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A Study of Ipatasertib in Participants With Mild, Moderate or Severe Hepatic Impairment Compared to Healthy Participants

2019年11月15日 更新者:Genentech, Inc.

A Phase 1, Open-Label, Single-Dose Study to Evaluate the Pharmacokinetics and Safety of Ipatasertib in Subjects With Mild, Moderate or Severe Hepatic Impairment Compared to Healthy Subjects

This is a Phase 1 study evaluating the pharmacokinetics, tolerability and safety of a single dose of ipatasertib in participants with mild, moderate or severe hepatic impairment compared to healthy participants.

研究概览

地位

完全的

研究类型

介入性

注册 (实际的)

29

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

    • Florida
      • Miami、Florida、美国、33014
        • Clinical Pharmacology of Miami, Inc.
    • Tennessee
      • Knoxville、Tennessee、美国、37920
        • New Orleans Center for Clinical Research
    • Texas
      • San Antonio、Texas、美国、78215
        • American Research Corporation Inc.

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 至 74年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • In good health (except for specific inclusion criteria related to hepatic impairment), as determined by the Investigator, based on no clinically significant findings from medical history, physical examination, 12-lead electrocardiogram, and vital signs
  • Females will not be pregnant or breastfeeding, and must be either postmenopausal or agree to use a study-approved method of contraception from the time of signing the informed consent until 30 days after discharge
  • Males will either be sterile or agree to use male condom with spermicide from check-in (Day -1) until 90 days following the dose of study drug

Additional Inclusion Criteria for Healthy Subjects Only:

- Liver enzyme tests must be less than or equal to the upper limits of normal

Additional Exclusion Criteria for Hepatic Impaired Subjects Only:

- Hepatic impairment must have a Child-Pugh score of 5 to 6 (mild), 7 to 9 (moderate), or 10 to 15 (severe) and have stable hepatic insufficiency within 1 month prior to Screening

Exclusion Criteria:

  • History of ulcerative colitis or stomach or intestinal surgery or resection
  • History of unstable diabetes mellitus
  • History of alcoholism or drug addiction within 1 year prior to Check-in (Day -1)
  • Use of oral, implantable, transdermal, or injectable contraceptives from the time of signing the informed consent (females only) or 10 days prior to Check-in through 45 days after the dose administration
  • Poor peripheral venous access
  • Receipt of blood products within 2 months prior to check-in

Additional Exclusion Criteria for Healthy Subjects Only:

  • Use of any tobacco- or nicotine-containing products within 6 months prior to check-in and during the entire study
  • Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, or psychiatric disorder

Additional Exclusion Criteria for Hepatic Impaired Subjects Only:

  • Any evidence of progressive liver disease that has worsened or is worsening within 1 month prior to the screening visit
  • Participant has shown evidence of hepatorenal syndrome
  • Ascites requiring paracentesis
  • Participant has required treatment for GI bleeding within 12 months prior to Check-in
  • Participant has required additional medication for hepatic encephalopathy within the 12 months (6 months for severe hepatic impairment) prior to check-in
  • Total bilirubin levels >6 mg/dL

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:Normal Hepatic Function
Participants with normal hepatic function will be administered a single oral dose of ipatasertib (100 mg).
A single oral dose of 100 mg ipatasertib will be administered.
其他名称:
  • GDC-0068
实验性的:Mild Hepatic Impairment
Participants with mild hepatic impairment (Child-Pugh Class A, score of 5 to 6, inclusive) will be administered a single dose of ipatasertib (100 mg).
A single oral dose of 100 mg ipatasertib will be administered.
其他名称:
  • GDC-0068
实验性的:Moderate Hepatic Impairment
Participants with moderate hepatic impairment (Child-Pugh Class B, score of 7 to 9, inclusive) will be administered a single dose of ipatasertib (100 mg).
A single oral dose of 100 mg ipatasertib will be administered.
其他名称:
  • GDC-0068
实验性的:Severe Hepatic Impairment
Participants with severe hepatic impairment (Child-Pugh Class C, score of 10 to 15, inclusive) will be administered a single dose of ipatasertib (100 mg).
A single oral dose of 100 mg ipatasertib will be administered.
其他名称:
  • GDC-0068

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
Area Under the Plasma Concentration-Time Curve (AUC) from 0 to Infinity (AUC0-inf) of Ipatasertib
大体时间:up to Day 15
AUC0-inf is defined as AUC extrapolated from Hour 0 to infinity of ipatasertib in the plasma.
up to Day 15
Maximum Observed Plasma Concentration (Cmax) of Ipatasertib
大体时间:up to Day 15
Maximum observed concentration of ipatasertib as determined by measuring drug concentration in blood samples over time.
up to Day 15

次要结果测量

结果测量
措施说明
大体时间
Percentage of Participants with Treatment-Emergent Adverse Events (AE)
大体时间:up to Day 15
An AE is any untoward medical occurrence in a participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with the treatment. An adverse event can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a pharmaceutical product, whether or not considered related to the pharmaceutical product. Preexisting conditions which worsen during a study are also considered as adverse events.
up to Day 15
Time to Reach Maximum Observed Concentration (tmax) of Ipatasertib
大体时间:up to Day 15
Time from dose administration to observed maximum serum concentration for ipatasertib as determined by measuring drug concentration in blood samples over time.
up to Day 15
AUC from 0 to last measurable concentration (AUC0-t)
大体时间:up to Day 15
Area under the plasma concentration-time curve from Hour 0 to the last measurable concentration of ipatasertib.
up to Day 15
Half-life (t1/2) of Ipatasertib
大体时间:up to Day 15
Half-life of ipatasertib is the time elapsed for the drug concentration to decrease by half as determined by measuring drug concentration in blood samples over time.
up to Day 15
Apparent Plasma Clearance (CL/F) of Ipatasertib
大体时间:Up to Day 15
Apparent clearance (CL/F) of ipatasertib, where CL is clearance and F is bioavailability (relative amount of extravascularly-administered drug that reaches systemic circulation unchanged). Determined by measuring drug concentration in blood samples over time.
Up to Day 15
Apparent Volume of Distribution (V/F) of Ipatasertib
大体时间:up to Day 15
Apparent volume of distribution (V/F) during the terminal phase of ipatasertib.
up to Day 15

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)

2017年11月9日

初级完成 (实际的)

2018年6月26日

研究完成 (实际的)

2018年6月26日

研究注册日期

首次提交

2017年11月9日

首先提交符合 QC 标准的

2017年11月9日

首次发布 (实际的)

2017年11月14日

研究记录更新

最后更新发布 (实际的)

2019年11月18日

上次提交的符合 QC 标准的更新

2019年11月15日

最后验证

2019年11月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • GP40200

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

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