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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of BI 1744 CL in Healthy Male and Female Volunteers

2014年6月20日 更新者:Boehringer Ingelheim

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2.5 μg, 10 μg, and 30 μg) of BI 1744 CL for 14 Days in Healthy Male and Female Volunteers (Doubleblind, Randomised, Placebo Controlled [at Each Dose Level] Study)

To investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1744 CL

調査の概要

状態

完了

条件

研究の種類

介入

入学 (実際)

47

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~50年 (大人)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Healthy male or female based upon a complete medical history, including the physical examination, regarding vital signs (blood pressure (BP), pulse rate (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 ≤50 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 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 randomisation
  • 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 60 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).

For female subjects:

  • Pregnancy
  • Positive pregnancy test
  • No adequate contraception e.g. oral contraception, sterilisation, IUD (intrauterine device). Females who are not surgically sterile will be asked to additionally use barrier contraception methods (e.g. condoms) prior to administration of study medication, during the study and at least 2 months after release from the study.
  • Inability to maintain this adequate contraception during the whole study period
  • Lactation period

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 multiple rising doses
実験的:BI 1744 CL medium dose, females

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
時間枠
Number of patients with clinically significant changes in physical examination
時間枠:Baseline, day 32 (end-of-study examination)
Baseline, day 32 (end-of-study examination)
Number of patients with clinically significant changes in vital signs
時間枠:Baseline, up to day 32
Baseline, up to day 32
Number of patients with clinically significant changes in 12-lead ECG (Electrocardiogram)
時間枠:Baseline, up to day 32
Baseline, up to day 32
Number of patients with abnormal changes in laboratory tests
時間枠:Baseline, up to day 32
Baseline, up to day 32
Changes in airway resistance (Raw) measured by body plethysmography
時間枠:Baseline, up to day 32
Baseline, up to day 32
Changes in tremormetry parameters
時間枠:Baseline, up to day 32
Baseline, up to day 32
Number of patients with adverse events
時間枠:Up to day 32
Up to day 32
Assessment of tolerability by the investigator on a 4-point scale
時間枠:Day 32 (end-of-study examination)
Day 32 (end-of-study examination)

二次結果の測定

結果測定
時間枠
Cmax (maximum concentration of the analyte in plasma)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
tmax (time from dosing to maximum concentration)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
AUC (area under the concentration-time curve of the analyte in plasma at different time points)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
Aet1-t2(amount of analyte that is eliminated in urine from the time point t1 to time point t2)
時間枠:Up to 384 hours after drug administration
Up to 384 hours after drug administration
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)
時間枠:Up to 384 hours after drug administration
Up to 384 hours after drug administration
%AUCtz-∞ (the percentage of the AUC 0-∞ that is obtained by extrapolation)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
λz (terminal rate constant of the analyte in plasma)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
t½ (terminal half-life of the analyte in plasma)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
MRTih (mean residence time of the analyte in the body after inhalation)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
CL/F (apparent clearance of the analyte in the plasma after extravascular administration)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
Vz/F (apparent volume of distribution of the analyte during the terminal phase λz following an extravascular dose)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
CLR,t1-t2 (renal clearance of the analyte in plasma from the time point t1 until the time point t2)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
RA,Cmax,14 based on Cmax (Accumulation ratio of the analyte in plasma after multiple dose administration over a uniform dosing interval τ)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
RA,AUC,14 based on AUC0-τ
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
Cmin,ss (minimum measured concentration of the analyte in plasma at steady state over a uniform dosing interval τ)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
Cpre,ss (predose concentration of the analyte in plasma at steady state immediately before administration of the next dose)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration
Linearity Index (LI)
時間枠:Up to 408 hours after drug administration
Up to 408 hours after drug administration

協力者と研究者

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出版物と役立つリンク

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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

2006年1月1日

一次修了 (実際)

2006年9月1日

試験登録日

最初に提出

2014年6月20日

QC基準を満たした最初の提出物

2014年6月20日

最初の投稿 (見積もり)

2014年6月24日

学習記録の更新

投稿された最後の更新 (見積もり)

2014年6月24日

QC基準を満たした最後の更新が送信されました

2014年6月20日

最終確認日

2014年6月1日

詳しくは

本研究に関する用語

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