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PDR001 in Patients With Non-small Cell Lung Cancer Harboring KRAS/NRAS Mutation or no Actionable Genetic Abnormalities

2018年10月1日 更新者:Sang-We Kim、Asan Medical Center

An Open-label, Multicenter, Phase II Study of PDR001 in Patients With Non-small Cell Lung Cancer Harboring KRAS/NRAS Mutation or Without Actionable Genetic Abnormalities, Detected Using NGS Platform

This study is a phase II, single-arm, open label study. All participating patients must sign on the written informed consent form, and a separate form of consent will be used for the use of tissue for the biomarker research.

研究概览

地位

未知

干预/治疗

详细说明

This clinical study is targeted for the patients who harbor KRAS/NRAS mutation or no actionable genetic abnormalities detected using NGS platform and all patients will be treated with PDR001. The treatment period begins on Day 1 of Cycle 1 and 1 cycle consists of 21 days.

Patients will be continued to receive study drug until the end of study unless the patients in disease progression, unacceptable toxicity, withdrawn consent, or by the investigator's judgment.

The progression of the disease in most patients is defined radiographically and determined according to RECIST criteria ver. 1.1. If there are patients those who need to be provided investigational drug beyond predefined end of treatment, additional extended providing of PDR001 needs the mutual agreement of the investigators and Novartis followed by amendment of study protocol and contract.

At the investigator's discretion, patients who have the initial RECIST PD may continue PDR001. At any time, if assessed by the investigator that the patient is no longer benefiting from PDR001, or the patient experiences a second PD by RECIST, then the patient shall come off study medication.

研究类型

介入性

注册 (预期的)

70

阶段

  • 阶段2

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。

学习地点

      • Seoul、大韩民国、05505
        • 招聘中
        • Asan Medical Center
        • 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

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Subjects with histologically or cytologically confirmed, stage IV or recurrent NSCLC that carries a KRAS/NRAS mutation or no actionable mutation, which are identified by NGS.
  • Squamous cell carcinoma and non-squamous cell carcinoma will be enrolled with 1:1 ratio for efficacy analysis according to histology
  • Subjects who did not treated with prior anti-PD-1 antibody nor anti-PD-L1 antibodies
  • ECOG performance status of 0 to 2
  • Male or female; ≥ 18 years of age
  • Patients those who showed disease progression after one or two prior platinum-containing regimen
  • Patients who have received prior platinum-containing adjuvant, neoadjuvant, or definitive chemoradiation for locally advanced disease are eligible, provided that progression has occurred ≥ 12 months from last therapy.
  • Subjects with at least one measurable lesion (using RECIST 1.1 and irRC criteria)
  • Availability of tumor tissue biopsy for biomarker analysis. Archival tissue can be used. Fine-needle aspirates will not be acceptable.
  • Subjects who meet the following criteria:
  • Absolute neutrophil count (ANC) ≥ 1.5 x 109/L
  • Platelet count ≥100 x 10^9/L
  • Serum creatinine ≥ 1.5 x upper limit of normal (ULN)
  • AST (SGOT) and ALT (SGPT) ≥ 3 x upper limit of normal (ULN) (If there is Liver Metastasis ≥ 5 x upper limit of normal (ULN))
  • Total bilirubin≥1.5 x upper limit of normal (ULN)
  • Life expectancy of ≥ 12 weeks on C1D1
  • Provision of written informed consent prior to any study specific procedures

Exclusion Criteria:

  • Patients who harboring EGFR mutation(s) and/or anaplastic lymphoma kinase (ALK) rearrangement will not be eligible for this trial.
  • Patients who have received more than 3 lines of prior systemic therapy, including cytotoxic agent or targeted agent
  • Previous treatment with immune oncologic agents
  • Any major operation or irradiation within 4 weeks of baseline disease assessment
  • Subjects with symptomatic central nervous system (CNS) metastases who are neurologically unstable or have required increasing doses of steroids within the 2 weeks prior to study entry to manage CNS symptoms
  • Subjects with history of leptomeningeal metastasis
  • Other co-existing malignancies or malignancies diagnosed within the last 3 years with the exception of basal cell carcinoma or cervical cancer in situ. Any cured cancer that is considered to have no impact in PFS and OS for the current NSCLC such as thyroid cancer.
  • Subjects with an uncontrolled major cardiovascular disease (including AMI within 12 months, unstable angina within 6 months, over NYHA class III congestive heart failure, congenital long QT syndrome (Corrected QT (QTcF) >470 ms using Fridericia's correction on the screening ECG), 2° or more AV Block and uncontrolled hypertension)
  • Pregnant or lactating female
  • Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the study
  • History of severe hypersensitivity reactions to other monoclonal antibodies, which in the opinion of the investigator may pose an increased risk of serious infusion reaction.
  • Active, known or suspected autoimmune disease or a documented history of autoimmune disease, including ulcerative colitis and Crohn's disease (Patients with vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger are permitted to enroll).
  • Patient has history of interstitial lung disease or interstitial pneumonitis, including clinically significant radiation pneumonitis (i.e., affecting activities of daily living or requiring therapeutic intervention).
  • Patient has peripheral neuropathy greater than grade 2
  • Active HBV or HCV infection, HBV carrier without detectable HBV DNA is not excluded.
  • Known history of testing positive for Human Immunodeficiency Virus (HIV) infection
  • Any medical condition that would, in the investigator's judgment, prevent the patient's participation in the clinical study due to safety concerns, compliance with clinical study procedures or interpretation of study results.
  • Patients requiring chronic treatment with systemic steroid therapy or any immunosuppressive therapy, other than replacement-dose steroids in the setting of adrenal insufficiency. Topical, inhaled, nasal and ophthalmic steoids are not prohibited.
  • Use of any live vaccines against infectious disease within 4 weeks of initiation of study treatment.
  • Women of child-bearing potential, unless they are using highly effective methods of contraception during dosing and for 150 days after the last dose of study treatment.
  • Sexually active males unless they use a condom during treatment and for 150 days after stopping study treatment .

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:PDR001
PDR001 300 mg (fixed dose) intraveneously every 3 weeks
PDR001 300 mg (fixed dose) intraveneously every 3 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
客观反应率
大体时间:在第 6 周,然后每 6 周一次,直到第 36 周。然后每 12 周一次,直到出院,平均 13.8 个月]
ORR 是具有最佳总体反应的患者比例,由 RECIST1.1 定义为完全反应或部分反应
在第 6 周,然后每 6 周一次,直到第 36 周。然后每 12 周一次,直到出院,平均 13.8 个月]

次要结果测量

结果测量
措施说明
大体时间
无进展生存期
大体时间:在第 6 周,然后每 6 周一次,直到第 36 周。然后每 12 周一次,直到出院,平均 13.8 个月

PFS 被定义为从第一剂研究产品 (IPs) 到疾病进展或因任何原因死亡的时间。

OS 定义为从 IP 的第一剂到由于任何原因死亡的时间。

在第 6 周,然后每 6 周一次,直到第 36 周。然后每 12 周一次,直到出院,平均 13.8 个月
总生存期
大体时间:在第 6 周,然后每 6 周一次,直到第 36 周。然后每 12 周一次,直到出院,平均 13.8 个月
在第 6 周,然后每 6 周一次,直到第 36 周。然后每 12 周一次,直到出院,平均 13.8 个月
Disease control rate
大体时间:At Week 6 then every 6 weeks up to Week 36.and then every 12 weeks until discharge, for an average of 13.8 months
DCR is calculated as the proportion of patients with best response of CR, PR and SD.
At Week 6 then every 6 weeks up to Week 36.and then every 12 weeks until discharge, for an average of 13.8 months
Duration of response
大体时间:At Week 6 then every 6 weeks up to Week 36.and then every 12 weeks until discharge, for an average of 13.8 months]
DOR is calculated as the time from the date of the first document of complete remission (CR) or partial remission (PR) to the first documented preogressive disease (PD) or death due to any cause for patients with PR or CR.
At Week 6 then every 6 weeks up to Week 36.and then every 12 weeks until discharge, for an average of 13.8 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 (预期的)

2018年11月1日

初级完成 (预期的)

2020年6月30日

研究完成 (预期的)

2022年6月30日

研究注册日期

首次提交

2018年10月1日

首先提交符合 QC 标准的

2018年10月1日

首次发布 (实际的)

2018年10月3日

研究记录更新

最后更新发布 (实际的)

2018年10月3日

上次提交的符合 QC 标准的更新

2018年10月1日

最后验证

2018年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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.

PDR001的临床试验

3
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