An Open-label, Single-arm Phase 2 Study of ES014 in Subjects With Advanced Solid Tumors
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Evaluating the Efficacy of ES014 in Adult Subjects with Advanced Solid Tumours
研究概览
简要总结
OVERALL DESIGN: This study is an open-label, single-center, single-arm phase 2 clinical study designed to evaluate the efficacy, safety, and tolerability of ES014 in adults with advanced solid tumors. Adult patients with unresectable locally advanced or metastatic solid tumors will be enrolled in this study. This study is not blinded.
Subject type and number : The study population will be adults with unresectable locally advanced or metastatic solid tumors, whose disease has progressed despite standard therapy and for whom no further standard therapy exists; or for whom standard therapy has proven to be ineffective or intolerable.
This study is expected to enroll no more than 15 subjects, including malignant pleural mesothelioma and myxofibrosarcoma, 4-5, respectively, 2-3 malignant peripheral nerve sheath tumors, and other solid tumors.
Duration of treatment: Subjects will be treated with ES014 in 28-day cycles. ES014 will be administered at 1400 mg on days 1 and 15 of each cycle. Each subject will be treated with study drug for a maximum of 24 months. Subjects will be treated according to protocol until disease progression per RECIST v1.1, development of unacceptable toxicity, withdrawal of consent, completion of study treatment of 24 months, end of study, or early termination of study by sponsor, or other discontinuation and withdrawal reason, whichever occurs first.
详细描述
Subject type and number : The study population will be adults with unresectable locally advanced or metastatic solid tumors, whose disease has progressed despite standard therapy and for whom no further standard therapy exists; or for whom standard therapy has proven to be ineffective or intolerable.
- Cohort A: malignant pleural mesothelioma
- Cohort B: Mucinous fibrosarcoma
- Cohort C: Malignant peripheral nerve sheath tumour
- Cohort D: Other solid tumours
This study is expected to enroll no more than 15 subjects, including malignant pleural mesothelioma and myxofibrosarcoma, 4-5, respectively, 2-3 malignant peripheral nerve sheath tumors, and other solid tumors.
Duration of treatment: Subjects will be treated with ES014 in 28-day cycles. ES014 will be administered at 1400 mg on days 1 and 15 of each cycle. Each subject will be treated with study drug for a maximum of 24 months. Subjects will be treated according to protocol until disease progression per RECIST v1.1, development of unacceptable toxicity, withdrawal of consent, completion of study treatment of 24 months, end of study, or early termination of study by sponsor, or other discontinuation and withdrawal reason, whichever occurs first.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histological or cytological documentation of unresectable locally advanced or metastatic solid tumours.
- •Presence of at least one measurable lesion (according to RECIST v1.1).
- •Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or
- •Life expectancy of at least 12 weeks.
- •Adequate hematologic, hepatic, renal and coagulation functions per protocol.
排除标准
- •Any prior therapy targeting CD39, CD73, adenosine A2A receptor, or TGF-β.
- •Receipt of any investigational agents or devices within 4 weeks prior to the first dose of study drug.
- •Prior treatment with the following therapies:
- •Anticancer therapy within 28 days or 5 half-lives of the drug prior to the first dose of study drug, whichever is shorter. At least 14 days must have elapsed between the last dose of prior anticancer agent and the first dose of study drug is administered with certain exceptions. A wash out of at least 2 weeks before the start of study drug for radiation to the extremities and 4 weeks for radiation to the chest, brain, or visceral organs is required.
- •Prior allogeneic or autologous bone marrow transplant or solid organ transplant.
- •Subject has received an infusion of blood products (including platelets or red blood cells), granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), recombinant erythropoietin, or recombinant thrombopoietin within 14 days prior to the first administration of study treatment.
研究组 & 干预措施
ES014
ES014 will be administered in patients with advanced solid tumors.
干预措施: ES014 (Drug)
结局指标
主要结局
Evaluating the Efficacy of ES014 in Adult Subjects with Advanced Solid Tumours
时间窗: 1-2 years
ORR assessed by the investigators according to RECIST v1.1
次要结局
未报告次要终点