Ireland
--:--IST
Active, not recruiting Phase 2

Dendritic Cell-immunotherapy for Advanced Hepatocellular Carcinoma

NCT07726329 · tracked via the Priya Life Science Taiwan tracker
Phase
Phase 2
Started
2019-07-01
Last updated
2026-07-24

Condition(s) studied

Liver Neoplasms

Investigational drug(s) / intervention(s)

dendritic cells

dendritic cells: autologous dendritic cell vaccination

Study summary

The prognosis of advanced hepatocellular carcinoma is poor. In this study, the eligible patients will be treated by tumor antigen-pulsed autologous dendritic cells and followed by TACE. The end points are to see tumor response and patient survival.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * advanced HCC patients, no response to standard treatment; WBC : 3000-12000/ul; platelet: \>80000/ul; anticipated survival \> 3 months, measurable tumors. Exclusion Criteria: * HIV; BCLC stage; acute infection; sepsis; other advanced malignancy; acute liver failure;

Primary outcome measure(s)

  • Incidence of Treatment-Related Adverse Events — up to 48 months.
    To evaluate the safety of the treatments by assessing the number of participants with treatment-related adverse events.
  • Objective Tumor Response — From date of first treatment until the date of first documented progression, assessed up to 48 months.
    To evaluate the tumor responses under the treatments as assessed by modified RECIST criteria.

Trial sites (1)

FacilityCityRegionStatus
Chang-Gung Memorial Hospital Taoyuan Taiwan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07726329 on ClinicalTrials.gov ↗ ← All trials in Taiwan