TrialSignal
Clinical trial intelligence report
A Phase 2 Study in the Second-Line Treatment of Advanced Hepatocellular Carcinoma in Subjects With Child-Pugh Class B Cirrhosis
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT02128958-Jun 24, 2026
NCT ID
NCT02128958
Status
COMPLETED
Phase
Phase 2
Sponsor
Can-Fite BioPharma
Executive brief
Investment-Ready Snapshot
Can-Fite BioPharma's CF102 is positioned as a second-line treatment for advanced hepatocellular carcinoma (HCC) in patients with Child-Pugh Class B cirrhosis. The market for HCC therapies is expanding, driven by increasing incidence rates and the need for effective treatments in advanced stages. CF102's unique mechanism targeting A3AR may provide a competitive edge over existing therapies. However, the competitive landscape includes established players with approved therapies, necessitating a robust demonstration of efficacy and safety to secure market share. Diligence should focus on the trial's outcomes, potential regulatory pathways, and reimbursement scenarios.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02128958
Indication
Hepatocellular Carcinoma
Modality
small molecule
Target
Adenosine A3 receptor (A3AR)
Intervention
CF102, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.