- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07614061
Safety and Efficacy of CD160-Enhanced Autologous Antigen-Specific T-Cells (BTC-Ag-T) in Advanced Biliary Tract Cancer
A Phase I, Open-label Study to Evaluate the Safety and Efficacy of CD160-enhanced Autologous BTC-Ag-T Cells in Advanced Biliary Tract Malignancies
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Guoming Shi, MD, PhD
- Numéro de téléphone: +86 021-64041990
- E-mail: shi.guoming@zs-hospital.sh.cn
Lieux d'étude
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Shanghai, Chine, 200032
- Recrutement
- Shanghai Zhongshan Hospital, Fudan University
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Contact:
- Guoming Shi, MD, PhD
- Numéro de téléphone: +86 021-64041990
- E-mail: shi.guoming@zs-hospital.sh.cn
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Chercheur principal:
- Jia Fan, MD, PhD
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Chercheur principal:
- Guoming Shi, MD, PhD
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Major Inclusion Criteria:
Subjects must meet all of the following criteria to be enrolled:
1. Age
- Age ≥ 18 years at the time of signing informed consent. 2. Diagnosis
Histologically or cytologically confirmed biliary tract malignancy (intrahepatic, perihilar, or distal extrahepatic cholangiocarcinoma, or gallbladder cancer).
3. Disease status
- Locally advanced unresectable or metastatic disease 4. Prior systemic therapy
Patients (including those with refractory BTC and those with postoperative recurrence) must have received prior gemcitabine-based chemotherapy in combination with a PD-1/PD-L1 inhibitor.
5. Measurable disease
- At least one measurable lesion per RECIST v1.1 at baseline imaging.
- Sufficient viable tumor tissue from biopsy for antigen-presenting tumor cell (APTC) manufacturing 6. Adequate venous access and overall condition to tolerate leukapheresis. 7. Washout and lymphocyte recovery before leukapheresis 8. ECOG performance status 0 or 1 9. Organ function
- Hematology (no growth-factor support or transfusion within 5 days of testing, unless otherwise stated): ANC ≥ 1.0 × 10⁹/L; platelets ≥ 75 × 10⁹/L; hemoglobin ≥ 8.0 g/dL (transfusion to reach this threshold is permitted).
- Hepatic: total bilirubin ≤ 2.0 × ULN (≤ 3.0 × ULN allowed for documented Gilbert syndrome); AST and ALT ≤ 5.0 × ULN.
- Renal: serum creatinine ≤ 1.5 × ULN, or estimated creatinine clearance (e.g., Cockcroft-Gault) ≥ 40 mL/min.
Adequate cardiopulmonary reserve to tolerate lymphodepleting conditioning and cell infusion in the investigator's judgment.
10. Viral serology
- No evidence of uncontrolled active viral infection.
- HIV-1/2 negative.
- Hepatitis B: HBV DNA is negative.
- Hepatitis C: HCV RNA is negative. 11. Contraception
Women of childbearing potential and men whose partners are of childbearing potential must agree to use highly effective contraception from the time of informed consent through at least 12 months after BTC-Ag-T infusion (or longer if required by local regulation).
12. Pregnancy status
Women of childbearing potential must have a negative serum or urine pregnancy test at screening.
13. Informed consent
- Able to understand and willing to sign a written informed consent document, and willing to comply with study procedures.
Exclusion Criteria:
Subjects who meet any of the following criteria will be excluded:
- Mixed/combined hepatocellular-cholangiocarcinoma, ampullary carcinoma, and other histologies not consistent with BTC
- Prior allogeneic transplant or recent gene-modified cell therapy
- Active CNS metastases
- Patients with uncontrolled or high-risk active infection are excluded, including hepatitis B virus (HBV), hepatitis C virus (HCV), Epstein-Barr virus (EBV), and active tuberculosis (TB).
- Active autoimmune disease requiring systemic immunosuppression
- Significant cardiovascular disease
- Significant pulmonary disease
- Severe hepatic decompensation
- Active variceal bleeding, or recent life-threatening portal-hypertension complications that cannot be stably controlled.
- Another primary malignancy within the past 3 years, except: tumors treated with curative intent and at low risk of recurrence (e.g., adequately treated basal- or squamous-cell skin cancer, in-situ cervical cancer, or low-Gleason localized prostate cancer, occult thyroid carcinoma).
- Severe hypersensitivity.
- Pregnant or lactating women
- Concurrent participation in another interventional study
- Any other condition that, in the investigator's judgment, renders the patient unsuitable for enrollment.
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 |
|---|---|
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Expérimental: CD160-Enhanced Autologous BTC-Ag-T
Autologous CD160-enhanced BTC-specific antigen-specific T cells (ACH-AgT001) administered IV after fludarabine/cyclophosphamide lymphodepletion.
Module A uses a 3+3 dose escalation.
Module B evaluates repeat lymphodepletion / re-induction at the selected dose.
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CD160-enhanced autologous antigen-specific T cells.
IV infusion.
Autres noms:
Combination of cyclophosphamide and Fludarabine as part of lymphodepletion
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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DLT incidence and MTD (Module A)
Délai: DLT window: Day 0 through Day 28
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Proportion of subjects with protocol-defined dose-limiting toxicities (Grade ≥3 cytokine release syndrome (CRS) or Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS), persistent Grade 4 cytopenia, or specified Grade ≥3 non-hematologic toxicity attributed to BTC-Ag-T); MTD identified per 3+3 rules.
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DLT window: Day 0 through Day 28
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Safety of repeat lympho-depletion(LD)/re-induction (Module B)
Délai: Through Day 150; long-term follow-up up to 15 years
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Incidence and severity of treatment-emergent adverse events graded per Common Terminology Criteria for Adverse Events (CTCAE) v6.0 and American Society for Transplantation and Cellular Therapy (ASTCT) criteria for CRS / ICANS, summarized by lymphodepletion cycle.
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Through Day 150; long-term follow-up up to 15 years
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Objective Response Rate (ORR)
Délai: 24 months
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The proportion of patients achieving Complete Response (CR) plus Partial Response (PR), as defined per RECIST v1.1 criteria.
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24 months
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Duration of Response (DoR)
Délai: 24 months
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Duration of response per RECIST v1.1 in responders.
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24 months
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Disease Control Rate (DCR)
Délai: 24 months
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Disease control rate (CR + PR + SD ≥ 12 weeks) per RECIST v1.1.
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24 months
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Progression-Free Survival (PFS)
Délai: 24 months
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Time from the date of Ag-T cell infusion to the first objective documentation of disease progression (per RECIST v1.1) or death due to any cause.
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24 months
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Overall Survival (OS)
Délai: 36 months
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Time from the date of Ag-T cell infusion to death from any cause.
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36 months
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Safety & Tolerability
Délai: Through 30 days post final infusion; long-term follow-up up to 15 years
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Adverse events graded per NCI-CTCAE v6.0; CRS / ICANS per ASTCT criteria; long-term gene-therapy follow-up per regulatory guidance.
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Through 30 days post final infusion; long-term follow-up up to 15 years
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Guoming Shi, MD, PhD, Department of Liver Surgery and Transplantation, Shanghai Zhongshan Hospital, Fudan University
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
Mots clés
Termes MeSH pertinents supplémentaires
- Tumeurs par site
- Tumeurs
- Tumeurs par type histologique
- Tumeurs du système digestif
- Maladies du système digestif
- Maladies des voies biliaires
- Tumeurs, glandulaires et épithéliales
- Adénocarcinome
- Carcinome
- Maladies de la vésicule biliaire
- Tumeurs des voies biliaires
- Cholangiocarcinome
- Tumeur de Klatskin
- Tumeurs de la vésicule biliaire
- Produits chimiques organiques
- Hydrocarbures
- Moutards phosphoramides
- Composés de moutarde d'azote
- Composés moutarde
- Hydrocarbures, halogénés
- Phosphoramides
- Composés organophosphores
- Cyclophosphamide
- fludarabine
Autres numéros d'identification d'étude
- ZSAB-AgT
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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