NCT04864054

GPC3-Targeted T-Cell Therapy (ECT204) in Adults With Advanced HCC

Recruiting
PHASE1Ages 18+InterventionalTreatment
Eureka Therapeutics Inc.
~60 participants
Updated 2026-06-09 on ClinicalTrials.gov
What's tested:ECT204 T cells

At a glance

Recruiting sites
6 of 8 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
To assess the safety and tolerability of ECT204.
Measured over Up to 2 years (active assessment period); additional long-term follow-up (LTFU) up to 15 years
Hepatocellular Carcinoma
Liver Cancer, Adult
Liver Neoplasm
Metastatic Liver Cancer
8 sites across 7 states
New York2
California1
Kansas1
Oregon1
Texas1
Washington1
Taiwan1
  • Pei Wang, PhD · STUDY_DIRECTOR · Eureka Therapeutics Inc.

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Histologically confirmed HCC, that is unresectable, recurrent, and/or metastatic.
GPC3-positive tumor expression confirmed by immunohistochemistry (IHC).
For the dose-escalation cohort: ≥10-20% tumor cells, ≥2+ IHC.
Beginning with the RP2D confirmatory cohort: ≥ 50% tumor cells, 2+/3+ IHC.
Must have received at least first-line systemic therapy for HCC and have experienced disease progression on, or intolerance to, that therapy.
Life expectancy of at least 4 months per the Investigator's opinion.
Eastern Cooperative Oncology Group (ECOG) performance status 0-1.
Measurable disease by RECIST v1.1.
Child-Pugh score of A6 or better.
Adequate organ function.

Exclusion

Pre-existing illness (e.g., symptomatic congestive heart failure) that would limit compliance with study requirements.
Active, uncontrolled systemic bacterial, fungal, or viral infection. Subjects with Human Immunodeficiency Virus (HIV), hepatitis B, or hepatitis C are eligible provided their infection is being treated and the viral load is controlled.
History of malignancy other than HCC within 5 years before screening, except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other malignancies with low risk of recurrence.
Known brain metastases or other active central nervous system (CNS) involvement, including leptomeningeal disease. Subjects with brain metastases that have been adequately treated (no evident neurological deficit and no steroid or anti-epileptic therapy for brain metastases) are eligible.
Pregnant or lactating women.
Currently receiving or ending (\< 14 days from date of consent) liver tumor-directed therapy (e.g., radiation, ablation, embolization), or hepatic surgery.
Concurrently receiving other investigational agents, biological, chemical, or radiation therapies, while participating in the study.
Active autoimmune disease requiring systemic immunosuppressive therapy.
Presence of portal vein tumor thrombus (PVTT) classified as grade Vp4, or any invasion into the inferior vena cava (IVC), except for subjects with IVC invasion who have been treated and radiographically stable for at least 6 months prior to screening.
Ascites requiring active treatment, such as a requirement for paracentesis or escalation of diuretic doses. Exception: Subjects maintained on a stable dose of diuretics with controlled, asymptomatic ascites are eligible.
Active gastrointestinal (GI) bleeding event ≥ Grade 3 per National Cancer Institute (NCI) Common Terminology for Adverse Events (CTCAE), version 5.0, within 6 months prior to screening.
Coagulation abnormality defined as international normalized ratio (INR) \> 1.7, unless the elevation is due to therapeutic anticoagulation that, in the Investigator's judgment, can be safely managed in the context of study procedures.
History of organ transplant.
HCC involving greater than 50% of the liver volume.
Experienced allergies to any component of the study drug (ECT204), mouse immunoglobulin, or iron-dextran, or have a history of severe hypersensitivity, including anaphylaxis.
Previously received other gene therapy (e.g., chimeric antigen receptor T-cell \[CAR-T\] therapy); exception: prior oncolytic virus therapy is permitted.).
Contraindication for undergoing leukapheresis procedure or receipt of conditioning agents
  • To assess the safety and tolerability of ECT204.Up to 2 years (active assessment period); additional long-term follow-up (LTFU) up to 15 years

    Type, frequency, and severity of adverse events (AEs), including treatment-emergent AEs (TEAEs), treatment-related AEs (TRAEs), serious adverse events (SAEs), adverse events of special interest (AESIs), clinically significant laboratory abnormalities recorded as AEs, and AEs leading to permanent discontinuation.