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CanFite BioPharma

Full company profile

uuid0004fo3

Namestring
CanFite BioPharma
Legal namestring
Can-Fite BioPharma Ltd.
Websiteurl
canfite.com
Company typeenum
Public
Founded yearint
1994
Descriptiontext

Can-Fite BioPharma Ltd. is an Israeli clinical-stage biopharmaceutical company founded in 1994 and listed on NYSE American and the Tel Aviv Stock Exchange (ticker: CANF). The company develops orally bioavailable small molecule agonists targeting the Gi protein-associated A3 adenosine receptor (A3AR), a receptor that is highly expressed in inflammatory, cancer, and other pathological cells but minimally expressed in healthy cells. Compounds bind with nanomolar affinity to A3AR and modulate the NF-kB and Wnt signal transduction pathways to deliver anti-inflammatory and anti-cancer effects, with safety data accumulated across more than 1,600 patients in clinical studies.

The clinical pipeline comprises three core candidates and one preclinical program. Piclidenoson (CF101) is an A3AR agonist in pivotal Phase III for moderate-to-severe plaque psoriasis following positive Phase III COMFORT-1 topline data. Namodenoson (CF102) is the lead oncology asset, in pivotal Phase III for advanced hepatocellular carcinoma, Phase IIb for MASH, and Phase IIa for pancreatic cancer; it has received FDA Orphan Drug Designation for HCC and pancreatic cancer plus FDA Fast Track Designation for second-line HCC. CF602 is an A3AR allosteric modulator in preclinical development for erectile dysfunction, particularly for diabetic patients and PDE5 non-responders, and a cannabinoid program targets the endocannabinoid system. The company pursues a pure out-licensing model, granting exclusive regional development and commercialization rights to specialized pharmaceutical distributors in exchange for upfront payments, regulatory and sales milestones, and royalties on net sales.

Can-Fite generates revenue from licensing agreements rather than direct product sales. Current commercial partners include Ewopharma (Central Eastern Europe), CMS (China/Hong Kong/Macao/Taiwan), Chong Kun Dang (South Korea), Cipher Pharmaceuticals (Canada), Gebro Pharma (Switzerland/Spain/Austria), Kyongbo Pharm (South Korea), and Vetbiolix (worldwide veterinary). The Ewopharma agreement alone includes a $2.25 million upfront payment, up to $40.45 million in milestones, and 17.5% royalties on net sales; the Vetbiolix veterinary deal is potentially worth up to $325 million. FY2025 revenue was $0.41 million against a $9.83 million net loss, with operations funded by recurring equity raises totaling approximately $19 million between November 2023 and March 2026, led by H.C. Wainwright & Co.

Short descriptiontext

Can-Fite BioPharma is an Israeli clinical-stage biopharmaceutical company that develops orally bioavailable small molecule A3 adenosine receptor (A3AR) agonists for oncology (liver and pancreatic cancer), inflammatory diseases (psoriasis), and metabolic disorders (MASH, obesity), generating revenue through regional out-licensing partnerships rather than direct commercialization.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersPetah Tiqva, Israel
HQ citystring
Petah Tiqva
HQ countrystring
Israel
HQ regionstring
Middle East
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage biopharmaceutical, A3 adenosine receptor, small molecule therapeutics, oncology drug development, anti-inflammatory drug pipeline
Industry2 codes
1Gastroenterology & Hepatology Pharmaceuticals
CodeHLAIAAAIPrimaryNo
2Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health)
CodeHLAIAAAJPrimaryNo
NAICS code3 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Pharmaceutical Preparation Manufacturing325412
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code3 codes
  • Pharmaceutical Preparations2834
  • Medicinal Chemicals & Botanical Products2833
  • Services-Commercial Physical & Biological Research8731
Product category
Clinical-Stage Biopharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Licensing and Milestone Payments
TypeLicensing Royalties
Description

Can-Fite generates revenue through upfront payments, regulatory and sales milestone payments, and royalties from licensing agreements with regional pharmaceutical partners for its drug candidates.

globenewswire.com
2Product Revenue
TypeLicensing Royalties
Description

The company reported $0.41 million in revenue for 2025 (down 40% year-over-year), derived from licensing agreements and recognition of upfront payments.

biospace.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels7 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Operations, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Can-Fite BioPharma is a clinical-stage biopharmaceutical company developing proprietary small molecule drug candidates that target the A3 adenosine receptor (A3AR) for oncology, inflammatory, and metabolic diseases. Its lead candidates include Piclidenoson (Phase III for plaque psoriasis), Namodenoson (Phase III for hepatocellular carcinoma, Phase IIb for MASH, Phase IIa for pancreatic cancer), CF602 for erectile dysfunction, and a preclinical Cannabinoids program. The company monetizes these assets by out-licensing them to regional pharmaceutical partners for development and commercialization.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 9-year cancer-free survival in hepatocellular carcinoma patient treated with Namodenoson
+4 more records
Product overview1 text field

Can-Fite BioPharma is an Israeli biopharmaceutical company with a platform technology utilizing the Gi protein associated A3 adenosine receptor (A3AR) as a therapeutic target. The company has an advanced clinical-stage pipeline of proprietary small molecule drug candidates addressing oncology, inflammatory, and metabolic diseases. The portfolio includes Piclidenoson (CF101) for psoriasis, Namodenoson (CF102) for liver cancer/HCC and metabolic diseases, CF602 for erectile dysfunction, and Cannabinoids in preclinical development. The compounds bind with nM affinity to A3AR and initiate de-regulation of NF-kB and Wnt signal transduction pathways resulting in anti-inflammatory and anti-cancer effects. Drugs have demonstrated excellent safety profiles with experience in over 1,600 patients in clinical studies.

Product and service1 record
1Piclidenoson (CF101)
Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2021-01-01
Description

Swiss company Ewopharma AG holds exclusive distribution rights for Namodenoson in Central Eastern European countries for liver cancer, NASH, and pancreatic cancer indications. Agreement includes upfront payment of US$2.25 million with up to US$40.45 million in milestones plus 17.5% royalties on net sales.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

CMS holds exclusive license for Namodenoson for the treatment of liver cancer and NASH in China, Taiwan, Hong Kong and Macao territories.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

CKD Pharmaceutical in South Korea holds exclusive license for Namodenoson for liver cancer and NASH treatment in the Korean market.

Strategic tierRegionalTypeChannel Partner/ Reseller/ Distributor
Description

Cipher Pharmaceuticals holds exclusive license for Piclidenoson for the treatment of psoriasis in Canada.

Strategic tierRegionalTypeChannel Partner/ Reseller/ Distributor
Description

Gebro Pharma GmbH holds exclusive license for Piclidenoson for the treatment of psoriasis in Switzerland, Spain, and Austria.

Strategic tierRegionalTypeChannel Partner/ Reseller/ Distributor
Description

Kyongbo Pharm holds exclusive license for Piclidenoson for the treatment of psoriasis in Korea.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Vetbiolix holds exclusive worldwide license to develop Piclidenoson for veterinary indications including canine osteoarthritis. The agreement is potentially worth up to $325 million in upfront, milestone, and royalty payments. Phase 2 clinical study completed enrollment with 118 dogs in Q3 2026.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight2 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Pioneer in NASH/MASH with obeticholic acid; acquired by Alfasigma. Provides relevant precedent for the regulatory and commercial challenges facing small-cap MASH developers and informs expectations for Can-Fite's MASH program.

TypeDirect peer
Description

Clinical-stage immunology company developing innovative inflammation treatments including IL-36R antagonist for psoriasis. Comparable size and development-stage profile to Can-Fite, with overlapping psoriasis therapeutic focus.

TypeEmerging player
Description

Clinical-stage developer of galectin-3 inhibitors for NASH cirrhosis and cancer immunotherapy. Similar small-cap clinical profile with liver fibrosis and oncology pipeline overlap with Namodenoson's HCC indication.

TypeDirect peer
Description

Clinical-stage biopharma developing Aramchol for NASH/MASH and HCC. Similar profile as a small-cap Israeli biopharma with a single-asset focus in hepatic diseases, providing direct competitive context for Can-Fite's Namodenoson.

TypeDirect peer
Description

French biopharma with elafibranor (Iqirvo, approved for PBC) and ongoing MASH development. Direct MASH peer with comparable clinical-stage profile and similar out-licensing strategy in select geographies.

TypeDirect peer
Description

Dermatology-focused biopharma with FDA-approved Zoryve for psoriasis. Direct competitor in plaque psoriasis with a similar small-cap, focused-therapeutic-area profile to Can-Fite's Piclidenoson.

TypeEmerging player
Description

Pre-acquisition clinical-stage biopharma developing seladelpar for PBC and MASH; acquired by Gilead in 2024 for $4.3B. Provides relevant precedent for valuation outcomes when late-stage MASH assets demonstrate clinical success.

TypeBroad incumbent
Description

Major pharmaceutical company with Sotyktu (deucravacitinib), an oral TYK2 inhibitor approved for psoriasis. Represents the dominant competitive threat to Piclidenoson in moderate-to-severe plaque psoriasis.

TypeDirect peer
Description

Direct competitor in MASH/NASH with approved drug Rezdiffra (resmetirom). Both companies target liver/metabolic disease with small-molecule approaches, making Madrigal the most direct read-across for Namodenoson's MASH Phase IIb program.

TypeBroad incumbent
Description

Established oncology player with Cabometyx (cabozantinib) approved for HCC. Sets the competitive benchmark for second-line HCC treatment that Namodenoson's Phase III must differentiate against.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds17 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors5 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

CanFite BioPharma

Clinical-Stage Biopharmaceuticalscanfite.com

Can-Fite BioPharma is an Israeli clinical-stage biopharmaceutical company that develops orally bioavailable small molecule A3 adenosine receptor (A3AR) agonists for oncology (liver and pancreatic cancer), inflammatory diseases (psoriasis), and metabolic disorders (MASH, obesity), generating revenue through regional out-licensing partnerships rather than direct commercialization.

What CanFite BioPharma does

Can-Fite BioPharma Ltd. is an Israeli clinical-stage biopharmaceutical company founded in 1994 and listed on NYSE American and the Tel Aviv Stock Exchange (ticker: CANF). The company develops orally bioavailable small molecule agonists targeting the Gi protein-associated A3 adenosine receptor (A3AR), a receptor that is highly expressed in inflammatory, cancer, and other pathological cells but minimally expressed in healthy cells. Compounds bind with nanomolar affinity to A3AR and modulate the NF-kB and Wnt signal transduction pathways to deliver anti-inflammatory and anti-cancer effects, with safety data accumulated across more than 1,600 patients in clinical studies.

The clinical pipeline comprises three core candidates and one preclinical program. Piclidenoson (CF101) is an A3AR agonist in pivotal Phase III for moderate-to-severe plaque psoriasis following positive Phase III COMFORT-1 topline data. Namodenoson (CF102) is the lead oncology asset, in pivotal Phase III for advanced hepatocellular carcinoma, Phase IIb for MASH, and Phase IIa for pancreatic cancer; it has received FDA Orphan Drug Designation for HCC and pancreatic cancer plus FDA Fast Track Designation for second-line HCC. CF602 is an A3AR allosteric modulator in preclinical development for erectile dysfunction, particularly for diabetic patients and PDE5 non-responders, and a cannabinoid program targets the endocannabinoid system. The company pursues a pure out-licensing model, granting exclusive regional development and commercialization rights to specialized pharmaceutical distributors in exchange for upfront payments, regulatory and sales milestones, and royalties on net sales.

Can-Fite generates revenue from licensing agreements rather than direct product sales. Current commercial partners include Ewopharma (Central Eastern Europe), CMS (China/Hong Kong/Macao/Taiwan), Chong Kun Dang (South Korea), Cipher Pharmaceuticals (Canada), Gebro Pharma (Switzerland/Spain/Austria), Kyongbo Pharm (South Korea), and Vetbiolix (worldwide veterinary). The Ewopharma agreement alone includes a $2.25 million upfront payment, up to $40.45 million in milestones, and 17.5% royalties on net sales; the Vetbiolix veterinary deal is potentially worth up to $325 million. FY2025 revenue was $0.41 million against a $9.83 million net loss, with operations funded by recurring equity raises totaling approximately $19 million between November 2023 and March 2026, led by H.C. Wainwright & Co.

CanFite BioPharma firmographics

Firmographics
Name
CanFite BioPharma
Legal name
Can-Fite BioPharma Ltd.
Website
https://canfite.com
Company type
Public
Founded year
1994
Operating status
Operating
Headcount range
1–10 employees
Short description
Can-Fite BioPharma is an Israeli clinical-stage biopharmaceutical company that develops orally bioavailable small molecule A3 adenosine receptor (A3AR) agonists for oncology (liver and pancreatic cancer), inflammatory diseases (psoriasis), and metabolic disorders (MASH, obesity), generating revenue through regional out-licensing partnerships rather than direct commercialization.
Ownership category
akta.pro rank

Where CanFite BioPharma is headquartered

Location

Headquarters

HQ city
Petah Tiqva
HQ country
Israel
HQ region
Middle East

Offices2 records

Markets served

CanFite BioPharma business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Others

Revenue model

  1. Licensing and Milestone Payments: Can-Fite generates revenue through upfront payments, regulatory and sales milestone payments, and royalties from licensing agreements with regional pharmaceutical partners for its drug candidates.
  2. Product Revenue: The company reported $0.41 million in revenue for 2025 (down 40% year-over-year), derived from licensing agreements and recognition of upfront payments.

Go-to-market motion1 record

Distribution channels7 records

Marketing channels4 records

CanFite BioPharma product offering

Product offering

Core offering

Can-Fite BioPharma is a clinical-stage biopharmaceutical company developing proprietary small molecule drug candidates that target the A3 adenosine receptor (A3AR) for oncology, inflammatory, and metabolic diseases. Its lead candidates include Piclidenoson (Phase III for plaque psoriasis), Namodenoson (Phase III for hepatocellular carcinoma, Phase IIb for MASH, Phase IIa for pancreatic cancer), CF602 for erectile dysfunction, and a preclinical Cannabinoids program. The company monetizes these assets by out-licensing them to regional pharmaceutical partners for development and commercialization.

Product overview

Can-Fite BioPharma is an Israeli biopharmaceutical company with a platform technology utilizing the Gi protein associated A3 adenosine receptor (A3AR) as a therapeutic target. The company has an advanced clinical-stage pipeline of proprietary small molecule drug candidates addressing oncology, inflammatory, and metabolic diseases. The portfolio includes Piclidenoson (CF101) for psoriasis, Namodenoson (CF102) for liver cancer/HCC and metabolic diseases, CF602 for erectile dysfunction, and Cannabinoids in preclinical development. The compounds bind with nM affinity to A3AR and initiate de-regulation of NF-kB and Wnt signal transduction pathways resulting in anti-inflammatory and anti-cancer effects. Drugs have demonstrated excellent safety profiles with experience in over 1,600 patients in clinical studies.

Differentiator

Problem solved

Functional benefit

Products and services

  • Piclidenoson (CF101)

Quantifiable outcome

  • 9-year cancer-free survival in hepatocellular carcinoma patient treated with Namodenoson
  • +4 more outcomes

Companies that use CanFite BioPharma

Customer profile

Segments3 records

Ideal customer profiles1 record

CanFite BioPharma technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

CanFite BioPharma partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and regional.

  • Ewopharma AGcoreChannel Partner/ Reseller/ Distributor · 1 January 2021Swiss company Ewopharma AG holds exclusive distribution rights for Namodenoson in Central Eastern European countries for liver cancer, NASH, and pancreatic cancer indications. Agreement includes upfront payment of US$2.25 million with up to US$40.45 million in milestones plus 17.5% royalties on net sales.
  • CMS (China Medical System)coreChannel Partner/ Reseller/ DistributorCMS holds exclusive license for Namodenoson for the treatment of liver cancer and NASH in China, Taiwan, Hong Kong and Macao territories.
  • Chong Kun Dang (CKD) PharmaceuticalcoreChannel Partner/ Reseller/ DistributorCKD Pharmaceutical in South Korea holds exclusive license for Namodenoson for liver cancer and NASH treatment in the Korean market.
  • Cipher PharmaceuticalsregionalChannel Partner/ Reseller/ DistributorCipher Pharmaceuticals holds exclusive license for Piclidenoson for the treatment of psoriasis in Canada.
  • Gebro Pharma GmbHregionalChannel Partner/ Reseller/ DistributorGebro Pharma GmbH holds exclusive license for Piclidenoson for the treatment of psoriasis in Switzerland, Spain, and Austria.
  • Kyongbo PharmregionalChannel Partner/ Reseller/ DistributorKyongbo Pharm holds exclusive license for Piclidenoson for the treatment of psoriasis in Korea.
  • VetbiolixcoreChannel Partner/ Reseller/ DistributorVetbiolix holds exclusive worldwide license to develop Piclidenoson for veterinary indications including canine osteoarthritis. The agreement is potentially worth up to $325 million in upfront, milestone, and royalty payments. Phase 2 clinical study completed enrollment with 118 dogs in Q3 2026.

Scale indicators8 records

Recent moves7 records

Expansion highlights2 records

CanFite BioPharma competitors and assessment

Company assessment

Broad incumbents

  • Intercept Pharmaceuticals: Pioneer in NASH/MASH with obeticholic acid; acquired by Alfasigma. Provides relevant precedent for the regulatory and commercial challenges facing small-cap MASH developers and informs expectations for Can-Fite's MASH program.
  • Bristol-Myers Squibb: Major pharmaceutical company with Sotyktu (deucravacitinib), an oral TYK2 inhibitor approved for psoriasis. Represents the dominant competitive threat to Piclidenoson in moderate-to-severe plaque psoriasis.
  • Exelixis: Established oncology player with Cabometyx (cabozantinib) approved for HCC. Sets the competitive benchmark for second-line HCC treatment that Namodenoson's Phase III must differentiate against.

Direct peers

  • AnaptysBio: Clinical-stage immunology company developing innovative inflammation treatments including IL-36R antagonist for psoriasis. Comparable size and development-stage profile to Can-Fite, with overlapping psoriasis therapeutic focus.
  • Galmed Pharmaceuticals: Clinical-stage biopharma developing Aramchol for NASH/MASH and HCC. Similar profile as a small-cap Israeli biopharma with a single-asset focus in hepatic diseases, providing direct competitive context for Can-Fite's Namodenoson.
  • Genfit: French biopharma with elafibranor (Iqirvo, approved for PBC) and ongoing MASH development. Direct MASH peer with comparable clinical-stage profile and similar out-licensing strategy in select geographies.
  • Arcutis Biotherapeutics: Dermatology-focused biopharma with FDA-approved Zoryve for psoriasis. Direct competitor in plaque psoriasis with a similar small-cap, focused-therapeutic-area profile to Can-Fite's Piclidenoson.
  • Madrigal Pharmaceuticals: Direct competitor in MASH/NASH with approved drug Rezdiffra (resmetirom). Both companies target liver/metabolic disease with small-molecule approaches, making Madrigal the most direct read-across for Namodenoson's MASH Phase IIb program.

Emerging players

  • Galectin Therapeutics: Clinical-stage developer of galectin-3 inhibitors for NASH cirrhosis and cancer immunotherapy. Similar small-cap clinical profile with liver fibrosis and oncology pipeline overlap with Namodenoson's HCC indication.
  • CymaBay Therapeutics: Pre-acquisition clinical-stage biopharma developing seladelpar for PBC and MASH; acquired by Gilead in 2024 for $4.3B. Provides relevant precedent for valuation outcomes when late-stage MASH assets demonstrate clinical success.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

CanFite BioPharma social profiles

Digital presence

CanFite BioPharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

CanFite BioPharma leadership team

Management profile

Number of profiles

Profiles7 records

CanFite BioPharma subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

CanFite BioPharma funding detail

Funding detail

Funding overview

Funding rounds17 records

Investors5 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

CanFite BioPharma M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about CanFite BioPharma

What does CanFite BioPharma do?

Can-Fite BioPharma is a clinical-stage biopharmaceutical company developing proprietary small molecule drug candidates that target the A3 adenosine receptor (A3AR) for oncology, inflammatory, and metabolic diseases. Its lead candidates include Piclidenoson (Phase III for plaque psoriasis), Namodenoson (Phase III for hepatocellular carcinoma, Phase IIb for MASH, Phase IIa for pancreatic cancer), CF602 for erectile dysfunction, and a preclinical Cannabinoids program. The company monetizes these assets by out-licensing them to regional pharmaceutical partners for development and commercialization.

Is CanFite BioPharma a public or private company?

CanFite BioPharma is a public company. It is classified as public and is currently operating.

When was CanFite BioPharma founded?

CanFite BioPharma was founded in 1994. It employs 1 to 10 people.

Where is CanFite BioPharma based?

CanFite BioPharma is headquartered in Petah Tiqva, Israel, in the Middle East region.

How does CanFite BioPharma make money?

Two revenue lines are on record. Licensing and Milestone Payments are the primary driver. The others are product Revenue.

Who are CanFite BioPharma's main competitors?

Broad incumbents on record are Intercept Pharmaceuticals, Bristol-Myers Squibb and Exelixis. Direct peers are AnaptysBio, Galmed Pharmaceuticals, Genfit, Arcutis Biotherapeutics and Madrigal Pharmaceuticals. Emerging players are Galectin Therapeutics and CymaBay Therapeutics.

Does CanFite BioPharma have an API?

No public API is recorded for CanFite BioPharma.

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Live signals
AInvestCANF Delivered a Headline Win on September 2—Then Fell. The Only Level That Matters Is the Q4 ReadoutCan-Fite reported prolonged survival in its Phase III liver-cancer trial, but blinded pooled data across both arms offers no conclusive efficacy evidence. Shares fell 5% to $2.23 by September 8, with $6.45M cash reserves facing pressure from multiple Phase III programs. The Q4 2026 interim analysis will provide the first definitive comparison of Namodenoson versus placebo.Benzinga12 Health Care Stocks Moving In Wednesday's Pre-Market Session - Can Fite Biopharma (AMEX:CANF), Aligos THealthcare stocks showed mixed pre-market moves on Wednesday, with Fite Biopharma rising 20.4% to $3.96 and Aligos Therapeutics up 18.39% to $7.21. Losers included CDT Equity, which fell 23.6% to $1.13, and Jasper Therapeutics, down 18.67% to $0.57.BioSpaceCan-Fite: Namodenoson Enhances the Anti-Cancer Effect of Chemotherapy in Pancreatic CancerCan-Fite announced preclinical findings that namodenoson enhances gemcitabine's anti-cancer effect in pancreatic cancer, increasing cleaved caspase-3 levels. The results support its planned Phase IIb study combining namodenoson with gemcitabine and nab-paclitaxel in advanced pancreatic adenocarcinoma.BioSpaceCan-Fite Highlights Advanced FDA and EMA Regulatory Status of its Phase III Drug CandidatesCan-Fite BioPharma updated its Phase III programs for Namodenoson and Piclidenoson, with Namodenoson in a pivotal HCC study and Piclidenoson in psoriasis. Namodenoson holds FDA Fast Track and U.S./EU Orphan Drug designations, while Piclidenoson advances in psoriasis. The company expects these regulatory pathways to support potential marketing authorization applications.GlobeNewswireCan-Fite Launches First Clinical Program for Piclidenoson in the Rare Genetic Disease Lowe SyndromeCan-Fite BioPharma submitted a Phase 2 clinical study protocol for Piclidenoson in Lowe syndrome, a rare genetic disorder with no approved therapies. The open-label, single-center trial will evaluate the drug in 5 adult patients over six months, with renal uptake as the primary endpoint. The company aims to use results for regulatory discussions and potential registration.Quiver QuantitativeCan-Fite BioPharma Announces ESMO 2026 Poster Presentation of Positive Phase 2a Namodenoson Data in Advanced Pancreatic Cancer | Quiver QuantitativeCan-Fite BioPharma Ltd. announced that positive results from its Phase 2a study of Namodenoson in advanced pancreatic ductal adenocarcinoma have been accepted for poster presentation at the ESMO Congress 2026. The study demonstrated durable disease stabilization and encouraging survival outcomes in patients who had progressed following prior standard therapies, including one patient remaining alive more than 18 months after receiving Namodenoson as a second-line treatment. Can-Fite is now planning a Phase 2b study to evaluate Namodenoson in combination with chemotherapy based on these findings.Investing.comCan-Fite’s pancreatic cancer study accepted for ESMO presentation By Investing.comCan-Fite BioPharma announced that an abstract from its Phase 2a study of Namodenoson in advanced pancreatic ductal adenocarcinoma has been accepted for poster presentation at the European Society for Medical Oncology Congress 2026. The study achieved its primary safety endpoint and demonstrated disease stabilization and survival outcomes in patients who had progressed on standard therapies, with the company planning a Phase 2b study evaluating Namodenoson in combination with chemotherapy. H.C. Wainwright subsequently raised its price target for Can-Fite to $8.00 from $5.00 while maintaining a Buy rating.Investing.comCan-Fite’s pancreatic cancer study accepted for ESMO presentation By Investing.comCan-Fite BioPharma Ltd. announced that its Phase 2a study abstract of Namodenoson in advanced pancreatic ductal adenocarcinoma has been accepted for poster presentation at the European Society for Medical Oncology Congress 2026. The study achieved its primary safety endpoint and demonstrated disease stabilization with survival outcomes in patients who had progressed following standard therapies. The company is planning a Phase 2b study to evaluate Namodenoson in combination with chemotherapy for pancreatic cancer.GlobeNewswireCan-Fite Positive Phase 2a Pancreatic Cancer Study Data Accepted for Presentation at ESMO Congress 2026, One of the World's Premier Scientific Meetings in OncologyCan-Fite BioPharma announced that an abstract presenting positive Phase 2a study results for Namodenoson in advanced pancreatic ductal adenocarcinoma has been accepted for poster presentation at the ESMO Congress 2026. The Phase 2a study achieved its primary safety endpoint and demonstrated encouraging survival outcomes with durable disease stabilization in patients who had progressed following prior standard therapies. The company is now planning a Phase 2b study to evaluate Namodenoson in combination with chemotherapy based on these encouraging clinical findings and supportive preclinical evidence.Stock TitanCan-Fite Phase 2a Pancreatic Data Accepted at ESMO 2026Can-Fite BioPharma announced that positive results from its Phase 2a study of Namodenoson in advanced pancreatic cancer patients have been accepted for poster presentation at the ESMO Congress 2026. The study achieved its primary safety endpoint and demonstrated encouraging survival outcomes with durable disease stabilization in patients who had progressed following prior standard therapies, including one second-line patient remaining alive more than 18 months. Can-Fite is now planning to advance to a Phase 2b study evaluating Namodenoson in combination with chemotherapy based on these encouraging findings and supportive preclinical evidence.