Clinical trial · Interventional
CD276 CAR-T for Patients With Advanced CD276+ Solid Tumors
NCT04691713CI-TRIAL-00049219unknownN/AClinicalTrials.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)
This study is a clinical study of CD276 CAR-T in the treatment of patients with advanced solid tumors. The purpose is to evaluate the safety and effectiveness of targeting CD276 auto-chimeric antigen receptor T cells in the treatment of CD276-positive advanced solid tumors.
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 | — | UNRESOLVED | — |
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Targeting CD276 autologous chimeric antigen receptor T cells | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Targeting CD276 autologous chimeric antigen receptor T cells
- interventionNames
- Drug: Targeting CD276 autologous chimeric antigen receptor T cells
Primary outcomes (1)
- measure
- ORR 3
- timeFrame
- Three months after CAR T cell infusion
- description
- 3-month objective response rate
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 3 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * Age 3-70 * Expected survival time ≥ 12weeks * ECOG 0-2 * At least second-line or above chemotherapy failed * According to the evaluation criteria for the efficacy of solid tumors (RECIST 1.1), at least one measurable lesion (non-nodular lesion with longest diameter ≥10mm, or nodular lesion with short diameter ≥15mm) * Liver and kidney function, heart and lung function meet the following requirements: 1. Creatinine is within the normal range; 2. Left ventricular ejection fraction ≥ 45%; 3. Baseline blood oxygen saturation\>91%; 4. Total bilirubin≤1.5×ULN; ALT and AST≤2.5×ULN * Understand the trial and have signed the informed consent Exclusion Criteria: * Those who have graft-versus-host disease (GVHD) or need to use immunosuppressive agents * Hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) positive and peripheral blood HBV DNA titer test is not within the normal reference range; hepatitis C virus (HCV) antibody positive and peripheral blood HCV RNA positive; human immunodeficiency virus (HIV) Antibody positive; CMV DNA test positive; Syphilis test positive * Severe heart disease * Systemic diseases judged by the investigator to be unstable: including but not limited to severe liver, kidney or metabolic diseases that require medication * Within 7 days before screening, there are active infections or uncontrollable infections that require systemic treatment (except for mild urogenital infections and upper respiratory tract infections) * Women who are pregnant or breastfeeding, and female subjects who plan to become pregnant within 1 year after cell reinfusion, or male subjects whose partners plan to become pregnant within 1 year after cell reinfusion * Those who have received CAR-T therapy or other genetically modified cell therapy before screening * Subjects who are receiving systemic steroid therapy at the time of screening and the investigator determines that they need long-term systemic steroid therapy during the treatment period (except for inhaled or topical use) * Participated in other clinical studies within 3 months before screening * Central nervous system metastases are known to occur and for suspected central nervous system metastases, head MRI examination is required to rule out * Patients with partial or complete intestinal obstruction and complete biliary obstruction that cannot be relieved by active treatment * With more than a moderate amount of ascites, or after conservative medical treatment (such as diuresis, sodium restriction, excluding ascites drainage) for 2 weeks, the ascites still shows a progressive increase * According to the researcher's judgment, it does not meet the situation of cell preparation * Situations that other researchers think are not suitable for inclusion
References
Publications (0)
Data not yet available
No reference posted for this study.