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Clinical study for autologous RCAT cells plus PD-1 antibody in patients with advanced renal cell carcinoma following failure of targeted therapy

Clinical study for combined immunotherapy in advanced renal cell carcinoma after failure of targeted therapy

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024385
Enrollment
Unknown
Registered
2019-07-08
Start date
2015-07-01
Completion date
Unknown
Last updated
2019-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

renal carcinoma

Interventions

Case series:combined immunotherapy by RCAR plus PD-1 antibody

Sponsors

He'nan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. signing the informed consent voluntarily; 2. aged 18 to 80 years old; 3. diagnosed with renal cell carcinoma by pathology, progressing or intolerant to previously targeted therapy; 4. at one measurable lesion by RECIST 1.1 version; 5. ECOG=12 weeks; 7. sufficient organ function.

Exclusion criteria

Exclusion criteria: 1. receiving immunosuppressive or glucocorticoid therapy; 2. wounds caused by severe infections difficult to heal and suppurative inflammation difficult to control 3. Organic heart disease, cardiac insufficiency, cardiac conduction block above II, myocardial infarction occurred within 3 months; 4. Lung dysfunction caused by interstitial lung disease, lung ventilation reserve is lower than 80% of the expected value; 5. Participated in other clinical studies in the past month; 6. Severe hypersensitivity reactions have occurred after the application of other monoclonal antibody drugs; 7. previously received PD-1 or PD-L1 antibody treatment; 8. Active brain metastasis; 9. Uncontrolled chest, peritoneal effusion, pericardial effusion requiring repeated drainage; 10. Have received live vaccine or attenuated vaccination within 28 days before enrollment; 11. Major surgery was performed within 28 days prior to enrollment; 12. Conducted a solid organ transplant; 13. Pregnant lactating women; 14. With previous mental illness; 15. With history of other malignancy; 16. Other investigators believe that it is not appropriate to participate in the study (HIV infection, intravenous drug addicts, etc.), or other conditions that affect the analysis of the results of this clinical study.

Design outcomes

Primary

MeasureTime frame
response rate;progression-free survival;

Secondary

MeasureTime frame
survival time;

Countries

China

Contacts

Public ContactZhao Lingdi

He'nan Cancer Hospital

lingdizhao@126.com+86 13323847809

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026