Stock Markets April 30, 2026 08:51 AM

Can-Fite Shares Surge After Positive Phase 2a Results for Namodenoson in Advanced Pancreatic Cancer

Early trial data show durable disease stabilization and an encouraging safety profile, with full efficacy readouts expected in coming months

By Derek Hwang CANF
Can-Fite Shares Surge After Positive Phase 2a Results for Namodenoson in Advanced Pancreatic Cancer
CANF

Can-Fite BioPharma's stock climbed after the company disclosed positive Phase 2a data for namodenoson in patients with advanced pancreatic cancer. The fully enrolled study reported preliminary signs of clinical activity, including durable disease stabilization in a heavily pretreated population, a favorable safety profile, and several patients remaining on treatment for extended periods. Top-line efficacy results are due in the coming months and will be presented at a clinical conference.

Key Points

  • Can-Fite shares rose 18% after the company reported positive Phase 2a data for namodenoson in advanced pancreatic cancer - impacting biotech and healthcare equities.
  • The fully enrolled study showed preliminary clinical activity, with stable disease in over 30% of evaluable patients and one patient receiving treatment beyond 16 months - relevant to oncology drug development assessments.
  • Namodenoson demonstrated a safety and tolerability profile consistent with prior reports; 35% of patients remain on therapy and in follow up.

Shares of Can-Fite BioPharma Ltd. rallied after the biotechnology company announced positive Phase 2a findings for namodenoson in patients with advanced pancreatic cancer. The stock rose 18% on the trading session following the disclosure.

Can-Fite described the trial as fully enrolled and said the preliminary data provide evidence of clinical activity in a population that had received extensive prior therapy. A key signal from the study was durable disease stabilization observed among patients assessed for response.

The company reported that stable disease was documented in more than 30% of evaluable patients. Several individuals experienced prolonged durations on therapy, including one patient who remained on treatment beyond 16 months. Can-Fite also stated that 35% of participants continue to receive the drug and are in follow-up at this time.

In addition to disease control signals, namodenoson displayed a favorable safety and tolerability profile in this trial, consistent with the company’s earlier reports.

Commenting on the results, Pnina Fishman, Can-Fite’s Chairperson and Chief Scientific Officer, said: "As we continue to analyse the data, we are encouraged by the emerging signal of durable disease stabilization observed in this study." She added: "Importantly, a meaningful proportion of patients remain on therapy for extended periods, supporting the continued clinical development of namodenoson in pancreatic cancer."

Can-Fite noted that full efficacy analyses are pending. These will include top-line results for progression-free survival and overall survival, which the company expects to report in the coming months. The firm intends to present those results at a clinical conference once available.

Can-Fite develops a portfolio of proprietary small molecule therapies aimed at treating cancer and inflammatory diseases. The Phase 2a update on namodenoson adds to the company’s clinical-stage programing and offers an early signal for further study in pancreatic cancer.


Context for investors and markets

  • The stock reaction reflects investor attention to early clinical readouts in oncology programs.
  • Final efficacy metrics to be released in the coming months will be key to assessing broader commercial and clinical potential.

Risks

  • The data reported are preliminary from a Phase 2a study; full efficacy analyses including progression-free survival and overall survival are still pending and will determine the strength of the clinical signal.
  • The trial population was heavily pretreated, which can complicate interpretation of outcomes and may limit generalizability of results across broader patient groups.
  • Market reaction is tied to early-stage results; subsequent top-line efficacy data or conference presentation could lead to volatility in the company’s stock and affect investor sentiment in the biotech sector.

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