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 24-wk Dose Ranging Study to Evaluate the Efficacy and Safety of 4 Doses of a New PDE4 Inhibitor in Patients With COPD (PIONEER)

2019年1月25日 更新者:Chiesi Farmaceutici S.p.A.

A 24-week, Multicenter, Randomized, Double-blind, Double-dummy, Placebo and Active Controlled, Parallel Group, Dose Ranging Study to Evaluate the Efficacy and Safety of 4 Doses of CHF6001 DPI in Patients With COPD on a Background Therapy

The purpose of this study is to evaluate the dose-response relationship of different doses of CHF6001 and to identify the optimal dose (s) in terms of benefit/risk ratio for further development in the target patient population.

研究概览

详细说明

This is a phase II, randomized, double-blind, double-dummy, placebo and active controlled multinational, multicenter, dose ranging, 6-arm parallel-group study to identify the optimal dose of CHF6001, PDE4 inhibitor under development, with respect to lung functions and symptoms.

After a 2-wk run-in period under formoterol (Oxis Turbohaler®) and rescue salbutamol prn, patients will be randomized to one of the 6 treatment groups. After the randomization, patients will be assessed after 3, 6, 12, 18 and 24 weeks of treatment at clinic/hospital. A follow-up visit will be performed 12 days after the last visit.

During the study, patients will report daily symptoms with the EXACT-PRO/E-RS questionnaire, rescue/background medication use and compliance with the study medications. AEs, SAEs and COPD exacerbations will be monitored throughout the study. At randomization and subsequent visits, patients will undergo physical and vital signs examinations, spirometry measurement, 12-lead ECG. Symptoms and Health status will be assessed through validated questionnaires. Routine lab analysis and blood biomarkers will be done.

研究类型

介入性

注册 (实际的)

1130

阶段

  • 阶段2

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

40年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • COPD patients
  • Non- childbearing potential or woman permanently sterilized or on one or more highly effective contraception
  • Current/ex smokers (history > 10 pack years)
  • Post bronchodilatator FEV1 >=30% and <=70% predicted normal value and FEV1/FVC ratio <0.7
  • Documented history of at least 1 moderate or severe exacerbation in the 12 months prior to study entry
  • Symptomatic patients (MMRC score ≥2 and a CAT score ≥10)
  • Patients on daily maintenance therapy with an ICS/LABA .

Exclusion Criteria:

  • Diagnosis of asthma or other respiratory disorders
  • Maintenance bronchodilators therapy only (eg LABA alone)
  • Maintenance triple therapy.
  • Occurrence of a moderate or severe COPD exacerbation within 6 weeks prior to study entry or during the run-in period.
  • Patients requiring long term oxygen therapy.
  • Concomitant or recent pulmonary rehabilitation programme
  • Known respiratory disorders other than COPD
  • Lung cancer or a history of lung cancer, active or history of cancer with less than 5 years disease free survival time
  • Hypersensitivity to β2-agonist, corticosteroids, PDE4 inhibitors or any of the excipients
  • Depression, generalised anxiety disorder, suicidal ideation
  • Any clinically significant cardiovascular disease (IM, CHF III/IV; AF not controlled by therapy, etc) within 1 year of study entry
  • Any relevant clinically significant cardiovascular condition, clinically abnormal significant 12-lead ECG (QTcF>450 ms for male and >470 for female) or clinically significant laboratory abnormalities
  • Serum potassium value ≤3.5 mEq/L or >5.5mEq/L and/or a fasting serum glucose value ≥140 mg/dL.
  • History or symptoms of significant neurological disease
  • Unstable concurrent disease: eg uncontrolled Thyroid disease or other endocrine diseases, gastrointestinal uncontrolled disease, uncontrolled immune diseases
  • Renal impairment.
  • Patients with abnormal alanine aminotransferase and/ or aspartate aminotransferase and/or bilirubin
  • Current or chronic history of liver disease, or known hepatic or biliary abnormalities and patients receiving treatment with any drug known to have a well defined potential for hepatotoxicity before Study entry
  • Severely obese (BMI ≥35 kg/m2) or have experienced excessive weight loss recently
  • History of alcohol abuse and/or substance/drug abuse within 12 months prior to screening visit.
  • Any recent participation to a clinical Study with other investigational drug

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:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:CHF6001 DOSE1
DOSE1
Dose response: Test one of 4 different doses of CHF6001
其他名称:
  • Dose range finding
实验性的:CHF6001 DOSE2
DOSE2
Dose response: Test one of 4 different doses of CHF6001
其他名称:
  • Dose range finding
实验性的:CHF6001 DOSE3
DOSE3
Dose response: Test one of 4 different doses of CHF6001
其他名称:
  • Dose range finding
实验性的:CHF6001 DOSE4
DOSE4
Dose response: Test one of 4 different doses of CHF6001
其他名称:
  • Dose range finding
安慰剂比较:Matched placebo
placebo control
安慰剂对照
有源比较器:Budesonide
Budesonide DPI 800µg
active control
其他名称:
  • 有源比较器

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
Change from baseline in predose morning FEV1 at 12 weeks
大体时间:week 12
overall effect of CHF6001 on change from baseline in predose morning FEV1
week 12

次要结果测量

结果测量
措施说明
大体时间
Change from baseline in predose morning FEV1 at other timepoints
大体时间:weeks 3, 6, 18, 24
Change from Baseline
weeks 3, 6, 18, 24
Change from baseline in pre-dose morning IC
大体时间:weeks 3, 6, 12, 18, 24
Change from Baseline for other lung function parameters
weeks 3, 6, 12, 18, 24
Change from baseline in pre-dose morning FVC
大体时间:weeks 3, 6, 12, 18, 24
Change from Baseline for other lung function parameters
weeks 3, 6, 12, 18, 24
Change from baseline in TDI focal score
大体时间:weeks 3, 6, 12, 18, 24
Change of TDI score
weeks 3, 6, 12, 18, 24
Change from baseline in SGRQ score
大体时间:weeks 3, 6, 12, 18, 24
Change of SGRQ score
weeks 3, 6, 12, 18, 24
Change from baseline in E-RS score
大体时间:weeks 3, 6, 12, 18, 24
Change of E-RSI score
weeks 3, 6, 12, 18, 24
COPD exacerbation rate over 24 weeks of treatment
大体时间:24 weeks
exacerbation rate
24 weeks
Time to first COPD exacerbation
大体时间:24 weeks
Time to first COPD exacerbation
24 weeks

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。

调查人员

  • 首席研究员:Dave Singh、Medicines Evaluation Unit, Manchester, UK

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)

2016年12月15日

初级完成 (实际的)

2017年10月4日

研究完成 (实际的)

2018年1月9日

研究注册日期

首次提交

2016年11月24日

首先提交符合 QC 标准的

2016年12月5日

首次发布 (估计)

2016年12月8日

研究记录更新

最后更新发布 (实际的)

2019年1月28日

上次提交的符合 QC 标准的更新

2019年1月25日

最后验证

2019年1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

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