this receptor can change disease outcomes or side-effect profiles, so clinical trial results or regulatory decisions about such drugs can materially affect biotech valuations and the potential market for new therapies.
anti-inflammatory medical
"agonist with anti-inflammatory and anti-fibrotic properties"
A substance or treatment that reduces swelling, redness, pain, or immune overreaction in the body. Investors care because anti-inflammatory products represent a large and steady part of healthcare spending—new or improved treatments can expand markets, change prescribing patterns, lower complication rates, or affect reimbursement and regulatory review, much like a more efficient tool replacing an older one in a toolbox.
anti-fibrotic medical
"agonist with anti-inflammatory and anti-fibrotic properties"
Anti-fibrotic describes a drug or therapy that slows, stops, or reverses fibrosis—the buildup of scar tissue in organs (such as lungs, liver, or heart) that stiffens tissue and reduces function. For investors, anti-fibrotic treatments matter because they address chronic conditions with large unmet needs and potential long-term markets; like repairing a clogged pipe before it bursts, successful therapies can preserve organ function, affect patient outcomes, and drive regulatory, clinical and commercial value.
hepatocellular carcinoma medical
"being evaluated in advanced liver diseases, including MASH and hepatocellular carcinoma."
Hepatocellular carcinoma is the most common form of primary liver cancer, arising from the main functional cells of the liver. For investors it matters because its serious health impact drives demand for diagnostic tests, treatments and long-term care; progress in trials or approvals can change a drugmaker’s revenue outlook much like a successful product launch can reshape a company’s future.

AI-generated analysis. Not financial advice.

Namodenoson Provided Clinical Stabilization as a Potential Bridge to Transplant in Advanced Liver Failure

Ramat Gan, Israel, Feb. 05, 2026 (GLOBE NEWSWIRE) -- Can-Fite BioPharma Ltd. (NYSE American: CANF) (TASE: CANF), a biotechnology company developing a pipeline of proprietary small molecule drugs targeting oncological and inflammatory diseases, today announced that a patient with advanced decompensated liver cirrhosis who was treated with Namodenoson subsequently underwent a successful liver transplantation.

The patient received Namodenoson treatment under a compassionate use framework while suffering from liver disease and complications consistent with decompensated cirrhosis. Throughout the treatment period, Namodenoson contributed to clinical stabilization, allowing the patient to remain a suitable candidate for liver transplantation until a compatible donor organ became available, ultimately resulting in a successful, life-saving liver transplantation. While this is a single case, the outcome suggests a potential supportive role for Namodenoson in patients with severe liver dysfunction awaiting transplantation. Due to the ongoing shortage of donor organs, many patients with decompensated cirrhosis deteriorate rapidly and, tragically, do not survive long enough to receive a suitable transplant, highlighting the importance of therapies that may help maintain stability during this critical period.

Namodenoson is an orally bioavailable A3 adenosine receptor (A3AR) agonist with anti-inflammatory and anti-fibrotic properties, which has demonstrated a favourable safety profile in previous clinical studies. The drug is currently being evaluated in advanced liver diseases, including MASH and hepatocellular carcinoma.

“This case represents an encouraging clinical observation in a patient with advanced liver disease,” stated Prof. Ohad Etzion, Chief of Gastroenterology and Liver Diseases at Soroka Medical Center in Israel. “Although individual cases must be interpreted with caution, the ability to maintain clinical stability in such a fragile patient population is highly meaningful. We believe these findings support the continued clinical development of Namodenoson in  liver disorders where treatment options remain extremely limited.”

In 2017, an estimated 10.6 million people globally were affected by decompensated cirrhosis, and the available treatment options remain scarce, especially for patients who have reached the advanced stages of the disease. Highlighting the urgent need for new therapies, the American Liver Foundation has stated that there are more patients in need of a liver transplant than available organs, with some patients waiting over five years for a transplant. The global liver cirrhosis treatment market is projected to grow from approximately $7.6 billion in 2024 to more than $15 billion by 2031.

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 Metabolic Dysfunction-associated Steatohepatitis (MASH), and in 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 reported topline results in a Phase III trial for psoriasis and commenced a pivotal Phase III trial. Can-Fite's liver drug, Namodenoson, is being evaluated in a Phase III trial for hepatocellular carcinoma (HCC), a Phase IIb trial for the treatment of MASH, and in 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: https://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 April 14, 2025 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


FAQ

What happened in Can-Fite's Feb 5, 2026 announcement about Namodenoson (CANF)?

A patient with decompensated cirrhosis treated with Namodenoson achieved stabilization and later received a successful liver transplant. According to the company, this single compassionate-use case suggests Namodenoson may help maintain transplant eligibility while awaiting a donor organ.

How did Namodenoson reportedly help the liver transplant candidate in the CANF case?

Namodenoson reportedly contributed to clinical stabilization that preserved transplant candidacy until a donor was available. According to the company, the drug's anti-inflammatory and anti-fibrotic A3AR activity was associated with maintaining the patient's condition during the waiting period.

Does the Can-Fite (CANF) announcement mean Namodenoson is proven effective for decompensated cirrhosis?

No; the outcome is a single compassionate-use observation and not definitive evidence of efficacy. According to the company, the case is encouraging but requires controlled clinical studies to establish safety and effectiveness in this population.

What is Namodenoson and which liver conditions is Can-Fite (CANF) studying it for?

Namodenoson is an oral A3 adenosine receptor agonist with anti-inflammatory and anti-fibrotic properties. According to the company, it is being evaluated in advanced liver diseases including MASH and hepatocellular carcinoma.

What are the implications for transplant patients from Can-Fite's Namodenoson case (CANF)?

The case suggests a potential supportive role for maintaining stability in fragile patients awaiting transplant, possibly reducing dropouts. According to the company, broader clinical data are needed to determine whether this observation translates into a reliable bridge-to-transplant therapy.
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