- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07657585
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.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Ning Li
- Numéro de téléphone: +8601087788165
- E-mail: lining@cicams.ac.cn
Lieux d'étude
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Beijing Municipality
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Beijing, Beijing Municipality, Chine, 100021
- National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences
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Contact:
- Ning Li
- Numéro de téléphone: +8601087788165
- E-mail: lining@cicams.ac.cn
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La 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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
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CIB in vivo CAR-T lentiviral vector administered via intravenous infusion at escalating dose levels.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Incidence of Dose-Limiting Toxicities (DLTs) and Determination of Maximum Tolerated Dose (MTD)
Délai: 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.
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28 days after administration
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Incidence and Frequency of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Délai: From administration up to 24 months
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To evaluate the incidence, frequency, and severity of all adverse events (AEs) and serious adverse events (SAEs) throughout the study period.
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From administration up to 24 months
|
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Objective Response Rate (ORR)
Délai: Every 6 weeks after administration, up to 12 months
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Percentage of patients with confirmed complete response (CR) or partial response (PR) according to RECIST v1.1.
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Every 6 weeks after administration, up to 12 months
|
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Disease Control Rate (DCR)
Délai: Every 6 weeks after administration, up to 12 months
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Description: Percentage of patients with confirmed CR, PR, or stable disease (SD) according to RECIST v1.1.
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Every 6 weeks after administration, up to 12 months
|
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Duration of Response (DoR)
Délai: Up to 24 months after administration
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Time from the first documented response (CR or PR) to disease progression or death.
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Up to 24 months after administration
|
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Progression-Free Survival (PFS)
Délai: Up to 24 months after administration
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Time from administration to the first documented disease progression or death due to any cause.
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Up to 24 months after administration
|
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Dynamic Changes in Peripheral Blood CAR-Positive T Cell Proportion
Délai: Pre-dose, Days 7, 14, 28, 60, 90, and 180 after administration
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Serial changes in the proportion of CAR-positive T cells in peripheral blood.
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Pre-dose, Days 7, 14, 28, 60, 90, and 180 after administration
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Dynamic Changes in Peripheral Blood Lentiviral Vector Copy Number
Délai: 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
|
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Changes in Plasma Cytokine Levels
Délai: Within 2 hours pre-dose, Days 2, 8, 14, and 28 after administration
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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.
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Within 2 hours pre-dose, Days 2, 8, 14, and 28 after administration
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Exploratory Pharmacodynamic Markers
Délai: Pre-dose, Days 7, 14, 28, 60, and 90 after administration
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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
|
Collaborateurs et enquêteurs
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- NCC6263
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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