NCT07113977Not yet recruitingEarly phase 1
Clinical Study of a Novel Humanized CD70-Targeted CAR-T Cell Incorporating TLR2 for Advanced Renal Cell Carcinoma Therapy
Source: ClinicalTrials.gov · Last updated 11 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
In this clinical study, participants with advanced renal cell carcinoma will receive a novel humanized CD70-targeted CAR-T-cell product that incorporates the TLR2 co-stimulatory domain. Peripheral blood mononuclear cells will be collected from each subject, genetically modified to express the CAR construct, and expanded ex vivo; after passing multiple quality-control assays, the CAR-T cells will be infused at the pre-specified dose. Post-infusion, the efficacy and safety of CD70-directed CAR-T-cell therapy will be systematically evaluated using clinical symptom assessments, quality-of-life questionnaires, biomarker analyses, laboratory tests, imaging studies, adverse-event monitoring, and long-term follow-up.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Early phase 1
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 24 Jul 2025
- Start date
- 15 Aug 2025
- Primary completion date
- 31 Aug 2028
- Lead sponsor
- Wei Guan
- Diseases
- Kidney cancer
- NCT number
- NCT07113977
What you commit to
- Study type: Interventional · Early phase 1
- Planned participants: 30
- From 15 Aug 2025 to the primary completion date, 31 Aug 2028
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- 5.Prior gene therapy of any form;
- 10.Prohibited medications/treatments: Corticosteroids: ≥2 mg/kg prednisone (or equivalent \>20 mg/day) within 2 weeks before leukapheresis.
- Chemo/radiotherapy: Anti-tumor radiotherapy or salvage chemotherapy within 3 weeks before leukapheresis.
- Immunosuppressants: Use within 4 weeks before leukapheresis. Other trials/major surgery: Participation in another clinical trial or major non-diagnostic surgery within 4 weeks before leukapheresis.
- Specific agents: Alemtuzumab within 6 months, or clofarabine/cladribine within 3 months before leukapheresis.
Other illness
- 2.Uncontrolled fungal, bacterial, Treponema pallidum, viral, or other infections;
- 3.Active hepatitis: HBV DNA \>500 IU/mL. Positive HCV RNA (confirmed by repeat testing);
- 4.HIV infection, known acquired immunodeficiency syndrome (AIDS), or syphilis infection;
- 6.History of severe allergic reactions to biologics (including antibiotics), antibodies, cytokines, or other macromolecular agents;
- 7.Clinically significant CNS disorders: epilepsy, paresis, aphasia, stroke, severe traumatic brain injury, dementia, Parkinson's disease, cerebellar disorders, organic brain syndrome;
- 8.Uncontrolled psychiatric illness;
Other
- 1.Pregnant or lactating women;
- 9.Substance abuse/addiction;
Who the study is looking for
- 1\. Voluntary participation with written informed consent provided by the patient or legally authorized representative;
- 2.Age 18-75 years (inclusive) at the time of consent, regardless of sex;
- 3.Advanced-stage renal cell carcinoma (RCC) with no curative treatment options, who have received ≥1 prior line of therapy and meet one or more of the following:
- Recurrence after first-line or later-line treatment(s).
- Progression or persistent progression following prior therapy;
- 4.Histopathologically confirmed advanced RCC per WHO 2016 classification, with at least one measurable lesion evaluable by CT or MRI;
- 5.CD70 positivity in tumor tissue confirmed by immunohistochemistry (IHC);
- 6.Adequate organ function: Hepatic: ALT/AST \<3× ULN and total bilirubin ≤34.2 μmol/L. Renal: Creatinine clearance (Cockcroft-Gault) ≥60 mL/min. Pulmonary: Oxygen saturation ≥95% with no active pulmonary infection. Cardiac: LVEF ≥50%, no significant pericardial effusion, and no clinically relevant ECG abnormalities;
- 7.Contraception: Women of childbearing potential must have a negative pregnancy test (urine/serum) at screening and agree to use effective contraception for ≥1 year post-infusion.
- Men with partners of childbearing potential must use barrier contraception for ≥1 year post-infusion;
- 8.Performance status: ECOG score 0-3;
- 9.Life expectancy \>3 months;
- 10.Willingness to comply with leukapheresis, medical assessments, and follow-up visits.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.