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A Study of AK138D1 Alone or in Combination With Ivonescimab in Advanced Non-Small Cell Lung Cancer

2026年7月28日 更新者:Akeso

A Phase Ib/II Study of AK138D1 as Monotherapy and in Combination With Ivonescimab in Patients With Advanced Non-Small Cell Lung Cancer

The goal of this clinical trial is to evaluate the safety, tolerability, and efficacy of AK138D1 as monotherapy or in combination with ivonescimab in patients with advanced non-small cell lung cancer.

Participants will receive study treatment with AK138D1 alone or in combination with ivonescimab, undergo safety assessments and tumor evaluations, and be followed for treatment tolerability, antitumor activity, and clinical outcomes.

研究概览

详细说明

This is a multicenter, open-label phase Ib/II study of AK138D1 as monotherapy or in combination with ivonescimab in patients with advanced non-small cell lung cancer. The phase Ib portion is designed to evaluate the safety, tolerability, and preliminary antitumor activity of AK138D1 in combination with ivonescimab. The phase II portion is designed to evaluate the safety and efficacy of AK138D1 as monotherapy or in combination with ivonescimab.

研究类型

介入性

注册 (估计的)

265

阶段

  • 阶段2
  • 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

    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国
        • 招聘中
        • Shanghai East Hospital
        • 接触:

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. The subject must sign the written informed consent form (ICF) voluntarily;
  2. At enrollment, aged ≥ 18 to ≤ 75 years, both males and females are eligible;
  3. Has an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1;
  4. Has a life expectancy of ≥ 3 months;
  5. Has measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
  6. Has Stage IIIB/IIIC or IV non-small cell lung cancer (NSCLC) (American Joint Committee on Cancer [AJCC]).
  7. Adequate organ function.

Exclusion Criteria:

  1. Concomitant participation in another clinical study, unless it is a non-interventional clinical study or the follow-up period of an interventional study;
  2. Presence of active central nervous system (CNS) metastases.
  3. Live vaccines or attenuated live vaccines administered within 4 weeks prior to the first dose, or planned to be administered during the study; use of inactivated vaccines is allowed;
  4. Untreated subjects with active hepatitis B or active hepatitis C;
  5. Known active pulmonary tuberculosis (TB); subjects with suspected active TB must undergo appropriate clinical assessment to rule out the presence of active disease;
  6. Known active syphilis infection;
  7. Subjects with known allergy to any component of any study drug; and with a history of known severe hypersensitivity reactions to other monoclonal antibodies;
  8. Other reasons for ineligibility as evaluated by investigator.

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:随机化
  • 介入模型:并行分配
  • 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:AK138D1
AK138D1 will be administered at pre-specified dose levels.
登记的受试者将根据其队列中指定的给药方案接受 AK138D1 静脉输注 (IV)。
实验性的:AK138D1+ Ivonescimab
AK138D1 and ivonescimab will be administered at pre-specified dose levels.
登记的受试者将根据其队列中指定的给药方案接受 AK138D1 静脉输注 (IV)。
Enrolled subjects will receive intravenous infusion (IV) of Ivonescimab according to the dosing regimen specified in their cohort.
实验性的:AK138D1 + Ivonescimab + Carboplatin
AK138D1, ivonescimab and carboplatin will be administered at pre-specified dose levels.
登记的受试者将根据其队列中指定的给药方案接受 AK138D1 静脉输注 (IV)。
Enrolled subjects will receive intravenous infusion (IV) of Ivonescimab according to the dosing regimen specified in their cohort.
Enrolled subjects will receive intravenous infusion (IV) of Carboplatin according to the dosing regimen specified in their cohort.

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
Adverse events (AEs)
大体时间:Up to approximately 2 years
Incidence and severity of subjects with adverse events
Up to approximately 2 years
Objective Response Rate (ORR)
大体时间:Up to approximately 2 years
Objective Response Rate (ORR) is the proportion of subjects with complete response (CR) or partial response (PR) , assessed by investigator according to RECIST v1.1.
Up to approximately 2 years

次要结果测量

结果测量
措施说明
大体时间
抗药物抗体(ADA)
大体时间:最长约 2 年
可检测到抗药物抗体 (ADA) 的受试者数量。
最长约 2 年
总生存期 (OS)
大体时间:最长约 2 年
总生存期(OS)定义为从随机分组到因任何原因死亡的时间。
最长约 2 年
Disease Control Rate (DCR)
大体时间:Up to approximately 2 years
Disease control rate (DCR) assessed by investigator according to RECIST v1.1.
Up to approximately 2 years
Duration of response (DoR)
大体时间:Up to approximately 2 years
Duration of response (DoR) assessed by investigator according to RECIST v1.1.
Up to approximately 2 years
Time to response (TTR)
大体时间:Up to approximately 2 years
Time to response (TTR) is defined as the time to response assessed by investigator according to RECIST v1.1.
Up to approximately 2 years
Pharmacokinetics (PK) characteristics
大体时间:Up to approximately 2 years
Serum drug concentration profiles at different time points after administration.
Up to approximately 2 years
Progression Free Survival (PFS)
大体时间:Up to approximately 2 years
Progression Free Survival (PFS) is defined as the time from randomization to the first documented disease progression (per RECIST v1.1) assessed by investigator or death due to any cause, whichever occurs first.
Up to approximately 2 years

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。

赞助

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7月7日

初级完成 (估计的)

2028年6月18日

研究完成 (估计的)

2030年7月3日

研究注册日期

首次提交

2026年5月28日

首先提交符合 QC 标准的

2026年5月28日

首次发布 (实际的)

2026年6月3日

研究记录更新

最后更新发布 (实际的)

2026年7月29日

上次提交的符合 QC 标准的更新

2026年7月28日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

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.

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