Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses of BI 1744 CL in Fixed Dose Combination With Tiotropium Bromide in Healthy Male Volunteers
2014年10月7日 更新者:Boehringer Ingelheim
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2 μg/5 μg, 10 μg/5 μg, and 40 μg/10 μg) of BI 1744 CL in Fixed Dose Combination With Tiotropium Bromide for 14 Days in Healthy Male Volunteers (Double-blind, Randomised, Placebo Controlled [at Each Dose Level] Study)
To investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1744 CL and Tiotropium Bromide when given as fixed dose combination
調査の概要
状態
完了
条件
研究の種類
介入
入学 (実際)
36
段階
- フェーズ 1
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
21年~45年 (大人)
健康ボランティアの受け入れ
はい
受講資格のある性別
男
説明
Inclusion Criteria:
- Healthy male based upon a complete medical history, including physical examination, regarding vital signs (BP, PR), 12-lead ECG measurement, and clinical laboratory tests. There is no finding deviating from normal and of clinical relevance. There is no evidence of a clinically relevant concomitant disease
- Age ≥21 and ≤45 years
- BMI ≥18.5 and <30 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with good clinical practice (GCP) and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including BP, PR, and ECG measurements) deviating from normal and of clinical relevance
- Evidence of a clinically relevant concomitant disease
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of relevant orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections
- History of relevant allergy/hypersensitivity (including allergy to the drug or its excipients) as judged clinically relevant by the investigator
- Intake of drugs with a long half-life (>24 hours) within at least 1 month or less than 10 half-lives of the respective drug prior to randomization
- Use of drugs which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 10 days prior to randomisation
- Participation in another trial with an investigational drug within 2 months prior to randomisation
- Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
- Inability to refrain from smoking on trial days as judged by the investigator
- Alcohol abuse (more than 40 g alcohol a day)
- Drug abuse
- Blood donation (more than 100 mL blood within 4 weeks prior to randomisation or during the trial)
- Excessive physical activities within 1 week prior to randomisation or during the trial
- Any laboratory value outside the reference range that is of clinical relevance
- Inability to comply with dietary regimen of the study centre
The following exclusion criteria are specific for this study due to the known class side effect profile of ß2-mimetics:
- Asthma or history of pulmonary hyperreactivity
- Hyperthyrosis
- Allergic rhinitis in need of treatment
- Clinically relevant cardiac arrhythmia
- Paroxysmal tachycardia (>100 beats per minute)
The following exclusion criteria are specific for this study due to the known class side effect profile of Tiotropium:
- Hypersensitivity to tiotropium and/or related drugs of these classes
- History of narrow-angle glaucoma
- History of prostatic hyperplasia
- History of bladder-neck obstruction
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
プラセボコンパレーター:プラセボ
|
|
|
実験的:BI 1744 CL in combination with Tiotropium
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of subjects with clinically relevant findings in physical examination
時間枠:Up to day 32
|
Up to day 32
|
|
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Number of subjects with clinically relevant findings in vital signs
時間枠:Up to day 32
|
blood pressure, pulse rate
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Up to day 32
|
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Number of subjects with clinically relevant findings in 12-lead ECG
時間枠:Up to day 32
|
Up to day 32
|
|
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Number of subjects with clinically relevant findings in laboratory tests
時間枠:Up to day 32
|
Up to day 32
|
|
|
Number of subjects witch clinically relevant changes in additional safety laboratory test parameters
時間枠:up to 318 hours after start of treatment
|
Systemic metabolic parameters: cyclic adenosine mono phosphate (cAMP) and potassium
|
up to 318 hours after start of treatment
|
|
Number of subjects with clinically relevant changes in airway resistance (Raw) measured by body plethysmography
時間枠:Pre-dose, up to 408 hours after start of treatment
|
Pre-dose, up to 408 hours after start of treatment
|
|
|
Number of subjects with adverse events
時間枠:Up to day 32
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Up to day 32
|
|
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Global assessment of tolerability by investigator on a 4-point scale
時間枠:Up to day 32
|
Up to day 32
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Maximum concentration in plasma (Cmax)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Time from dosing to maximum concentration in plasma (tmax)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Area under the concentration-time curve in plasma (AUC)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Area under the concentration-time curve in plasma over the time interval from 0 extrapolated to infinity (AUC0-∞)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Percentage of AUC 0-∞ that is obtained by extrapolation (%AUCtz-∞)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Terminal rate constant in plasma (λz)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Terminal half-life in plasma (t½)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Mean residence time in the body after inhalation (MRTih)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Apparent clearance after extravascular administration (CL/F)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
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Apparent volume of distribution during the terminal phase λz following an extravascular dose (Vz/F)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Amount eliminated in urine from the time point t1 to t2 (Aet1-t2)
時間枠:up to 336 hours after start of treatment
|
up to 336 hours after start of treatment
|
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Fraction excreted in urine from time point t1 to t2 (fet1-t2)
時間枠:up to 336 hours after start of treatment
|
up to 336 hours after start of treatment
|
|
Renal clearance from the time point t1 until the time point t2 (CLR,t1-t2)
時間枠:up to 504 hours after start of treatment
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up to 504 hours after start of treatment
|
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Minimum measured concentration in plasma at steady state over a uniform dosing interval τ (Cmin,ss)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Predose concentration of the analytes in plasma at steady state immediately before administration of the next dose (Cpre,ss)
時間枠:Pre-dose every 24 hours
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Pre-dose every 24 hours
|
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Time of last measurable concentration in plasma (tz)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Linearity index (LI)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
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Accumulation ratio based on Cmax (RA,Cmax)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Accumulation ratio based on AUCτ (RA,AUC)
時間枠:up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
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便利なリンク
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始
2007年4月1日
一次修了 (実際)
2007年9月1日
試験登録日
最初に提出
2014年10月7日
QC基準を満たした最初の提出物
2014年10月7日
最初の投稿 (見積もり)
2014年10月9日
学習記録の更新
投稿された最後の更新 (見積もり)
2014年10月9日
QC基準を満たした最後の更新が送信されました
2014年10月7日
最終確認日
2014年10月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 1237.2
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