Can a cancer vaccine prime the body to better fight liver tumors?
NCT ID NCT07726329
First seen Jul 24, 2026 ยท Last updated Jul 24, 2026
Summary
This trial tests whether giving a personalized dendritic cell vaccine before a standard liver-directed therapy (TACE) can improve outcomes for people with advanced liver cancer that has not responded to other treatments. The vaccine is made from the patient's own immune cells and trained to recognize their tumor. The study will measure safety, tumor shrinkage, and overall survival.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a dendritic cell vaccine followed by transcatheter arterial chemoembolization (TACE)
- What this could lead to
- If it works, this combination approach could offer a new treatment option for people with advanced liver cancer who have run out of standard options.
- What could go wrong
- This is a mid-stage trial with 100 participants, so results are not yet proven. The treatment involves two complex procedures and may cause side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2019
- Expected to finish
-
Feb 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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;
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Chang-Gung Memorial Hospital
Taoyuan, 33357, Taiwan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Patient's own immune cells keep liver cancer at bay?
- Can a new drug boost the power of existing liver cancer therapy?
- Could a daily mineral make liver cancer therapy work better?
- Can a triple drug attack stop liver cancer from coming back?
- Can a custom vaccine train the body to fight liver cancer?
- Personalized liver cancer treatment: a quest for predictive biomarkers