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Safety and Efficacy of CD160-Enhanced Autologous Antigen-Specific T-Cells (BTC-Ag-T) in Advanced Biliary Tract Cancer

28 de mayo de 2026 actualizado por: Jia Fan, Shanghai Zhongshan Hospital

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

BTC-Ag-T (ACH-AgT001) is an autologous experimental T-cell therapy designed for advanced biliary tract cancer. This is an open-label, single-arm Phase 1 study to evaluate the safety, tolerability, and preliminary efficacy of BTC-Ag-T in patients with advanced, unresectable, or metastatic biliary tract cancer who have failed standard-of-care therapy.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

18

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Shanghai, Porcelana, 200032
        • Reclutamiento
        • Shanghai Zhongshan Hospital, Fudan University
        • Contacto:
        • Investigador principal:
          • Jia Fan, MD, PhD
        • Investigador principal:
          • Guoming Shi, MD, PhD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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:

  1. Mixed/combined hepatocellular-cholangiocarcinoma, ampullary carcinoma, and other histologies not consistent with BTC
  2. Prior allogeneic transplant or recent gene-modified cell therapy
  3. Active CNS metastases
  4. 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).
  5. Active autoimmune disease requiring systemic immunosuppression
  6. Significant cardiovascular disease
  7. Significant pulmonary disease
  8. Severe hepatic decompensation
  9. Active variceal bleeding, or recent life-threatening portal-hypertension complications that cannot be stably controlled.
  10. 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).
  11. Severe hypersensitivity.
  12. Pregnant or lactating women
  13. Concurrent participation in another interventional study
  14. Any other condition that, in the investigator's judgment, renders the patient unsuitable for enrollment.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
CD160-enhanced autologous antigen-specific T cells. IV infusion.
Otros nombres:
  • CD160-Ag-T; ACH-AgT001
Combination of cyclophosphamide and Fludarabine as part of lymphodepletion

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
DLT incidence and MTD (Module A)
Periodo de tiempo: DLT window: Day 0 through Day 28
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.
DLT window: Day 0 through Day 28
Safety of repeat lympho-depletion(LD)/re-induction (Module B)
Periodo de tiempo: Through Day 150; long-term follow-up up to 15 years
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.
Through Day 150; long-term follow-up up to 15 years

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Objective Response Rate (ORR)
Periodo de tiempo: 24 months
The proportion of patients achieving Complete Response (CR) plus Partial Response (PR), as defined per RECIST v1.1 criteria.
24 months
Duration of Response (DoR)
Periodo de tiempo: 24 months
Duration of response per RECIST v1.1 in responders.
24 months
Disease Control Rate (DCR)
Periodo de tiempo: 24 months
Disease control rate (CR + PR + SD ≥ 12 weeks) per RECIST v1.1.
24 months
Progression-Free Survival (PFS)
Periodo de tiempo: 24 months
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.
24 months
Overall Survival (OS)
Periodo de tiempo: 36 months
Time from the date of Ag-T cell infusion to death from any cause.
36 months
Safety & Tolerability
Periodo de tiempo: Through 30 days post final infusion; long-term follow-up up to 15 years
Adverse events graded per NCI-CTCAE v6.0; CRS / ICANS per ASTCT criteria; long-term gene-therapy follow-up per regulatory guidance.
Through 30 days post final infusion; long-term follow-up up to 15 years

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Guoming Shi, MD, PhD, Department of Liver Surgery and Transplantation, Shanghai Zhongshan Hospital, Fudan University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de mayo de 2026

Finalización primaria (Estimado)

1 de diciembre de 2028

Finalización del estudio (Estimado)

1 de diciembre de 2029

Fechas de registro del estudio

Enviado por primera vez

22 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de mayo de 2026

Publicado por primera vez (Actual)

29 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

29 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

28 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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