Study of Tipranavir and Ritonavir on the Pharmacokinetic Characteristics of Methadone Administered in Healthy Volunteers
2014年9月18日 更新者:Boehringer Ingelheim
A Single-centre, Open-label Study of Multiple Doses of Tipranavir 500 mg and Ritonavir 200 mg (Twice Daily) on the Pharmacokinetic Characteristics of Methadone Administered as a Single Dose in Healthy Volunteers
The primary objective of this study is to characterise the effects of tipranavir 500 mg and ritonavir 200 mg (TPV/r; given twice daily) at steady-state on the pharmacokinetics of methadone administered as a single dose in healthy adult volunteers
調査の概要
研究の種類
介入
入学 (実際)
15
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
18年~60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
全て
説明
Inclusion Criteria:
- Male or female healthy volunteers aged at least 18 to 60 years.
- Clinically normal medical history.
- Clinically normal findings on physical examination.
- Clinically normal laboratory values.
- A Body Mass Index >18.5 and <30 kg/m2.
- Able to swallow large capsules without difficulty.
- Capable of comprehending and communicating effectively with the investigator and staff and of providing written informed consent in accordance with ethics committee and regulatory guidelines.
- Willing to stay in the study centre for the duration of the study.
- Willing to abstain from ingesting substances during the study which may alter plasma study drug levels by interaction with the cytochrome P450 system.
- Willing to abstain from alcohol for 48 hours prior to Visit 1 and for the duration of the study. In addition, Cabernet Sauvignon must not have been ingested within 15 days prior to Visit 1.
- Willing to abstain from ingesting grapefruit and grapefruit juice for 15 days before Visit 1 and for the duration of the study.
- Willing to abstain from ingesting Seville oranges, strawberries or strawberry extract, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) for 72 hours before the pharmacokinetic sampling days.
- Willing to abstain from use of tobacco products for the duration of the study.
- Urine drug screen negative for illegal non-prescription drugs.
- Negative HIV serology.
- Negative for Hepatitis B surface antigen and Hepatitis C
Exclusion Criteria:
- Any clinically significant disease. (A significant disease was defined as a disease which in the opinion of the investigator may either have put the subject at risk because of participation in the study or a disease which may have influenced the results of the study or the subject's ability to participate in the study.)
- Clinically significant abnormal baseline haematology, blood chemistry or urinalysis findings.
- Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), cholesterol, triglyceride or glucose greater than the upper limit of normal at Visit 1.
- Treatment with prohibited medications in the thirty days before the study or during the study or ingestion of drugs of abuse.
- Treatment with any investigational drug within 90 days of the first dose of study medication.
- Inability to adhere to the requirements of the protocol (including active substance abuse) as assessed by the investigator.
- Prior tipranavir use.
- Ingestion of any known enzyme altering drug (such as phenothiazines, cimetidine, barbiturates, ketoconazole, fluconazole, clarithromycin, rifampin, steroids, and herbal medications) for thirty days prior to Visit 1.
- Ingestion of grapefruit, grapefruit juice, and Cabernet Sauvignon within fifteen days prior to Visit 1.
- Ingestion of Seville oranges, strawberries or strawberry extract, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) within 72 hours of pharmacokinetics sampling days.
- Treatment with prescription medicines within thirty days prior to Visit 1.
- History of gastrointestinal, hepatic, or renal disorders within 60 days prior to Visit 1.
- Any history of alcohol or drug abuse.
- Current use of cigarettes defined as greater than 10 cigarettes per day or rolling/pipe tobacco equivalent.
- Blood or plasma donations within 90 days prior to Visit 1
- Subjects with a seated systolic blood pressure either <100 mm Hg or >150 mm Hg; resting heart rate either <50 beats/min or >100 beats/min.
- Subjects with a history of any illness or allergy that, in the opinion of the investigator, might have confounded the results of the study or posed additional risk in administering tipranavir, ritonavir or methadone to the subject.
- Subjects who had an acute illness within two weeks prior to Visit 1.
- Subjects who were currently taking any over-the-counter drug within fourteen days prior to Visit 1 or who were currently taking any prescription drug.
- Hypersensitivity to tipranavir, ritonavir, or methadone.
- Female subjects who are of reproductive potential and who were pregnant, breastfeeding, had a positive serum B-HCG at Visit 1 or 2, had not been using a barrier contraceptive method for at least three months prior to Study Day 1 or were not willing to use a reliable method of double-barrier contraception (such as diaphragm with spermicidal cream/jelly or condoms with spermicidal foam) during the study and for thirty days after completion or termination of the study.
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:非ランダム化
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
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 |
|---|---|
|
Area under the concentration-time curve for 0 to 24 hours (AUC0-24h) of methadone
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
Maximum concentration (Cmax)
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
Concentration at 6 hours (C6h) of methadone
時間枠:6 hours after drug administration
|
6 hours after drug administration
|
|
Area under the concentration-time curve for 0 to 12 hours (AUC0-12h) of tipranavir and ritonavir
時間枠:up to 12 hours after drug administration
|
up to 12 hours after drug administration
|
|
concentration at 12 hours (C12h) of tipranavir and ritonavir
時間枠:12 hours after drug administration
|
12 hours after drug administration
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
mean residence time (MRT)
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
apparent terminal half-life (t½)
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
time to maximum concentration (Tmax)
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
oral clearance (CL/F)
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
apparent volume of distribution during the terminal elimination phase divided by the bioavailability factor (Vz/F)
時間枠:up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
Number of patients with abnormal findings in physical examination
時間枠:Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
|
Number of patients with clinically significant changes in vital signs
時間枠:Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
|
Number of patients with abnormal changes in clinical laboratory parameters
時間枠:Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
|
Number of participants with adverse events
時間枠:Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
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。
スポンサー
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
2005年1月1日
一次修了 (実際)
2005年2月1日
試験登録日
最初に提出
2014年9月18日
QC基準を満たした最初の提出物
2014年9月18日
最初の投稿 (見積もり)
2014年9月19日
学習記録の更新
投稿された最後の更新 (見積もり)
2014年9月19日
QC基準を満たした最後の更新が送信されました
2014年9月18日
最終確認日
2014年9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
- 1182.26
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