Safety/Tolerability, Pharmacokinetics, and Pharmacodynamics of BIBB 1464 MS in Healthy Male Subjects, Combined With Preliminary Evaluation of Relative Bioavailability and Effect of Food
Safety/Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Oral Doses of 0.25 mg, 0.75 mg, 2 mg, 6 mg, and 10 mg BIBB 1464 MS (Tablet) in Healthy Male Subjects, Combined With Preliminary Evaluation of Relative Bioavailability and Effect of Food of the Dose of 0.75 mg or 2 mg or 6 mg (Two-stage Trial Design With Randomised Double Blind Placebo Controlled Rising Dose Phase and Subsequent Randomised, Open Parallel Group Phase)
Safety, pharmacodynamics and pharmacokinetics of 0.25, 0.75, 2.0, 6.0, and 10 mg BIBB 1464 p.o once daily in a rising dose group-comparison (placebo controlled, double blind, randomized per dose level).
Relative Bioavailability of 0.75 mg or 2 mg or 6 mg ( tablet vs. solution, intraindividual comparison), preliminary assessment of food effects (interindividual comparison)
Two-stage Trial Design With Randomised Double Blind Placebo Controlled Rising Dose Phase and Subsequent Randomised, Open Parallel Group Phase).
MS (Tablet) in Healthy Male Subjects, Combined With Preliminary Evaluation of Relative Bioavailability and Effect of Food of the Dose of 0.75 mg or 2 mg or 6 mg (Two-stage Trial Design With Randomised Double Blind Placebo Controlled Rising Dose Phase and Subsequent Randomised, Open Parallel Group Phase).
調査の概要
状態
条件
研究の種類
入学 (実際)
段階
- フェーズ 1
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Healthy subjects as determined by results of screening
- Signed written informed consent in accordance with good clinical practice (GCP) and local legislation
- Age > 18 and < 55 years
- Broca > - 20% and < + 20%
Exclusion Criteria:
- Any findings of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance.
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal (including thyroid) disorder
- Surgery of the gastro-intestinal tract (except appendectomy)
- Disease of the central nervous system (such as epilepsy) or psychiatric disorders
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
- Intake of drugs with a long half-life (> 24 hours) (<= 1 month prior to administration or during the trial)
- Use of any drugs which might influence the result of the trial (<= 10 days prior to administration or during the trial)
- Participation in another trial with an investigational drug (<= 2 month prior to administration or during the trial)
- Smoker (> 10 cigarettes or > 3 cigars or >3 pipes/day)
- Inability to refrain from smoking during the period of the study
- Known alcohol (>60 g/day) or drug abuse
- Blood donation (<=1 month prior to administration)
- Excessive physical activities (<5 days prior to administration)
- Any laboratory value outside the normal range of clinical relevance
- History of hemorrhagic diatheses
- History of gastro-intestinal ulcer, perforation or bleeding
- History of bronchial asthma
研究計画
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 |
|---|---|
|
実験的:BIBB 1464 MS single rising dose fed
|
|
|
実験的:BIBB 1464 MS tablet fasted
|
|
|
アクティブコンパレータ:BIBB 1464 MS solution fasted
|
|
|
プラセボコンパレーター:BIBB 1464 MS placebo
|
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 |
|---|---|
|
有害事象のある患者数
時間枠:最後の薬剤投与後 72 時間以内
|
最後の薬剤投与後 72 時間以内
|
|
Maximum drug plasma concentration (Cmax)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Time to reach the maximum concentration of the analyte in plasma (tmax)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Total area under the plasma drug concentration-time curve (AUC)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Apparent terminal half-life of the analyte in plasma (t1/2)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Total plasma clearance divided by the systemic availability factor (CL/f)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Dose normalized AUC0-38h ( NAUC0-38h)
時間枠:Up to 38 h after drug administration
|
Up to 38 h after drug administration
|
|
Mean residence time, total (MRTtot)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Number of patients with clinical significant findings in vital signs
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Number of patients with clinical significant findings in electrocardiogram (ECG)
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Number of patients with clinical significant findings in physical examination
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Investigator assessed tolerability on a 4 point scale
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Monoepoxysqualene (MES) plasma concentration
時間枠:Up to 38 hours after drug administration
|
Up to 38 hours after drug administration
|
|
Amount of drug excreted in urine
時間枠:Up to 38 h after drug administration
|
Up to 38 h after drug administration
|
協力者と研究者
スポンサー
出版物と役立つリンク
便利なリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- 1178.1
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。