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Namodenoson in the Treatment of Advanced Hepatocellular Carcinoma in Patients With Child-Pugh Class B7 Cirrhosis

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NCT05201404

Sponsored by Can-Fite BioPharma (industry) · CANF — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
471estimated
Sites
32
Countries
Bosnia and Herzegovina, Bulgaria, Israel +6

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-03-15actualWhen the study began enrolling
Primary completionFeb 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionOct 2026estimatedThe whole study's end, after follow-up
First posted2022-01-21actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-04-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Hepatocellular Carcinoma
  • Cirrhosis

Interventions

  • Drug: Namodenoson — also filed as CF102
  • Drug: Placebo — also filed as Inactive control

Primary outcome

what the primary-completion date above is the date OF
Overall Survival (OS)
measured From the time of randomization until the date of death from any cause, assessed up to 60 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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