Can-Fite H1FY26 Results: Net loss narrows 5.5% to $4.6 million
- Net loss narrowed 5.5% YoY to $4.60 million for H1 2026
- Revenue remained flat at $0.20 million from out-licensing advances
- R&D expenses rose 13.9% to $3.45 million due to trial acceleration
- Blinded survival data in Phase III liver cancer study exceeds expectations
- Cash position decreased to $7.03 million amid operating losses

*this image is generated using AI for illustrative purposes only.
Can-Fite BioPharma Ltd. (NYSE: CANF) reported a net loss of $4.60 million for the six months ended June 30, 2026, compared to a loss of $4.87 million in the same period last year. The biotechnology firm also announced that blinded overall survival data in its pivotal Phase III liver cancer study appears longer than anticipated.
The company generated revenues of $0.20 million, unchanged from H1 2025, derived from advance payments under existing out-licensing agreements. Research and development expenses rose 13.86% to $3.45 million, driven by acceleration in its Namodenoson and Piclidenoson programs. General and administrative expenses fell 31.40% to $1.42 million, primarily due to lower investor relations costs.
Clinical Progress
Can-Fite provided updates on three key therapeutic areas:
- Hepatocellular Carcinoma: Blinded overall survival in the ongoing pivotal Phase III study of Namodenoson appears longer than originally anticipated. The company is evaluating an earlier timing for the planned interim analysis.
- Pancreatic Cancer: A Phase 2a study of Namodenoson achieved its primary safety endpoint and demonstrated durable overall survival outcomes in heavily pretreated patients. An abstract has been accepted for presentation at the ESMO Congress 2026.
- Psoriasis: Enrolment of the first 247 patients in the pivotal Phase 3 study of Piclidenoson is complete. The study has reached the pre-specified interim analysis stage, with results expected in Q1 2027.
Financial Performance
| Metric | H1 2026 | H1 2025 | Change |
|---|---|---|---|
| Revenue | $0.20 million | $0.20 million | 0% |
| R&D Expenses | $3.45 million | $3.03 million | +13.86% |
| G&A Expenses | $1.42 million | $2.07 million | -31.40% |
| Net Loss | $4.60 million | $4.87 million | -5.54% |
Net financial income increased to $0.08 million from $0.02 million in the prior year, mainly due to higher interest income from bank deposits. Cash and cash equivalents stood at $7.03 million as of June 30, 2026, down from $8.53 million at year-end 2025. The decrease was primarily due to operating losses, partially offset by proceeds from share and warrant issuances.
What the Numbers Show
The narrowing of the net loss was driven entirely by operational cost control rather than revenue growth or R&D efficiency. While R&D spending accelerated by $0.42 million to support late-stage trials, G&A expenses contracted by $0.65 million. This divergence indicates that the improvement in the bottom line resulted from reduced administrative overhead, specifically investor relations costs, rather than a reduction in clinical development burn rate.
How might the potential acceleration of the interim analysis in the Namodenoson Phase III liver cancer study impact Can-Fite's timeline for regulatory submissions and commercialization?
Given the cash balance of $7.03 million and ongoing R&D burn, what are the specific milestones or financing events required to ensure operational runway through the expected Q1 2027 Piclidenoson data readout?
What strategic implications could the accepted abstract at ESMO Congress 2026 have for partnership discussions or licensing deals regarding Namodenoson in pancreatic cancer?

































