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CIB In Vivo CAR-T Lentiviral Injection in Patients With Advanced Malignant Tumors

A Phase 1, Open-Label, Single-Arm, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of CIB In Vivo CAR-T Lentiviral Injection in Patients With Advanced Malignant Tumors

This is an open-label, single-arm, phase 1 dose-escalation study to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of CIB in vivo CAR-T lentiviral injection in patients with advanced malignant tumors.

The study will enroll patients with histologically or cytologically confirmed advanced solid tumors that have progressed on or are intolerant to standard therapies. A "3+3" dose-escalation design will be used, with planned dose levels including 1×10⁵ TU/kg, 3×10⁵ TU/kg, 1×10⁶ TU/kg, 3×10⁶ TU/kg, 1×10⁷ TU/kg, and 3×10⁷ TU/kg. The primary objective is to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) based on dose-limiting toxicities (DLTs) observed within 28 days after administration. Secondary objectives include evaluating adverse events, objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and pharmacokinetic parameters of the study drug.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

This is a single-center, open-label, phase 1 dose-escalation study. Eligible patients will receive CIB in vivo CAR-T lentiviral injection at escalating dose levels. Safety assessments include adverse events, laboratory tests, vital signs, and physical examinations. Efficacy assessments include tumor response evaluation according to RECIST v1.1. Pharmacokinetic and immunogenicity assessments will also be performed.

Tipo de estudo

Intervencional

Inscrição (Estimado)

91

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100021
        • National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  1. Age ≥ 18 years and ≤ 75 years.
  2. At least one measurable target lesion according to RECIST version 1.1 at screening.
  3. Histologically or cytologically confirmed advanced or metastatic malignant tumor, with positive target expression confirmed by validated assay methods.
  4. Patients who have failed prior standard systemic therapy (including but not limited to VEGF-targeted tyrosine kinase inhibitors and/or immune checkpoint inhibitors), or are intolerant to standard therapy.
  5. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  6. Expected survival time ≥ 3 months as assessed by the investigator.
  7. Adequate organ function at baseline (no growth factor support or transfusion within 14 days prior to screening):

    a. Bone marrow function: i. Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L; ii. Hemoglobin (Hb) ≥ 90 g/L; iii. Platelet count (PLT) ≥ 75 × 10⁹/L. b. Liver function: Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × upper limit of normal (ULN); if liver metastases are present, ALT and AST ≤ 5 × ULN; total bilirubin (TBIL) ≤ 1.5 × ULN.

    c. Renal function: Serum creatinine ≤ ULN or creatinine clearance rate ≥ 80 mL/min.

  8. For female patients of childbearing potential, serum β-HCG test result must be negative within 7 days prior to enrollment.
  9. Patients must agree to use effective contraception from the signing of the informed consent form (ICF) until at least 90 days after the end of the study.
  10. Voluntarily sign the informed consent form (ICF) and be able to understand and comply with the requirements of the study protocol.

Exclusion Criteria:

  1. Asymptomatic untreated brain metastases; symptomatic central nervous system (CNS) metastases or carcinomatous meningitis; or other evidence of uncontrolled CNS/meningeal metastases that are considered unsuitable for enrollment by the investigator.
  2. Presence of clinically significant cardiovascular, pulmonary, neurological, or systemic disease at baseline that may increase study participation risk or interfere with safety assessments.
  3. Presence of severe chronic or active infection at baseline, including:

    1. Active hepatitis B (HBsAg positive with HBV DNA > ULN);
    2. Active hepatitis C (anti-HCV positive with detectable HCV RNA);
    3. Known history of or positive test for human immunodeficiency virus (HIV);
    4. Systemic anti-infective therapy required within 4 weeks prior to first administration, including hospitalization for infectious complications, bacteremia, severe pneumonia, or active tuberculosis.
  4. History of active autoimmune disease (e.g., systemic lupus erythematosus, rheumatoid arthritis, vasculitis) or receipt of long-term systemic corticosteroids (prednisone > 10 mg/day or equivalent) or other immunosuppressive agents within 4 weeks prior to first administration.
  5. Prior allogeneic tissue or solid organ transplantation.
  6. Evidence of severe immunodeficiency, such as primary immunodeficiency (e.g., severe combined immunodeficiency, SCID) or concurrent opportunistic infections.
  7. Prior gene therapy using lentiviral or retroviral vectors.
  8. Prior treatment with drugs targeting the same antigen.
  9. Requiring therapeutic anticoagulation that cannot be discontinued prior to administration.
  10. History of severe cardiovascular disease, including:

    1. NYHA class ≥ II congestive heart failure;
    2. Left ventricular ejection fraction (LVEF) < 50%;
    3. Corrected QT interval (QTcF) > 470 ms or long QT syndrome;
    4. Acute coronary syndrome, aortic dissection, severe arrhythmia, stroke, or other grade ≥ 3 cardiovascular events within 6 months prior to first administration;
    5. Uncontrolled hypertension.
  11. Prior anti-tumor therapy within 4 weeks or 5 half-lives (whichever is longer) prior to first administration, including chemotherapy, radiotherapy, biotherapy, endocrine therapy, immunotherapy; prior oral small-molecule targeted therapy within 2 weeks or 5 half-lives (whichever is longer); prior palliative radiotherapy within 14 days; prior participation in other anti-tumor clinical trials within 4 weeks; prior use of any anti-tumor traditional Chinese medicine within 2 weeks.
  12. Pregnant or breastfeeding women, or women of childbearing potential who refuse to use effective contraception during the study period.
  13. Any other disease or laboratory abnormality that, in the investigator's opinion, makes the patient unsuitable for participation in this study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Experimental: CIB in vivo CAR-T Lentiviral Injection
Intravenous administration of CIB in vivo CAR-T lentiviral injection as a single agent. Planned dose levels include 1×10⁵ TU/kg, 3×10⁵ TU/kg, 1×10⁶ TU/kg, 3×10⁶ TU/kg, 1×10⁷ TU/kg, and 3×10⁷ TU/kg.
CIB in vivo CAR-T lentiviral vector administered via intravenous infusion at escalating dose levels.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Incidence of Dose-Limiting Toxicities (DLTs) and Determination of Maximum Tolerated Dose (MTD)
Prazo: 28 days after administration
To evaluate the incidence of dose-limiting toxicities (DLTs) within 28 days after administration, and to determine the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D) of CIB in vivo CAR-T lentiviral injection.
28 days after administration

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Incidence and Frequency of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Prazo: From administration up to 24 months
To evaluate the incidence, frequency, and severity of all adverse events (AEs) and serious adverse events (SAEs) throughout the study period.
From administration up to 24 months
Objective Response Rate (ORR)
Prazo: Every 6 weeks after administration, up to 12 months
Percentage of patients with confirmed complete response (CR) or partial response (PR) according to RECIST v1.1.
Every 6 weeks after administration, up to 12 months
Disease Control Rate (DCR)
Prazo: Every 6 weeks after administration, up to 12 months
Description: Percentage of patients with confirmed CR, PR, or stable disease (SD) according to RECIST v1.1.
Every 6 weeks after administration, up to 12 months
Duration of Response (DoR)
Prazo: Up to 24 months after administration
Time from the first documented response (CR or PR) to disease progression or death.
Up to 24 months after administration
Progression-Free Survival (PFS)
Prazo: Up to 24 months after administration
Time from administration to the first documented disease progression or death due to any cause.
Up to 24 months after administration
Dynamic Changes in Peripheral Blood CAR-Positive T Cell Proportion
Prazo: Pre-dose, Days 7, 14, 28, 60, 90, and 180 after administration
Serial changes in the proportion of CAR-positive T cells in peripheral blood.
Pre-dose, Days 7, 14, 28, 60, 90, and 180 after administration
Dynamic Changes in Peripheral Blood Lentiviral Vector Copy Number
Prazo: Pre-dose, Days 7, 14, 28, 60, 90, and 180 after administration
Serial changes in the lentiviral vector copy number in peripheral blood.
Pre-dose, Days 7, 14, 28, 60, 90, and 180 after administration
Changes in Plasma Cytokine Levels
Prazo: Within 2 hours pre-dose, Days 2, 8, 14, and 28 after administration
Changes in plasma core cytokines including IFN-γ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, and TNF-α from baseline.
Within 2 hours pre-dose, Days 2, 8, 14, and 28 after administration

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Exploratory Pharmacodynamic Markers
Prazo: Pre-dose, Days 7, 14, 28, 60, and 90 after administration
Changes in peripheral blood T cell subsets (CD4+, CD8+, CD4/CD8 ratio), T cell functional status (4-1BB, PD1, TIGIT, CD62L, CD44), and immune cell activation markers (CD25+, HLA-DR+).
Pre-dose, Days 7, 14, 28, 60, and 90 after administration

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de julho de 2026

Conclusão Primária (Estimado)

30 de junho de 2027

Conclusão do estudo (Estimado)

31 de maio de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

14 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de junho de 2026

Primeira postagem (Real)

18 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

18 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

14 de junho de 2026

Última verificação

1 de abril de 2026

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • NCC6263

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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