Clinical trial · Interventional
ET 140202 -T Cell Combined With TAE or Sorafenib in the Treatment of Liver Cancer
Clinical Study of ET 140202 -T Cell Combined With TAE or Sorafenib in the Treatment of Advanced Liver Cancer
NCT03965546CI-TRIAL-00039974unknownEarly Phase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the efficacy and safety of ET 140202 -T cell combined With TAE or Sorafenib in the treatment of liver cancer
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Liver Cancer | Malignant Liver Neoplasm | CURATED_EXACT | 0.92 |
| Liver Neoplasms | Liver Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Metastatic Liver Cancer | Malignant Liver Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ET140202-T cell | Biological | — | UNRESOLVED |
| Sorafenib combined with ET140202-T cell | Combination Product | — | UNRESOLVED |
| TAE combined with ET140202-T cell | Combination Product | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- ET140202-T cell combine with Sorafenib
- description
- Sorafenib treatment everyday and autologous ET140202-T cell administered by intravenous (IV) infusion
- interventionNames
- Combination Product: Sorafenib combined with ET140202-T cell
- type
- EXPERIMENTAL
- label
- ET140202-T cell combine with TAE
- description
- TAE treatment ahead every two times of autologous ET140202-T cell administered by intravenous (IV) infusion
- interventionNames
- Combination Product: TAE combined with ET140202-T cell
- type
- EXPERIMENTAL
- label
- solo ET140202-T cell
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * AFP-expressing HCC and serum AFP \>10 x ULN * Abandon or failure in first or second line treatment * Molecular HLA class I typing confirms participant carries at least one HLA-A02 allele * Child-Pugh score of A or B, ECOG 0-2, Life expectancy \> 6 months * Measurable disease as defined by: at least 1 liver lesion that can be accurately and serially measured. * Negative serum pregnancy test for women with childbearing potential * Adequate organ function as defined below: 1. A pretreatment measured creatinine clearance (absolute value) of ≥50 ml/minute. 2. Patients must have a serum direct bilirubin ≤3 x ULN, ALT and AST ≤5 x ULN. 3. Ejection Fraction measured by echocardiogram or MUGA \>50% (evaluation done within 6 weeks of screening does not need to be repeated) 4. DLCO or FEV1 \>45% predicted 5. Absolute neutrophil count (ANC) ≥ 1500/mm3 (10\^9/L), Platelet count ≥ 50,000/mm3 (10\^9/L) 6. INR ≤1.5 x ULN 7. Informed Consent/Assent: All subjects must have the ability to understand and the willingness to sign a written informed consent. Exclusion Criteria: * Patients with decompensated cirrhosis: Child-Pugh Score C * Patients with tumor infiltration in the portal vein, hepatic veins or inferior vena cava that completely blocks circulation in liver. * Patients with an organ transplantation history * Patients with dependence on corticosteroids * Patients with active autoimmune diseases requiring systemic immunosuppressive therapy * Patients who are currently receiving or received within past 30 days anti-cancer therapy, local treatments for liver tumors (radiotherapy, embolism, ablation) or liver surgery * Patients currently receiving other investigational treatments (biotherapy, chemotherapy, or radiotherapy) * Participants with other active malignancies (except non-melanoma skin cancer and cervical cancer) within two years. Patients with a history of successfully-treated tumors with no sign of recurrence in the last two years may be enrolled. * Patients with other uncontrolled diseases, such as active infections Acute or chronic active hepatitis B or hepatitis C. * Women who are pregnant or breast-feed * HIV-infection
References
Publications (0)
Data not yet available
No reference posted for this study.