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CANFNYSE

Can-Fite BioPharma Ltd.

Biopharma developer (SEC filing verified)·Phase 3·Ramat Gan, Israel·CEO: Mr. Motti Farbstein
OncologyImmunology

CANF evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

What matters most for CANF—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · CANF

Can-Fite BioPharma Ltd. is an advanced clinical-stage biotechnology company developing small molecule orally bioavailable drugs for inflammatory, oncology, and liver diseases, with lead candidates piclidenoson and namodenoson in Phase 2/3 trials and no approved products or commercial sales to date.

Key risk: History of losses and need for capital

5.8/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$7.3M

Cash Runway

2.2 mo

Lead Asset

Financial data as of Dec 31, 2025.

Tracking 2 clinical trials · 3 catalysts for Can-Fite BioPharma Ltd..

AI OverviewAI overview is shown in English only.

Can-Fite BioPharma Ltd. is an advanced clinical-stage biotechnology company developing small molecule orally bioavailable drugs for inflammatory, oncology, and liver diseases, with lead candidates piclidenoson and namodenoson in Phase 2/3 trials and no approved products or commercial sales to date.

  • Cash and cash equivalents of $5.5 million and short-term deposits of $3.0 million as of December 31, 2025 [sec · filed 2026-03-26].
  • Accumulated deficit of approximately $176.2 million as of December 31, 2025 [sec · filed 2026-03-26].
  • Total revenue of $0.4 million for the year ended December 31, 2025, primarily from out-licensing agreements [sec · filed 2026-03-26].
  • Lead product candidates: piclidenoson (Phase 3 COMFORT study in psoriasis) and namodenoson (Phase 2 LIVERATION study in hepatocellular carcinoma) [sec · filed 2026-03-26].
  • No product candidates have been approved for sale or marketing, and there have been no commercial sales to date [sec · filed 2026-03-26].

What works

  • The company has advanced multiple product candidates into clinical development, including a Phase 3 study for piclidenoson in psoriasis and a Phase 2 study for namodenoson in HCC [sec · filed 2026-03-26].
  • Can-Fite's strategy focuses on small molecule orally bioavailable drugs, which may offer advantages in patient convenience and manufacturing efficiency [sec · filed 2026-03-26].
  • Existing out-licensing agreements with partners such as Cipher, CKD, Gebro, and Ewopharma provide a source of revenue and validation of the company's technology [sec · filed 2026-03-26].
  • The company has sufficient cash resources to meet its requirements for the next twelve months from the date of its Annual Report [sec · filed 2026-03-26].

What to weigh

  • Can-Fite has incurred operating losses since inception and expects to continue incurring substantial losses for the foreseeable future, with an accumulated deficit of $176.2 million as of December 31, 2025 [sec · filed 2026-03-26].
  • The company will need to raise additional capital to meet future business requirements, which may be costly or difficult to obtain and would dilute current shareholders [sec · filed 2026-03-26].
  • None of the company's product candidates have been approved for sale or marketing, and there is no guarantee that clinical trials will be successful or lead to regulatory approval [sec · filed 2026-03-26].
  • The company may not currently satisfy NYSE American continued listing requirements, and delisting could occur if requirements are not met [sec · filed 2026-03-26].

From the filings

Quoted directly from source documents.

  • Cash position and accumulated deficit as of December 31, 2025

    As of December 31, 2025, we had cash and cash equivalents of $5.5 million and short-term deposits of $3.0 million.

    SEC filings · March 26, 2026

  • Accumulated deficit

    As of December 31, 2025, we had an accumulated deficit of approximately $176.2 million.

    SEC filings · March 26, 2026

  • No approved products or commercial sales

    None of our product candidates have been approved for sale or marketing and, to date, there have been no commercial sales of any of our product candidates.

    SEC filings · March 26, 2026

  • Need for additional capital

    We will need to raise additional capital to meet our business requirements in the future, and such capital raising may be costly or difficult to obtain and will dilute current shareholders' ownership interests.

    SEC filings · March 26, 2026

Catalyst timeline

  • 2026-09-30 · Phase2_Topline · namodenoson — Phase 2 Readout: namodenosonTopline data from the Phase 2 study of namodenoson in hepatocellular carcinoma will be reported.
  • 2026-09-30 · Phase2_Topline · piclidenoson — Phase 2 Readout: piclidenosonTopline data from the Phase 2 study of piclidenoson will be reported.
  • 2028-06-01 · Phase3_Topline — Phase 3 Topline: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Daily PiTopline data from the Phase 3 study of piclidenoson in psoriasis are expected.
Risks & what to watch (4)

Key risks

  • History of losses and need for capitalOperating losses since inception; accumulated deficit of $176.2M; will need additional capital which may be costly or dilutive [sec · filed 2026-03-26].
  • No approved products or commercial salesNone of the product candidates have been approved for sale or marketing; no commercial sales to date [sec · filed 2026-03-26].
  • Clinical and regulatory uncertaintyMost product candidates never complete clinical development; no guarantee of regulatory approval for any candidate [sec · filed 2026-03-26].
  • Potential NYSE American delistingCompany may not currently satisfy NYSE American continued listing requirements; delisting could occur [sec · filed 2026-03-26].

What to watch

  • Interim analysis data from the Phase 3 COMFORT study of piclidenoson in psoriasis, expected in Q2 2027 [sec · filed 2026-03-26].
  • Submission of the study protocol for Lowe syndrome to regulators, expected in Q2 2026 [sec · filed 2026-03-26].
  • Topline data from the Phase 2 study of namodenoson in HCC, expected by September 30, 2026 [upcoming catalysts].
  • Topline data from the Phase 2 study of piclidenoson, expected by September 30, 2026 [upcoming catalysts].

Sources: SEC filings · Generated August 26, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash Runway0.6

2.2 months

Financial Health8.9

D/E 0.70 · 0% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum8.0

3 upcoming, next in ~31d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

12

Total value held

$322K

Showing top 10 of 12 institutional holders of Can-Fite BioPharma Ltd.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
1.1%
Days to cover
0.0
Shares short
23,418
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

CANF short interest

Frequently asked questions

What is the AI investment thesis for Can-Fite BioPharma Ltd.?

Can-Fite BioPharma Ltd. is an advanced clinical-stage biotechnology company developing small molecule orally bioavailable drugs for inflammatory, oncology, and liver diseases, with lead candidates piclidenoson and namodenoson in Phase 2/3 trials and no approved products or commercial sales to date.

What is Can-Fite BioPharma Ltd.'s next catalyst?

Can-Fite BioPharma Ltd.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: namodenoson" — expected September 30, 2026.

Who is the CEO of Can-Fite BioPharma Ltd.?

Mr. Motti Farbstein is the chief executive officer of Can-Fite BioPharma Ltd. (CANF).

Where is Can-Fite BioPharma Ltd. headquartered?

Can-Fite BioPharma Ltd. (CANF) is headquartered in Ramat Gan, Israel.

What therapeutic areas does Can-Fite BioPharma Ltd. focus on?

Can-Fite BioPharma Ltd. develops therapies across Oncology, Immunology.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.