此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

A Study of BL-ARC002 in Patients With Locally Advanced or Metastatic Solid Tumors

2026年8月25日 更新者:Sichuan Baili Pharmaceutical Co., Ltd.

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy of BL-ARC002 for Injection in Patients With Locally Advanced or Metastatic Solid Tumors

This study is an open-label, multicenter, dose-escalation and expansion, non-randomized Phase I clinical study to evaluate the safety, tolerability, pharmacokinetic characteristics, and preliminary efficacy of BL-ARC002 for injection in patients with locally advanced or metastatic solid tumors.

研究概览

地位

招聘中

条件

干预/治疗

详细说明

The study consists of two phases: a dose-escalation phase (Phase Ia) and an expansion phase (Phase Ib).

研究类型

介入性

注册 (估计的)

22

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Tianjin Municipality
      • Tianjin、Tianjin Municipality、中国
        • 招聘中
        • Tianjin Cancer Hospital
        • 接触:
          • Jihui Hao

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Voluntarily sign the informed consent form and comply with the protocol requirements;
  2. No gender restrictions;
  3. Age: ≥18 and ≤75 years (Phase Ia); ≥18 years (Phase Ib);
  4. Expected survival time ≥3 months;
  5. Histopathologically and/or cytologically confirmed locally advanced or metastatic solid tumors that have failed standard treatment;
  6. Agree to provide archived tumor tissue specimens or fresh tissue samples from the primary or metastatic lesions within the past 2 years;
  7. Must have at least one measurable lesion as defined by RECIST v1.1;
  8. Eastern Cooperative Oncology Group performance status of 0 or 1;
  9. Toxicities from prior anti-tumor therapy must have recovered to ≤ Grade 1 as defined by NCI-CTCAE v5.0;
  10. No severe cardiac dysfunction, with left ventricular ejection fraction ≥50%;
  11. Organ function levels must meet the required criteria;
  12. Coagulation function: International normalized ratio ≤1.5 and activated partial thromboplastin time ≤1.5 × upper limit of normal;
  13. Urine protein ≤2+ or ≤1000 mg/24 hours;
  14. For premenopausal women of childbearing potential, a pregnancy test must be performed within 7 days before starting treatment, with serum pregnancy test being negative, and they must not be breastfeeding; all enrolled patients (regardless of sex) must practice adequate barrier contraception throughout the entire treatment period and for 6 months after treatment completion.

Exclusion Criteria:

  1. Use of chemotherapy, biotherapy, immunotherapy, etc., within 4 weeks or 5 half-lives prior to the first dose;
  2. History of serious heart disease;
  3. QT interval prolongation, complete left bundle branch block, or third-degree atrioventricular block;
  4. Active autoimmune diseases and inflammatory diseases;
  5. Diagnosis of another malignancy within 5 years prior to the first dose;
  6. Hypertension inadequately controlled by two antihypertensive medications;
  7. History of ILD requiring steroid therapy, current ILD, or ≥ Grade 2 radiation pneumonitis;
  8. Active symptoms of central nervous system metastasis;
  9. History of allergy to recombinant humanized or human-mouse chimeric antibodies, or allergy to any excipient component of BL-ARC002;
  10. Prior organ transplantation or allogeneic hematopoietic stem cell transplantation;
  11. Cumulative anthracycline dose > 360 mg/m² from prior (neo)adjuvant anthracycline-based therapy;
  12. Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
  13. Active infection requiring systemic therapy;
  14. Participation in another clinical trial within 4 weeks prior to the first dose;
  15. Pregnancy or breastfeeding;
  16. Study participants with claustrophobia or any condition preventing them from lying still to complete examinations;
  17. Other conditions deemed by the investigator to make the participant unsuitable for this clinical trial.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:BL-ARC002
Participants receive BL-ARC002 for the first cycle (6 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
Administration by intravenous infusion for a cycle of 6 weeks.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Ia期:剂量限制性毒性(DLT)
大体时间:首剂接种后最多42天
DLT依据NCI-CTCAE v5.0标准在第一周期内进行评估,若研究者判定其可能、很可能或确定与研究药物给药相关,则定义为DLT定义中任何毒性的发生。
首剂接种后最多42天
Ia期:最大耐受剂量(MTD)
大体时间:首剂接种后最多42天
MTD被定义为在第一个治疗周期内,不超过六分之一的受试者发生剂量限制性毒性(DLT)的最高剂量水平。
首剂接种后最多42天
Phase Ib: Recommended Phase II Dose (RP2D)
大体时间:Up to approximately 24 months
The RP2D is defined as the dose level chosen by the sponsor (in consultation with the investigators) for phase II study, based on safety, tolerability, efficacy, PK, and PD data collected during the dose escalation study of BL-ARC002.
Up to approximately 24 months

次要结果测量

结果测量
措施说明
大体时间
AUC0-t
大体时间:最长约 24 个月
AUC0-t 定义为从时间 0 到最后可测量浓度的时间的血清浓度-时间曲线下的面积。
最长约 24 个月
Ib 期:客观缓解率 (ORR)
大体时间:最长约 24 个月
ORR 定义为达到 CR(所有目标病灶消失)或 PR(目标病灶直径总和至少减少 30%)的参与者百分比。 经历确认的 CR 或 PR 的参与者的百分比根据 RECIST 1.1 计算。
最长约 24 个月
Ib 阶段:疾病控制率 (DCR)
大体时间:最长约 24 个月
DCR 定义为患有 CR、PR 或稳定疾病的参与者的百分比(SD:既没有足够的收缩来符合 PR 的条件,也没有足够的增加来符合进行性疾病的条件 [PD:至少增加 20% 的总和目标病灶的直径绝对增加至少 5 毫米。 出现一个或多个新病变也被认为是 PD])。
最长约 24 个月
Ib 阶段:反应持续时间 (DOR)
大体时间:最长约 24 个月
应答者的 DOR 定义为从参与者最初客观应答到疾病进展或死亡(以先发生者为准)的第一个日期的时间。
最长约 24 个月
Treatment-Emergent Adverse Event (TEAE)
大体时间:Up to approximately 24 months
TEAE is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally emerging, or any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a pre-existing condition during the treatment of BL-ARC002. The type, frequency and severity of TEAE will be evaluated during the treatment of BL-ARC002.
Up to approximately 24 months
Cmax
大体时间:Up to approximately 24 months
Maximum serum concentration (Cmax) of BL-ARC002 will be investigated.
Up to approximately 24 months
Tmax
大体时间:Up to approximately 24 months
Time to maximum serum concentration (Tmax) of BL-ARC002 will be investigated.
Up to approximately 24 months
T1/2
大体时间:Up to approximately 24 months
Half-life (T1/2) of BL-ARC002 will be investigated.
Up to approximately 24 months
CL (Clearance)
大体时间:Up to approximately 24 months
CL in the serum of BL-ARC002 per unit of time will be investigated.
Up to approximately 24 months
Ctrough
大体时间:Up to approximately 24 months
Ctrough is defined as the lowest serum concentration of BL-ARC002 prior to the next dose will be administered.
Up to approximately 24 months
ADA (anti-drug antibody)
大体时间:Up to approximately 24 months
Frequency of anti-BL-ARC002 antibody (ADA) will be investigated.
Up to approximately 24 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年5月13日

初级完成 (估计的)

2027年12月1日

研究完成 (估计的)

2027年12月1日

研究注册日期

首次提交

2026年5月9日

首先提交符合 QC 标准的

2026年5月9日

首次发布 (实际的)

2026年5月15日

研究记录更新

最后更新发布 (实际的)

2026年8月27日

上次提交的符合 QC 标准的更新

2026年8月25日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • BL-ARC002-101

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅