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.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

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.

Study Type

Interventional

Enrollment (Estimated)

91

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

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

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of Dose-Limiting Toxicities (DLTs) and Determination of Maximum Tolerated Dose (MTD)
Time Frame: 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

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence and Frequency of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: 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

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Exploratory Pharmacodynamic Markers
Time Frame: 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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

July 1, 2026

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

May 31, 2028

Study Registration Dates

First Submitted

June 14, 2026

First Submitted That Met QC Criteria

June 14, 2026

First Posted (Actual)

June 18, 2026

Study Record Updates

Last Update Posted (Actual)

June 18, 2026

Last Update Submitted That Met QC Criteria

June 14, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NCC6263

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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