Pharmacokinetic Study in Elderly Patients With Chronic Obstructive Bronchitis (COPD)
2014年6月20日 更新者:Boehringer Ingelheim
The Pharmacokinetics, Safety and Tolerability of Tiotropium in Elderly COPD Patients (Open Label, Monocenter Study).
Study to evaluate the pharmacokinetics of tiotropium following 14 days of administration (18µg once per day) in elderly COPD patients.
研究概览
研究类型
介入性
注册
29
阶段
- 第三阶段
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
- 孩子
- 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:
All patients were required to have a diagnosis of COPD and to meet the following spirometric criteria:
- Relatively stable, moderate to severe airway obstruction with an FEV1 ≤ 65% of predicted normal and FEV1/FVC ≤ 70%
Patients were required to have normal renal clearance. Renal clearance will be evaluated by the determination of creatinine clearance. To qualify for this trial, the patient's measured creatinine clearance was required to be within 20% of the calculated creatinine clearance, as given by the following equations:
- Males: Calculated Creatinine Clearance (ml/min) = [140 - Age (yrs)] x weight(kg) / 72 x serum creatinine (mg/dL)
- Females: Calculated Creatinine Clearance (ml/min) = [140 - Age (yrs)] x weight (kg) / 85 x serum creatinine (mg/dL)
- Both male or female patients were eligible. Twelve patients ≥ 70 years old and twelve patients ≤ 50 years
- Patients were required to have a smoking history of more than ten pack-years, where a pack-year was defined as the equivalent of smoking one pack of cigarettes per day for a year
- Patients must be able to perform all specified procedures and maintain records during the study period as required in the protocol
- Patients were required to be able to inhale medication from the HandiHaler®
- Patients were required to sign an Informed Consent Form prior to participation in the trial, including any necessary prior to pre-study washout of their usual pulmonary medications
Exclusion Criteria:
- Patients with significant diseases other than COPD were excluded from participation in the trial. A significant disease was defined as a disease which in the opinion of the investigator may either have put the patient at risk because of participation in the trial or a disease which may have influenced the results of the trial or the patient's ability to participate in the trial;
- Patients with clinically significant abnormal baseline haematology, blood chemistry or urinalysis, if the abnormality defined a disease listed as an exclusion criterion;
- Patients with alanine transaminase (ALT/SGOT) > 80 IU/L or aspartate transaminase (AST/SGPT) > 80 IU/L, or bilirubin > 2.0 mg/dL or creatinine > 2.0 mg/dL were excluded from participation in the trial, regardless of the patient's clinical condition. Repeat laboratory evaluations were not conducted in these patients;
- Patients with a recent history (i.e., one year or less) of myocardial infarction (MI);
- Patients with a recent history (i.e., three years or less) of heart failure or patients with any cardiac arrhythmia requiring drug therapy;
- Patients with regular use of daytime oxygen therapy;
- Patients with known active tuberculosis;
- Patients with a history of cancer within the last five years. However, patients with treated basal cell carcinoma are allowed to participate;
- Patients with a history of life-threatening pulmonary obstruction, or a history of cystic fibrosis or bronchiectasis;
- Patients who had undergone thoracotomy with pulmonary resection. Patients with a history of a thoracotomy for other reasons were evaluated as per exclusion criterion # 1;
- Patients who had developed an upper respiratory tract infection in six weeks prior to the Screening Visit (Visit 1) or during the baseline period;
- Patients with known hypersensitivity to anticholinergic drugs, lactose or any other components of the inhalation capsule delivery system;
- Patients with known symptomatic prostatic hypertrophy or bladder neck obstruction;
- Patients with known narrow-angle glaucoma;
- Patients treated with cromolyn sodium or nedocromil sodium;
- Patients treated with antihistamines (H1 receptor antagonists);
- Patients using oral corticosteroid medication at unstable doses (i.e. less than six weeks on a stable dose) or at a dose in excess of the equivalent of 10 mg of prednisone per day (or 20 mg every other day);
- Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception (i.e. oral contraceptives, intrauterine devices, diaphragm or Norplant®);
- Patients with a history of asthma, allergic rhinitis or atopy or patients with a total blood eosinophil count ≥ 600/mm3. A repeat eosinophil count was not conducted in these patients;
- Patients with history and/or active alcohol or drug abuse.
- Patients who had taken an investigational drug within one month or six half lives (whichever was greater) prior to Screening Visit (Visit 1).
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:噻托溴铵吸入胶囊
|
Powder inhalation via HandiHaler®
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Total area under the plasma drug concentration-time curve (AUC 0-4 h)
大体时间:pre-dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre-dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
|
Urinary excretion of tiotropium (Ae(0-4 hours))
大体时间:screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
|
Renal clearance of tiotropium (CLren)
大体时间:screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
|
Terminal elimination half-life after the last dose
大体时间:pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Plasma concentration of drug 5 min after inhalation (C5min)
大体时间:pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
|
tmax (time of occurrence for maximum drug concentration)
大体时间:pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
|
Change from baseline in FEV1 (Forced expiratory volume in one second)
大体时间:Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
Change from baseline in FVC (Forced vital capacity)
大体时间:Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
FEV1/FVC
大体时间:Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
Symptom evaluation
大体时间:2 weeks
|
2 weeks
|
|
Use of salbutamol
大体时间:2 weeks
|
2 weeks
|
|
Occurrence of Adverse Events
大体时间:up to day 39
|
up to day 39
|
|
Occurrence of Adverse Events
大体时间:up to day 38
|
up to day 38
|
|
Changes form baseline in vital signs (pulse rate and blood pressure)
大体时间:up to day 38
|
up to day 38
|
|
Changes from baseline in laboratory tests (haematology, clinical chemistry and urinalysis)
大体时间:baseline, day 38
|
baseline, day 38
|
|
Changes from baseline in physical examination
大体时间:baseline, day 38
|
baseline, day 38
|
|
Changes from baseline in ECG (Electrocardiogram)
大体时间:baseline, day 1, 7, 14 and 38
|
baseline, day 1, 7, 14 and 38
|
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
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有用的网址
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
1998年2月1日
初级完成 (实际的)
1998年9月1日
研究注册日期
首次提交
2014年6月20日
首先提交符合 QC 标准的
2014年6月20日
首次发布 (估计)
2014年6月24日
研究记录更新
最后更新发布 (估计)
2014年6月24日
上次提交的符合 QC 标准的更新
2014年6月20日
最后验证
2014年6月1日
更多信息
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