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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.

調査の概要

状態

まだ募集していません

詳細な説明

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.

研究の種類

介入

入学 (推定)

91

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100021
        • National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Incidence of Dose-Limiting Toxicities (DLTs) and Determination of Maximum Tolerated Dose (MTD)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Incidence and Frequency of Adverse Events (AEs) and Serious Adverse Events (SAEs)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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

その他の成果指標

結果測定
メジャーの説明
時間枠
Exploratory Pharmacodynamic Markers
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年7月1日

一次修了 (推定)

2027年6月30日

研究の完了 (推定)

2028年5月31日

試験登録日

最初に提出

2026年6月14日

QC基準を満たした最初の提出物

2026年6月14日

最初の投稿 (実際)

2026年6月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月18日

QC基準を満たした最後の更新が送信されました

2026年6月14日

最終確認日

2026年4月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • NCC6263

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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