Ori-C101Chimeric Antigen Receptor (CAR) Modified T Cells for the Treatment of HCC

Официальное название

A Phase Ib/II, Open-Label, Multi-Center Study to Investigate the Safety, PK, and Efficacy of Ori-C101 in Advanced Hepatocellular Carcinoma (HCC) Patients (BEACON)

Обзор

This is a Phase I, open-label, multi-center study to assess the safety, pharmacokinetics, and preliminary efficacy of GPC3-directed chimeric antigen receptor modified T cells injection (Ori-C101) in Advanced Hepatocellular Carcinoma(HCC).

Вмешательства

• Биопрепарат Ori-C101
  Hepatic arterial infusion

Первичные конечные точки

• Maximum tolerated dose of Ori-C101 [Срок оценки: 1 year]

Вторичные конечные точки (1)

• Objective Response Rate [Срок оценки: 2 years]

Критерии участия

Критерии включения

• Confirmed pathologic or radiologic diagnosis of HCC ;
• Tumor tissue GPC3 expression positive by immunohistochemistry(IHC) at the local laboratory (Tumor samples ≤1 years prior to ICF signature are acceptable), if no archived tumor tissue samples, tumor biopsy is required for GPC3 expression test;
• Unresectable stage B (intermediate) or C (advanced) HCC according to the Barcelona Clinic Liver Cancer (BCLC) staging. If stage B, must have progressed after, or not be eligible for, surgical or locoregional therapy;
• Received at least two prior line of systemic therapy (included but not limited to target therapy, immunotherapy or chemotherapy) with radiologic disease progression during or following systemic therapy;
• Child-Pugh A or B7, no history of hepatic encephalopathy;
• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 at the time of ICF signature;
• Estimated life expectancy of minimum of 12 weeks;
• Must have at least 1 target lesion

Критерии исключения

• Central nervous system metastatic disease, leptomeningeal disease, or metastatic cord compression;
• Prior bone marrow or organ transplantation;
• Have a history of another primary malignancy within 5 years prior to starting study treatment. Exceptions here are as follows: the disease under study; adequately treated basal or squamous cell carcinoma of the skin; cancer of the cervix in situ;
• Active hepatitis B infection (If Hepatitis B surface antigen \[HBsAg\] or Hepatitis B core antibody \[HBcAb\] positive, then HBV-DNA must be < 20 IU/mL, and HBsAg-positive patients should have been treated with antiviral therapies as per the local guidelines);
• Positive hepatitis C (HCV) RNA, Human Immunodeficiency Virus (HIV) antibody, Cytomegalovirus(CMV) DNA or syphilis serology;
• Have received prior cell-based therapies such as targeted GPC3 therapy, TCR-T therapy, CAR-T therapy;
• Inadequate bone marrow reserve or organ function;
• History or current evidence of any condition or disease that could confound the results of the study or, in the opinion of Investigator, is not in the best interest of the patient to participate.
• Pregnant or Breast-feeding women.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Китай · 7 центров

• Peking University Cancer Hospital — Пекин
• Hunan Cancer Hospital — Чанша
• The first hospital of Jilin University — Changchun
• West China Hospital — Чэнду
• Sir Run Run Shaw Hospital — Ханчжоу
• Lishui Central Hospital — Lishui
• Zhongshan Hospital Fudan University — Шанхай

Идентификаторы

NCT: NCT05652920 · Ori-C101-P1

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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