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A Phase II Study of Ivonescimab in Combination With GEMOX as Neoadjuvant and Conversion Therapy for Biliary Tract Cancer

30 de septiembre de 2026 actualizado por: Haitao Zhao, MD

A Single-Arm, Multi-Cohort, Phase II Study of Ivonescimab in Combination With GEMOX Chemotherapy as Neoadjuvant and Conversion Therapy for Biliary Tract Cancer

The purpose of this study is to explore the efficacy and safety of Ivonescimab in combination with GEMOX chemotherapy as neoadjuvant and conversion therapy for patients with biliary tract cancer. It aims to evaluate the impact of this combination regimen on postoperative recurrence, patient survival, and medication safety.

This is a single-center, phase II, interventional, single-arm, multi-cohort clinical study. A total of 87 eligible participants will be enrolled and assigned to either the neoadjuvant therapy cohort (45 participants) or the conversion therapy cohort (42 participants).

Descripción general del estudio

Estado

Reclutamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

87

Fase

  • Fase 2

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

  • Nombre: Haitao Zhao, DR
  • Número de teléfono: +86-10-69156042
  • Correo electrónico: zhaoht@pumch.cn

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100730
        • Reclutamiento
        • Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
        • Contacto:
          • Haitao Zhao, DR
          • Número de teléfono: +86-10-69156042
          • Correo electrónico: zhaoht@pumch.cn

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

18 años a 80 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • 1. Subjects voluntarily participate in the study, agree to sign a written informed consent form, demonstrate good compliance, and are willing to cooperate with follow-up.

  • 2. Male or female aged >= 18 and <= 80 years at the time of signing the ICF.

  • 3. Histologically or cytologically confirmed biliary tract cancer (BTC, including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder cancer), and radiologically assessed as locally advanced or with oligometastases (defined as Stage IIIA or higher lesions according to the 8th edition of the AJCC staging system). Subjects must agree to provide archived or fresh tumor biopsy specimens and peripheral blood samples for biomarker testing.

  • 4. Lesion assessment meets one of the following conditions:

  • Neoadjuvant Therapy Cohort: The tumor is graded as locally advanced with no distant metastasis, and theoretically can achieve radical resection through complex resection combined with vascular reconstruction, but both the surgical risk and postoperative recurrence risk are high (single tumor diameter > 5 cm; imaging suggests vascular invasion or hilar lymph node metastasis; tumor number > 3 or any single tumor > 3 cm; preoperative CA19-9 > 37 U/mL or exceeding the upper limit of normal [applicable to centers where the normal range is not < 37 U/mL]).

  • Conversion Therapy Cohort: The tumor is graded as locally advanced, unresectable, or combined with oligometastatic status (oligometastasis is defined as: metastatic lesions confined to a single organ or specific regional lymph nodes, and the number of metastatic lesions is <= 5), with the possibility of achieving radical resection of the primary lesion and no evidence of disease (NED) status for metastatic lesions after comprehensive treatment.

  • 5. At least one measurable lesion (according to RECIST v1.1 criteria, the longest diameter of the measurable lesion on spiral CT scan >= 10 mm or the shortest diameter of enlarged lymph nodes >= 15 mm).

  • 6. No prior systemic therapy for biliary tract cancer.

  • 7. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 1.

  • 8. Child-Pugh class A liver function.

  • 9. Normal bone marrow, liver, and kidney function, meeting the following clinical laboratory evaluation criteria within 7 days prior to treatment (the conditions cannot be met by administering any blood components, cell growth factors, albumin, or other corrective medications within 14 days prior to obtaining the laboratory tests; patients developing obstructive jaundice after percutaneous transhepatic cholangial drainage [PTCD] or endoscopic retrograde cholangiopancreatography [ERCP] treatment may be considered for enrollment if liver function indicators meet the inclusion criteria):

    1. Absolute neutrophil count (ANC) >= 1.5 x 10^9/L, platelet count >= 90 x 10^9/L, hemoglobin >= 90 g/L; AST and ALT <= 3 x ULN (upper limit of normal); TBil <= 1.5 x ULN;
    2. Hemoglobin > 9 g/dL without blood transfusion or use of erythropoietin within the past 14 days;
    3. Serum creatinine <= 1.5 x ULN and creatinine clearance rate (calculated using Cockcroft-Gault formula) >= 60 ml/min;
    4. Good coagulation function, International Normalized Ratio (INR) <= 1.2 or Prothrombin Time (PT) <= 1.2 x ULN;
    5. Normal thyroid function, defined as Thyroid Stimulating Hormone (TSH) within the normal range. If baseline TSH is outside the normal range, subjects with total T3 (or FT3) and FT4 within the normal range are also eligible;
    6. Myocardial enzyme spectrum within the normal range (isolated laboratory abnormalities judged by the investigator to have no clinical significance are also permitted).
  • 10. Subjects with previous or current Hepatitis B Virus (HBV) or Hepatitis C Virus (HCV) infection must have received standard antiviral therapy, and the investigator must confirm that the current liver disease status is stable and suitable for receiving the study treatment.

  • 11. Women of childbearing potential: agree to use effective contraceptive methods during the study period and for 120 days after the last dose, and have a negative urine or serum pregnancy test within 7 days prior to the first dose.

  • 12. Men: agree to use effective contraceptive methods during the study period and for 120 days after the last dose.

Exclusion Criteria:

  • 1. Diagnosed with mixed periampullary cancer, or mixed hepatocellular-cholangiocarcinoma.
  • 2. Prior systemic anti-tumor therapy for BTC.
  • 3. Prior treatment with gemcitabine-based chemotherapy, platinum-based chemotherapy, or any tumor immunotherapy/targeted therapy (e.g., PD-1/PD-L1 inhibitors, VEGF inhibitors, etc.).
  • 4. History of severe allergy to other monoclonal antibodies. Known severe allergy or intolerance to gemcitabine, platinum drugs, or any of their components/excipients.
  • 5. Known allergy or intolerance to recombinant humanized PD-1 monoclonal antibody drugs, VEGF monoclonal antibody drugs, and their components (or any excipients), or a history of severe allergy to other monoclonal antibodies.
  • 6. Pericardial effusion, uncontrollable pleural effusion, or clinically significant ascites within 7 days prior to treatment, defined as meeting the following criteria: (a) ascites detectable by physical examination during the screening period, or (b) ascites requiring therapeutic paracentesis during the screening period.
  • 7. Clinical evidence of portal hypertension with esophageal or gastric varices within 6 months prior to the start of treatment.
  • 8. Any bleeding or thrombotic disorders within 6 months prior to the start of treatment, or currently taking any anticoagulants (e.g., warfarin or similar drugs) requiring monitoring of the International Normalized Ratio (INR) during treatment.
  • 9. History of any malignant tumor, except for the BTC studied in this clinical trial and cured locally recurrent cancers (e.g., resected basal cell or squamous cell skin cancer, superficial bladder cancer, cervical cancer or breast cancer in situ, occult thyroid cancer).
  • 10. Known central nervous system metastasis and/or leptomeningeal disease prior to treatment.
  • 11. History of any active immunodeficiency or autoimmune disease, and/or any immunodeficiency or autoimmune disease that may relapse at the time of screening.
  • 12. Any severe chronic or active infection (except viral hepatitis) requiring systemic antibacterial, antifungal, or antiviral therapy (e.g., tuberculosis) prior to the start of treatment.
  • 13. Electrocardiogram (ECG) during screening shows a heart rate-corrected QT interval (QTc) (corrected using Fridericia's formula) exceeding 450 milliseconds. Note: If the QTc interval exceeds 450 milliseconds on the first ECG, a repeat ECG will be performed to confirm the result.
  • 14. Presence of any of the following cardiovascular risk factors: cardiogenic chest pain within 28 days prior to treatment, defined as moderate pain limiting activities of daily living (ADL); symptomatic pulmonary embolism within 28 days prior to treatment; acute myocardial infarction within 6 months prior to treatment; history of New York Heart Association (NYHA) Class III or IV heart failure within 6 months prior to treatment; Grade >= 2 ventricular arrhythmia within 6 months prior to treatment; cerebrovascular accident (CVA) or transient ischemic attack (TIA) within 6 months prior to treatment.
  • 15. Organ transplantation or hematopoietic stem cell transplantation (HSCT) or any major surgery within 28 days prior to treatment.
  • 16. Known psychiatric or substance abuse disorders that may interfere with cooperation in the trial.
  • 17. Receipt of live vaccine within 28 days prior to treatment. Note: Seasonal influenza vaccines are generally inactivated influenza vaccines and are permitted.
  • 18. Known history of Human Immunodeficiency Virus (HIV) infection or syphilis infection.
  • 19. Any history of disease, treatment, or laboratory abnormalities that, in the opinion of the principal investigator, may confound the test results, interfere with the subject's participation throughout the trial, or are not in the best interest of the subject.
  • 20. Currently participating in and receiving treatment in another drug or device study, or having participated in such studies within 4 weeks prior to the first dose of the study drug.
  • 21. Pregnant or breastfeeding from the screening visit to 120 days after the last dose, or expecting to conceive or give birth within the planned duration of the trial.
  • 22. Poor compliance as judged by the investigator, or presence of other conditions making the patient unsuitable to participate in this trial.
  • 23. Presence of multiple medical contraindications making it unsuitable to undergo contrast-enhanced imaging (CT or MRI) examinations.
  • 24. Presence of surgical contraindications; patients deemed unsuitable for surgery by the investigators.

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: Ivonescimab + GEMOX

Participants in both the neoadjuvant therapy cohort and the conversion therapy cohort belong to this single experimental arm. All participants will receive 3 to 6 cycles of Ivonescimab in combination with GEMOX chemotherapy prior to surgical evaluation.

Administered at a dose of 20 mg/kg via intravenous (IV) infusion on Day 1 of each 21-day cycle (Q3W) in combination with GEMOX chemotherapy for 3 to 6 cycles. For eligible patients in the conversion therapy cohort who do not undergo surgery after evaluation, Ivonescimab is continued as maintenance monotherapy (20 mg/kg, IV, Q3W, Day 1) until disease progression, unacceptable toxicity, death, withdrawal of consent, or investigator decision.

Otros nombres:
  • AK112

The GEMOX regimen consists of Gemcitabine (1000 mg/m²) and Oxaliplatin (100 mg/m²). Both drugs are administered via intravenous (IV) infusion on Day 1 of each 21-day cycle (Q3W). This chemotherapy regimen is administered in combination with Ivonescimab for 3 to 6 cycles prior to surgical evaluation.

Otros nombres:
  • Gemcitabine and Oxaliplatin

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
R0 Resection Rate
Periodo de tiempo: Up to 6 weeks post-surgery

The proportion of participants in the neoadjuvant therapy cohort who undergo surgical resection and achieve microscopically margin-negative (R0) resection.

Up to 6 weeks post-surgery
Objective Response Rate
Periodo de tiempo: Up to 24 weeks (assessed after 3-6 cycles of treatment)

The proportion of participants in the conversion therapy cohort achieving a Complete Response (CR) or Partial Response (PR) based on RECIST v1.1 criteria as assessed by investigators.

Up to 24 weeks (assessed after 3-6 cycles of treatment)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Objective Response Rate
Periodo de tiempo: Up to 10 weeks from baseline (assessed pre-operatively)

The proportion of participants in the neoadjuvant cohort achieving CR or PR based on RECIST v1.1.

Up to 10 weeks from baseline (assessed pre-operatively)
R0 Resection Rate
Periodo de tiempo: Up to 4 weeks post-surgery (assessed upon availability of postoperative pathology report)

The proportion of participants in the conversion cohort who achieve resectability and obtain an R0 resection post-surgery.

Up to 4 weeks post-surgery (assessed upon availability of postoperative pathology report)
Pathological Response Rate
Periodo de tiempo: Up to 4 weeks post-surgery

The proportion of participants who achieve Major Pathological Response (MPR) or Pathological Complete Response (pCR) confirmed by postoperative pathology.

Up to 4 weeks post-surgery
Disease Control Rate
Periodo de tiempo: Up to 19 weeks from baseline (assessed pre-operatively)

The proportion of participants achieving CR, PR, or Stable Disease (SD) based on RECIST v1.1.

Up to 19 weeks from baseline (assessed pre-operatively)
Incidence and Severity of Adverse Events
Periodo de tiempo: Up to 28 days after the last dose of study treatment

Incidence of AEs, Serious Adverse Events (SAEs), drug-related AEs, and specific AEs assessed per NCI CTCAE v5.0. This includes continuous monitoring of vital signs and laboratory parameters.

Up to 28 days after the last dose of study treatment
Event-Free Survival
Periodo de tiempo: Up to 24 months

The time from study enrollment to the first occurrence of disease progression precluding surgery, local/regional recurrence after surgery, distant metastasis, or death from any cause.

Up to 24 months
Progression-Free Survival
Periodo de tiempo: Up to 24 months

The time from study enrollment of the conversion therapy cohort to the first documented objective tumor progression per RECIST v1.1 or death from any cause.

Up to 24 months
Relapse-Free Survival
Periodo de tiempo: Up to 24 months

The time from surgical resection to the first occurrence of disease recurrence (local, regional, or distant) or death from any cause among patients who underwent surgery.

Up to 24 months
Overall Survival
Periodo de tiempo: Up to 24 months

The time from study enrollment to death from any cause.

Up to 24 months

Colaboradores e Investigadores

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

Patrocinador

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 octubre de 2026

Finalización primaria (Estimado)

1 de octubre de 2028

Finalización del estudio (Estimado)

1 de diciembre de 2029

Fechas de registro del estudio

Enviado por primera vez

24 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de septiembre de 2026

Publicado por primera vez (Actual)

2 de octubre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de octubre de 2026

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

30 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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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