Clinical trial · Interventional
CAR-T Cell Immunotherapy for HCC Targeting GPC3
Chimeric Antigen Receptor-Modified T Cell (CAR-T) Immunotherapy for Hepatocellular Carcinoma (HCC) Targeting Glypican-3 (GPC3)
NCT02723942CI-TRIAL-00046003withdrawnPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Project terminated due to revision of local regulations
Summary
Brief summary (as posted)
The purpose of this study is to preliminarily evaluate the safety and efficacy of CAR-T cell immunotherapy for GPC3 positive hepatocellular carcinoma.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| CAR-T Cell Immunotherapy | — | UNRESOLVED | — |
| GPC3 Positive Hepatocellular Carcinoma | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CAR-T cell immunotherapy | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- CAR-T cell immunotherapy
- description
- Enrolled patients will receive CAR-T cell immunotherapy with a novel specific Chimeric antigen receptor aiming at GPC3 antigen by infusion.
- interventionNames
- Biological: CAR-T cell immunotherapy
- type
- NO_INTERVENTION
- label
- no intervention
- description
- no intervention
Primary outcomes (1)
- measure
- Radiological assessment
- timeFrame
- 3 months
- description
- Radiological assessment of the therapeutic effect by systemic or local computed Tomography(CT) or positron emission tomography scan.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria:
1. Age:18-70 years.
2. Gender:both.
3. GPC3 high expression hepatocellular carcinoma patients.
4. Non diffuse hepatocellular carcinoma,no extrahepatic metastasis or portal vein vascular invasion.
5. Degree of liver cirrhosis:class A or class B 7 according to Child-puge grading standard.
6. Routine blood test:white blood cell count(WBC)\>=3×10\^9/L, Lymphocyte percentage\>=15%, hemoglobinHbo(Hb)\>=90g/L, prothrombin time(PT) prolongation\<=50% normal value, Cluster of differentiation 3(CD3) positive T cell count\>=0.8×10\^9/L.
7. Liver and Pancreatic function:Alanine aminotransferase/Aspartate transaminase(ALT/AST)\<=5 times of the normal value, total bilirubin(TBiL)\<=3.0mg/dL, albumin(ALB)\>=35g/L, prothrombin time(PT):International Normalized Ratio(INR)\<=1.7 or prothrombin time(PT) prolongation\<=4s, Serum lipase\<=1.5 times of the normal value, Serum amylase\<=1.5 times of the normal value.
8. Renal function:Serum creatinine(SCr)\<=221μmol/L(2.5mg/L).
9. Karnofsky Performance Status(KPS)\>=60;Expected survival time\>=12 weeks.
10. Peripheral venous access ;no contraindication of lymphocyte separation.
11. No other serious complications.
12. Voluntarily signed informed consent.
Exclusion Criteria:
1. Pregnant and lactating women.
2. Lymphocyte separation or peripheral venous access cannot be performed in patients .
3. Patients in the active stage of infection or with coagulation disorders.
4. Patients with a previous history of hepatic coma.
5. Patients with severe gastrointestinal ulcers or gastrointestinal bleeding.
6. Patients with organ transplantation or waiting for organ transplantation.
7. Patients with anticoagulant therapy.
8. Patients with antiplatelet therapy.
9. Serum sodium(Na)\<125 mmol/L.
10. Serum potassium(K)\<3.5 mmol/L(except patients up to the standards after the use of supplements).
11. Patients with organ failure:
1. cardiac function:level three or above according to New York Heart Association (NYHA) criteria.
2. liver function:class C or above according to Child-puge grading standard.
3. renal function:Chronic kidney disease(CKD) phase 4 or more; renal insufficiency phase Ⅲ or more.
4. pulmonary function:severe respiratory failure symptoms, involving other organs.
5. Brain function:central nervous system abnormalities or disturbance of consciousness.
12. Patients with non controlled infectious diseases,for example,HIV positive, syphilis, hepatitis A, hepatitis B, hepatitis C, hepatitis E virus (HEV) positive etc.
13. Patients used corticosteroids or other immunosuppressive agents in the past 4 weeks.
14. Patients with autoimmune disease.
15. Patients with previous history of gene therapy.
16. The actual transfection rate of T cells was lower than 30% or the proliferation was less than 5 times after costimulation.
17. Patients participated in other drug trials in the past 4 weeks.
18. Patients received radiation treatment in the past 4 weeks.
19. Patients do not meet the criteria above.References
Publications (0)
Data not yet available
No reference posted for this study.