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A phase II study with Tegafur/Uracil and Peg-Interferon after TACE for hepatocelluler carcinoma

A phase II study with Tegafur/Uracil and Peg-Interferon after TACE for hepatocelluler carcinoma - A phase II study with Tegafur/Uracil and Peg-Interferon after TACE for hepatocelluler carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000275
Enrollment
20
Registered
2005-11-02
Start date
2005-10-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced hepatocellular carcinoma

Interventions

Combination chemotherapy with Peg-Interferon and oral Tegafur/Uracil

Sponsors

The third department of Internal Medicine, Wakayama Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically or clinically confirmed hepatocellular carcinoma 2)Measurable and hypervascular hepatocellular carcinoma on contrast CT 3)No indication or resistance hepatic resection and percutaneous treatment 4)No tumor thrombus in main portal vein 5)Child-Pugh score of A or B 6)Adequate bone marrow function 7)Ages 20years and above,under 80 years 8)Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 9)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Allergic reaction to IFN and/or UFT 2)Positive by prick test of IFN 3)Severe liver damage after TAE 4)Autoimmune disease 5)Depression or mental neuropathic illness 6)Uncontrolled heart or renal desease 7)Pregnant or nursing 8)Extensive leukopenia or extensive thrombocytopia 9)Use Sho-saiko-to 10)Other uncontrolled severe illness 11)Other inappropriate patient

Design outcomes

Primary

MeasureTime frame
Response rate

Secondary

MeasureTime frame
Safety profile

Countries

Japan

Contacts

Public ContactHiroki Ueda

Wakayama Medical University The third department of Internal Medicine

hu11@wakayama-med.ac.jp073-441-0619

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026