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
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Ning Li
- Phone Number: +8601087788165
- Email: lining@cicams.ac.cn
Study Locations
-
-
Beijing Municipality
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Beijing, Beijing Municipality, China, 100021
- National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences
-
Contact:
- Ning Li
- Phone Number: +8601087788165
- Email: lining@cicams.ac.cn
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age ≥ 18 years and ≤ 75 years.
- At least one measurable target lesion according to RECIST version 1.1 at screening.
- Histologically or cytologically confirmed advanced or metastatic malignant tumor, with positive target expression confirmed by validated assay methods.
- 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.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Expected survival time ≥ 3 months as assessed by the investigator.
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.
- For female patients of childbearing potential, serum β-HCG test result must be negative within 7 days prior to enrollment.
- 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.
- Voluntarily sign the informed consent form (ICF) and be able to understand and comply with the requirements of the study protocol.
Exclusion Criteria:
- 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.
- Presence of clinically significant cardiovascular, pulmonary, neurological, or systemic disease at baseline that may increase study participation risk or interfere with safety assessments.
Presence of severe chronic or active infection at baseline, including:
- Active hepatitis B (HBsAg positive with HBV DNA > ULN);
- Active hepatitis C (anti-HCV positive with detectable HCV RNA);
- Known history of or positive test for human immunodeficiency virus (HIV);
- Systemic anti-infective therapy required within 4 weeks prior to first administration, including hospitalization for infectious complications, bacteremia, severe pneumonia, or active tuberculosis.
- 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.
- Prior allogeneic tissue or solid organ transplantation.
- Evidence of severe immunodeficiency, such as primary immunodeficiency (e.g., severe combined immunodeficiency, SCID) or concurrent opportunistic infections.
- Prior gene therapy using lentiviral or retroviral vectors.
- Prior treatment with drugs targeting the same antigen.
- Requiring therapeutic anticoagulation that cannot be discontinued prior to administration.
History of severe cardiovascular disease, including:
- NYHA class ≥ II congestive heart failure;
- Left ventricular ejection fraction (LVEF) < 50%;
- Corrected QT interval (QTcF) > 470 ms or long QT syndrome;
- Acute coronary syndrome, aortic dissection, severe arrhythmia, stroke, or other grade ≥ 3 cardiovascular events within 6 months prior to first administration;
- Uncontrolled hypertension.
- 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.
- Pregnant or breastfeeding women, or women of childbearing potential who refuse to use effective contraception during the study period.
- Any other disease or laboratory abnormality that, in the investigator's opinion, makes the patient unsuitable for participation in this study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / 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
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
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
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
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- NCC6263
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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