Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Namodenoson in the Treatment of Advanced Hepatocellular Carcinoma in Patients With Child-Pugh Class B7 Cirrhosis
NCT05201404 · View on ClinicalTrials.gov ↗
Study Summary
This is a clinical trial in patients with advanced hepatocellular carcinoma (HCC) and Child-Pugh Class B7 (CPB7) cirrhosis whose disease has progressed on at least 1st-line therapy. The trial will evaluate the efficacy and safety of namodenoson as compared to placebo.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Namodenoson
Study Locations (20)
Other
- 841 University Clinical Centre of Republic of Srpska — Banja Luka
- 843 University Clinical Hospital Mostar — Mostar
- 842 University Clinical Centre Sarajevo — Sarajevo
- 831 Dept of Medical Oncology, Complex Oncology Ctr - Burgas EOOD — Burgas
- 835 First Department of Medical Oncology, Gastroenterology and Pulmology, Complex Oncology Center - Plovdiv EOOD, Plovdiv — Plovdiv
- Medical Center Leo Clinic EOOD Plovdiv — Plovdiv
- 834 Medical Oncology Dept, Univ Multiprofile Hospital for Active Treatment "Sv. Ivan Rilski" EAD, Sofia — Sofia
- 518 Rabin Medical Center Beilinson Hospital — Petah Tikva
- 872 IMSP Institute of Oncology — Chisinau
- Site 858 — Koszalin
- Site 852 — Krakow
- Site 857 — Mysłowice
- Site 859 — Przemyśl
- Site 855 — Warsaw
- Site 850 — Wroclaw
- 802 Institutul Regional de Gastroenterologie si Hepatologie — Cluj-Napoca
- 807 IOCN, Medical Oncology — Cluj-Napoca
- 809 Spitalul Clinic Judetean de Urgenta Constanta Oncology Dept — Constanța
- 801 Oncology Center "Sf. Nectarie" Medical Oncology — Craiova
Texas
- Site 881 — Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 471 participants |
| Start Date | 2023-03-15 |
| Est. Completion | 2026-10 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05201404
The ClinicalTrials.gov registry entry for NCT05201404 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 471 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Can-Fite BioPharma, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Hepatocellular Carcinoma appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05201404 reports 20 study locations spanning 2 distinct geographic areas — top geographies include Other, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05201404 about?
NCT05201404 is a clinical study titled "Namodenoson in the Treatment of Advanced Hepatocellular Carcinoma in Patients With Child-Pugh Class B7 Cirrhosis". This is a clinical trial in patients with advanced hepatocellular carcinoma (HCC) and Child-Pugh Class B7 (CPB7) cirrhosis whose disease has progressed on at least 1st-line therapy. The trial will evaluate the efficacy and safety of namodenoson as compared to placebo.
What is the current status of trial NCT05201404?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 471 participants. The study started on 2023-03-15. Estimated completion is 2026-10.
What conditions does trial NCT05201404 study?
This clinical trial studies the following conditions: Hepatocellular Carcinoma, Cirrhosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05201404?
The interventions under investigation include: Placebo (DRUG), Namodenoson (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05201404?
This trial is sponsored by Can-Fite BioPharma, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05201404 being conducted?
This trial has 20 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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