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A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493 in Patients With Advanced or Refractory Solid Tumors or Lymphoma

2019年5月13日 更新者:Janssen Research & Development, LLC

A Phase 1 Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493, a Pan-Fibroblast Growth Factor Receptor (FGFR) Tyrosine Kinase Inhibitor, in Subjects With Advanced or Refractory Solid Tumors or Lymphoma

The purpose of this study is to determine a dose for future development and to evaluate the safety, pharmacokinetics, pharmacodynamics, and efficacy profiles of JNJ-42756493 in Japanese and other Asian patients with advanced or refractory solid tumors or lymphoma.

研究概览

详细说明

This is an open-label (identity of assigned study drug will be known), multicenter, 2-part, Phase 1 dose escalation/expansion to evaluate the safety, pharmacokinetics (study of what the body does to a drug), pharmacodynamics (study of what a drug does to the body) and clinical activity of JNJ-42756493 administered orally once daily in 21-day cycles or 28 days cycles of intermittent dosing regimen (7 days on/7 days off) to Japanese and Asian participants >=20 years of age with advanced or refractory solid tumors or lymphoma who are not candidates for approved or available therapies. Approximately 40 participants will be enrolled. In Part 1 Participants will be required to be hospitalized after the first dose on Day 1 of Cycle 1 until Day 2 of Cycle 2 (for daily continuous dosing) or until Day 14 of Cycle 1 (for intermittent dosing), however extension of hospitalization will be allowed until Day 2 of Cycle 2 according to investigators clinical judgment. The Part 1 dose-escalation phase is designed to determine the recommended Phase 2 dose (RP2D) based on safety, pharmacokinetic, and pharmacodynamic data of JNJ-42756493. Participants will be enrolled in sequential cohorts based on the 3+3 dose-escalation scheme; the first cohort will receive the starting dose and subsequent cohorts will receive increased doses of JNJ-42756493. After the last participants in each cohort completes Cycle 1, the Safety Evaluation Team (SET) will evaluate the safety and pharmacokinetic data according to protocol-defined criteria and make the decision whether to escalate the dose in a new cohort. To determine the recommended Phase 2 dose, the SET will review all safety, pharmacokinetic, and pharmacodynamic data from Part 1 before initiation of Part 2. The total number of participants enrolled in Part 1 will depend on the dose level at which the recommended Phase 2 dose is established. After the recommended Phase 2 dose is established, the Part 2 dose-expansion phase will be opened. Part 2 study will be done in a molecularly-defined subset of Participants with gastric adenocarcinoma including gastroesophageal junctions at the RP2D. In Part2, Participants can be hospitalized until Day 8 of Cycle 1 as needed. In addition, extension of hospitalization will be allowed until Day 15 of Cycle 1 according to investigator's clinical judgment. In Part 2, approximately 25 participants will be treated at the recommended Phase 2 dose as 28 days cycles of intermittent dosing regimen in order to evaluate fibroblast growth factor receptor target modulation in tumor, to further elaborate safety, pharmacokinetics, and pharmacodynamics of JNJ-42756493, as well as to evaluate preliminary clinical responses. Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent. Serial pharmacokinetic and pharmacodynamic samples will be collected, and safety and efficacy will be monitored throughout the study.

研究类型

介入性

注册 (实际的)

19

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。

学习地点

      • Kashiwa、日本
      • Matsuyama、日本
      • Tokyo、日本

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

20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:

  • Part 1: Histologically or cytologically confirmed solid malignancy or lymphoma that is metastatic or unresectable, and for which standard curative treatment is no longer effective
  • Part 2: Histologically or cytologically confirmed gastric adenocarcinoma including gastroesophageal junctions that is metastatic, locally advanced or unresectable, and for which standard treatment is no longer effective or tolerable
  • Eastern Cooperative Oncology Group performance status score 0 or 1
  • Adequate bone marrow, liver, and renal function according to protocol-defined criteria within the 7 days prior to Day 1 of Cycle 1
  • Laboratory values within protocol -defined parameters
  • Agrees to protocol-defined use of effective contraception
  • Negative urine pregnancy test (urine or serum beta human chorionic gonadotropin [beta-HCG]) at screening for women of child bearing potential

Exclusion Criteria:

  • Has had chemotherapy, radiotherapy, immunotherapy, or treatment with an investigational anticancer agent within 3 weeks (nitrosoureas and mitomycin C within 6 weeks) before the first administration of study drug (localized radiation therapy for palliative purposes and ongoing luteinizing hormone-releasing hormone agonists and antagonists for patients with prostate cancer, bisphosphonates and denosumab are permitted
  • History or current condition of uncontrolled cardiovascular disease as defined in the protocol
  • Taking medications known to have a risk of causing QTc prolongation and Torsades de Pointes or known as strong CYP3A inhibitors or inducers
  • Left ventricular ejection fraction less than (<) 50 percent (%) as assessed by echocardiography (or multi-gated acquisition [MUGA]) performed at screening
  • Uncontrolled intercurrent illness including, but not limited to, poorly controlled hypertension or diabetes, ongoing active infection, psychiatric illness, or a risk of gastrointestinal perforation

Woman who is pregnant, breast-feeding, or planning to become pregnant or is a man who plans to father a child, while the participant is enrolled in this study and is within 3 or 5 months, respectively, after the last dose of the study drug

  • Not recovered from reversible, clinically significant toxicity of prior anticancer therapy
  • Presence of any medical condition that requires intact wound healing capacity and is expected to endanger participant safety if wound healing capacity would be severely reduced during administration of the investigational agent
  • Major surgery within 4 weeks before enrollment
  • Known human immunodeficiency virus infection
  • Known hepatitis B or C (except hepatocellular carcinoma)
  • Active, symptomatic, or untreated brain metastasis

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:非随机化
  • 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:Part 1: Dose Escalation (Daily Dosing)
Dose escalation of JNJ-42756493 is to occur until a dose at which <33 percent of participants experience a dose-limiting toxicity, the maximum concentration of JNJ-42756493 is less than the protocol-defined cardiovascular threshold, and JNJ-42756493 is biologically active. Participants will receive study drug once day on Day 1 of Cycle 1 followed by a 2-day drug-free period (Days 2 and 3 of Cycle 1) and continues throughout the 21 day cycle. For all subsequent cycles once a day for 21 days.
JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
实验性的:Part 1: Dose Escalation (Intermittent Dosing)
Intermitting dosing regimen will be 28 days (7 days on and 7 days off). Participants will receive JNJ-42756493 on Days 1 to 7 and Days 15 to 21 of each cycle; JNJ-42756493 will not be administered on Days 8 to 14 and Days 22 to 28 of each cycle.
JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
实验性的:Part 2: Dose Expansion
Participants will receive the recommended Phase 2 JNJ-42756493 dose determined in Part 1 as Intermitting dosing regimen (28 days, 7 days on and 7 days off). Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent.
Recommended Phase 2 JNJ-42756493 dose determined in Part 1 administered orally for 28-days cycles (Intermitting dosing regimen).

研究衡量的是什么?

主要结果指标

结果测量
大体时间
按 MedDRA 系统器官分类 (SOC) 和首选术语 (PT) 划分的受不良事件影响的参与者人数
大体时间:最后一次研究药物给药后最多 30 天
最后一次研究药物给药后最多 30 天

次要结果测量

结果测量
大体时间
Maximum observed plasma concentration of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Minimum observed plasma concentration of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Time correspondent to the maximum observed plasma concentration of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Area under the plasma concentration-time curve from time 0 to 24 hours of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Half-life of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Apparent volume of distribution of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Total clearance of drug of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Accumulation index of JNJ-42756493
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
Number of participants with complete response
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Number of participants with partial response
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Number of participants with stable disease
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Number of participants with progressive disease
大体时间:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2013年8月21日

初级完成 (实际的)

2016年1月28日

研究完成 (实际的)

2016年1月28日

研究注册日期

首次提交

2013年7月26日

首先提交符合 QC 标准的

2013年10月10日

首次发布 (估计)

2013年10月14日

研究记录更新

最后更新发布 (实际的)

2019年5月15日

上次提交的符合 QC 标准的更新

2019年5月13日

最后验证

2019年5月1日

更多信息

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.

Part 1: JNJ-42756493的临床试验

3
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