Effects of Tipranavir (TPV) and Ritonavir (RTV) on the Pharmacokinetic Characteristics of Tenofovir Disoproxil Fumarate in Healthy Volunteers
2014年9月25日 更新者:Boehringer Ingelheim
A Single Centre, Open-Label, Randomised, Parallel, Multiple Dose Comparison of the Effects of Tipranavir 500 mg and Ritonavir 100 mg or Tipranavir 750 mg and Ritonavir 200 mg Twice a Day for 11.5 Days on the Pharmacokinetic Characteristics of Tenofovir Disoproxil Fumarate 300 mg in Healthy Volunteers
Study to characterise the effects of two dose combinations of tipranavir/ritonavir (TPV 500 mg/RTV 100 mg and TPV 750 mg/RTV 200 mg) administered BID, on the pharmacokinetics of tenofovir disoproxil fumarate as well as the effects of tenofovir disoproxil fumarate on the pharmacokinetics of tipranavir/ritonavir.
調査の概要
研究の種類
介入
入学 (実際)
49
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:
- Ability and willingness to give written informed consent in accordance with institutional and regulatory guidelines and to comply with the investigational nature of the study and the related requirements
- Healthy males or females between 18 and 60 years of age inclusive
- A Body Mass Index >18.5 and <30 kg/m2
- Ability to swallow numerous large capsules without difficulty
- Reasonable probability for completion of the study, in the opinion of the investigator
- Acceptable laboratory values that indicate adequate baseline organ function are required at the time of screening. Laboratory values are considered to be acceptable if severity <= Grade1 based on the AIDS Clinical Trials Group (ACTG) Division of AIDS (DAIDS) Grading Scale. All abnormal laboratory values > Grade 1 (e.g., creatine phosphokinase (CPK), amylase, triglycerides) are subject to approval by the BIPI clinical monitor. Cholesterol <= 240mg/dL at the time of screening is necessary for study entry
- Acceptable medical history, physical examination and ECG are required prior to entering the study
- Willingness to abstain from alcohol for 48 hours prior to Study Day 0 and abstain from alcohol for the duration of the study. In addition, Cabernet Sauvignon must not have been ingested within 15 days prior to Day 0 (Visit 2)
- Willingness to abstain from ingesting grapefruit and grapefruit juice within 15 days of Day 0, Visit 2 and for the duration of the study
- Willingness 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) within 72 hours of pharmacokinetic (PK) sampling days
- Willingness 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:
Female subjects who are of reproductive potential who:
- Have a positive serum B-HCG at Visit 1 or 2 or
- Have not been using regular oral contraception (combined oestrogen and progestogen pill or progestogen only pill) for 3 months and a barrier contraceptive method for at least 30 days prior to Visit 3 (Day 1) or a barrier contraceptive method for at least 3 months prior to Visit 3 (Day 1) or
- Are 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 trial and 30 days after completion/termination or
- Are breast-feeding
- Participation in another trial with an investigational medicine for 30 days prior to Day 0 (Visit 2)
- Ingestion of any known enzyme altering drug (such as phenothiazines, cimetidine, barbiturates, ketoconazole, fluconazole, rifampin, steroids, and herbal medications) for 30 days prior to Day 0 (Visit 2). Use of any other herbal/complementary treatment must be discussed in advance with the monitor and permission obtained prior to study entry
- Ingestion of grapefruit, grapefruit juice, and Cabernet Sauvignon within 15 days prior to Day 0 (Visit 2)
- 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 PK sampling days
- Ingestion of antibiotics within 10 days prior to Day 0 (Visit 2)
- Inability to comply with investigator's instructions
- History of gastrointestinal, hepatic, or renal disorders within 60 days
- History of alcohol abuse
- Current use of cigarettes defined as greater than 10 cigarettes per day or rolling/pipe tobacco equivalent
- Blood or plasma donations within 30 days prior to Day 0 (Visit 2)
- 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 confound the results of the study or pose additional risk in administering tipranavir or ritonavir or tenofovir disoproxil fumarate to the subject
- Subjects who have had an acute illness within 2 weeks prior to Day 0 (Visit 2)
- Subjects who are currently taking any over-the-counter drug within 7 days prior to Day 0, (Visit 2) or who are currently taking any prescription drug that, in the opinion of the investigator in consultation with the clinical monitor and pharmacokineticist, might interfere with either the absorption, distribution or metabolism of the test substances
- Hypersensitivity to tipranavir, ritonavir, or tenofovir disoproxil fumarate
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:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:tipranavir/ritonavir low dose
|
|
|
実験的:tipranavir/ritonavir high dose
|
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 plasma concentration time curve from 0-24 hours (AUC0-24) for tenofovir
時間枠:up to 24 hours
|
up to 24 hours
|
|
Area under plasma concentration time curve from 0-12hours (AUC0-12) for tipranavir/ritonavir
時間枠:up to 12 hours
|
up to 12 hours
|
|
Maximum plasma concentration (Cmax)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Drug concentration in plasma at 12 hours after administration (C12h) for tenofovir
時間枠:up to 12 hours
|
up to 12 hours
|
|
Drug concentration in plasma at 12 hours after administration (C12h) for tipranavir/ritonavir
時間枠:up to 12 hours
|
up to 12 hours
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
定常状態での最大血漿濃度 (Cmax,ss)
時間枠:24時間まで
|
24時間まで
|
|
Trough plasma concentration at steady state (Cmin)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Mean residency time (MRT)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Apparent terminal half life (T1/2)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Time of maximum concentration (Tmax)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Oral clearance (CL/F)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Apparent volume of distribution during the terminal elimination phase, divided by F (bioavailability factor) (Vz/F)
時間枠:up to 24 hours
|
up to 24 hours
|
|
Number of subjects with clinically significant findings in vital signs (pulse rate, blood pressure)
時間枠:up to 14 days
|
up to 14 days
|
|
Number of subjects with clinically significant findings in physical examination
時間枠:up to 14 days
|
up to 14 days
|
|
Number of subjects with clinically significant findings in electrocardiogram
時間枠:up to 14 days
|
up to 14 days
|
|
Number of subjects with clinically significant findings in laboratory tests
時間枠:up to 14 days
|
up to 14 days
|
|
Number of subjects with adverse events
時間枠:up to 14 days
|
up to 14 days
|
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
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
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
2002年5月1日
一次修了 (実際)
2002年6月1日
試験登録日
最初に提出
2014年9月25日
QC基準を満たした最初の提出物
2014年9月25日
最初の投稿 (見積もり)
2014年9月29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29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25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
- 1182.46
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