Clinical Trials in Taiwan / NCT07726329
Active, not recruiting
Phase 2
Dendritic Cell-immunotherapy for Advanced Hepatocellular Carcinoma
NCT07726329 · tracked via the Priya Life Science Taiwan tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Chang-Gung Memorial Hospital | Taoyuan | Taiwan |
More Chang Gung Memorial Hospital trials in Taiwan
Other trials for the same condition
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