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Clinical trial of a new treatment for the hepatocellular carcinoma patients with liver cirrhosis

Clinical trial of a new treatment for the hepatocellular carcinoma patients with liver cirrhosis - Clinical trial of a new treatment for the hepatocellular carcinoma patients with liver cirrhosis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024496
Enrollment
10
Registered
2016-11-01
Start date
2016-11-01
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

Interventions

Multiple administration of the optimal dosage

Sponsors

University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Between age of 20 to 75, who have agreement (2) Outpatients (3) Cirrhotic patients without uncontrollable ascites, who has no indication for resection, RFA, TACE or Sorafenib (4) Platelet counts less than 70,000/microL (5) Patient with the abnormal values in liver function tests (Alb, ALT, ChE, T-Bil, D-Bil) 6-month prior to registration (6) Less than four points of JIS score

Exclusion criteria

Exclusion criteria: (1) Acute hepatitis (2) Patients with HIV infection (3) Patients with a past history of cerebrovascular disease or cardiovascular disease (4) Bone marrow transplant recipients and immunosuppressed patients (5) Patient with plasma protein deficiency (eg. IgA deficiency) (6) Patients complicated with cerebrovascular disease, cardiovascular disease, pulmonary disease, renal disease, gastroenterological disease, hematological disease, and neurological or psychiatric disease (7) Patients with a cancer in other organs (8) Patients with HbA1c(NGSP) higher than 8.0 (9) Patients who is currently pregnant or consider pregnancy prior to the study (10) Patients who participated in another clinical trial within 6 months and received medications having pharmacologic effects on improving liver function or increasing platelet counts (11) Patients who have taken or who is currentry taking thrombopoietic agent (12) Patients with a past history of taking the Eltrombopag (13) Patients with allergic reaction to this medicine (14) Patients with allergic reaction to other medications (15) Patients with a past history of arterial or venous thromboembolism In addition, the patient who is judged to be inappropriate for this study

Design outcomes

Primary

MeasureTime frame
progression free survival

Countries

Japan

Contacts

Public ContactKurata Masanao

University of Tsukuba Department of Gastrointestinal and Hepato-Biliary-Pancreatic Surgery

mkurata@md.tsukuba.ac.jp029-853-3221

Outcome results

None listed

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