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Clinical trial of hepatic arterial infusion chemotherapy with multidrug resistance-associated protein 3-derived peptide for hepatocellular carcinoma

Clinical trial of hepatic arterial infusion chemotherapy with multidrug resistance-associated protein 3-derived peptide for hepatocellular carcinoma - Hepatic arterial infusion chemotherapy with MRP3-derived peptide for hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005678
Enrollment
12
Registered
2011-06-01
Start date
2011-06-01
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

Hepatocellular carcinoma (HCC)

Interventions

Three times injection of MRP3-derived peptide during hepatic arterial infusion chemotherapy for HCC

Sponsors

Department of Gastroenterology, Kanazawa University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)HCC must be diagnosed and there is an indication of hepatic arterial infusion chemotherapy 2)Karnofsky Performance Status is equal to or more than 70% 3)Patients must be equal to or more than 20 years old and written informed consent must be obtained 4)WBC is equal to or more than 2,000/mm3 5)Platelet is equal to or more than 50,000/mm3 6)Hb is equal to or more than 8.5 g/dl 7)Level of liver damage must be A or B 8)Serum Cr is equal to or less than 1.5 mg/dl

Exclusion criteria

Exclusion criteria: 1)Severe complications associated with heart, kidney, lung, blood and coagulability 2)Infection of HIV 3)Past medical history of malignancy 4)Surgical treatment, chemotherapy and radiation therrapy within 4 weeks 5)Past medical history of Immunodeficiency, splenectomy and radiation of spleen 6)medical treatments with steroid 7)Patients who are during lactation 8)Patients who are during pregnancy and expected pregnancy 9)Past history of organ transplantation 10)Patients who are predicted a difficulty of following clinical course 11)Patients who are judged inappropriate for clinical trial

Design outcomes

Primary

MeasureTime frame
Evaluation of adverse events and immune responses

Countries

Japan

Contacts

Public ContactEishiro Mizukoshi

Kanazawa University Hospital Department of Gastroenterology

eishirom@m-kanazawa.jp076-265-2235

Outcome results

None listed

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