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Preclinical study on the treatment of neoantigen-reactive T cells for small cell lung carcinoma with novel IL-18 molecule

Preclinical study on the treatment of neoantigen-reactive T cells for small cell lung carcinoma with novel IL-18 molecule

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038618
Enrollment
Unknown
Registered
2020-09-26
Start date
2020-11-02
Completion date
Unknown
Last updated
2020-12-07

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

Conditions

small cell lung cancer

Interventions

Case series:modified neoantigen reactive T cells

Sponsors

The First Affiliated Hospital of The Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Histopathologically confirmed (included in the research center) as advanced small cell lung cancer, TNM stage as STAGE IIIb-IV; 2. Aged 18-75 years old; 3. Radiotherapy and chemotherapy were not effective, or chemotherapy was not suitable for or unwilling to radiotherapy, unwilling to other immunotherapy, at least one imaging measurable lesion.Expected survival >=3 months.Total bilirubin =50ml/min.

Exclusion criteria

Exclusion criteria: 1. Patients with HIV infection, hepatitis C virus (HCV) infection, uncontrolled coronary artery disease or asthma, uncontrollable cerebrovascular disease or other diseases that researchers consider not eligible for inclusion.Those with a history of bone marrow or organ transplantation; 2. People with coagulation disorders; 3. Subjects with immunodeficiency disease or autoimmune disease; 4. Patients who have had other immunotherapy within 1 month (such as immunocheckpoint inhibitor therapy, therapeutic antibody therapy, immunocell therapy and immunoregulator therapy); 5. May be allergic to immunotherapy; 6. Drug and alcohol abuse, clinical or psychological or social factors influence informed consent or research implementation; 7. Pregnant and lactating women; 8. Currently participating in or has participated in other clinical trials within a month; 9. Any uncertainties affecting patient safety or compliance; 10. Survivors of secondary brain metastases.

Design outcomes

Primary

MeasureTime frame
The incidence and severity of adverse events and specific laboratory abnormalities (CTCAE V4.03) in all treated subjects;

Countries

China

Contacts

Public ContactWei Zhang

The First Affiliated Hospital of The Second Military Medical University

zhangweismmu@126.com+86 13817804080

Outcome results

None listed

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