Can-Fite highlights regulatory status of Phase III drug candidates
Namodenoson holds FDA Fast Track and orphan drug designations for liver cancer in the U.S. and Europe; Piclidenoson is also in Phase III for psoriasis.
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Biopharmaceutical developer of oral treatments for cancer, inflammatory, metabolic diseases
canfite.comLast updated
In short: Can-Fite advanced its clinical pipeline, highlighted by positive pancreatic cancer data for Namodenoson and Phase 3 psoriasis progress.
Namodenoson holds FDA Fast Track and orphan drug designations for liver cancer in the U.S. and Europe; Piclidenoson is also in Phase III for psoriasis.
Phase 2 study protocol submitted to Bambino Gesù Children's Hospital; aims to evaluate efficacy and safety in five adult patients.
The Phase 2a study of Namodenoson met its primary safety endpoint and showed encouraging survival outcomes.
The interim analysis follows an FDA- and EMA-agreed protocol, with results expected in Q4 2026 or Q1 2027.
Fite’s Ongoing Phase IIb Study Design Following Positive Phase IIa Results Ramat Gan, Israel, Aug. 17, 2026 (GLOBE NEWSWIRE) ...
Detailed price information for Can-Fite Biopharma Ltd ADR (CANF-A) from The Globe and Mail including charting and trades.
Detailed price information for Can-Fite Biopharma Ltd ADR (CANF-A) from The Globe and Mail including charting and trades.
Interim analysis to be conducted under an FDA- and EMA-agreed protocol Ramat Gan, Israel, July 06, 2026 (GLOBE NEWSWIRE) -- Can-Fite BioPharma Ltd. (NYSE American...
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