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Namodenoson in the Treatment of Non-Alcoholic Steatohepatitis (NASH)

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NCT04697810

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

Phase
Phase 2
Status
Unknown status
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
114estimated
Sites
24
Countries
Bosnia and Herzegovina, Bulgaria, Israel +3

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
Start2021-12-10actualWhen the study began enrolling
Primary completion2025-04-15estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-10-15estimatedThe whole study's end, after follow-up
First posted2021-01-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-07-31actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • NASH - Nonalcoholic Steatohepatitis

Interventions

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

Primary outcomes

what the primary-completion date above is the date OF
Non-Alcoholic Fatty Liver Disease (NAFLD) activity score (NAS)
measured 36 weeks
Adverse events (AEs)
measured 36 weeks

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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