Effect of Opicapone at Steady State on Warfarin Pharmacokinetics
2014年11月28日 更新者:Bial - Portela C S.A.
Effect of Opicapone at Steady State on Warfarin Pharmacokinetics in Healthy Volunteers
Single-centre, open-label, fixed-sequence design consisting of 2 periods separated by a washout period of at least 14 days.
調査の概要
詳細な説明
Single-centre, open-label, fixed-sequence design consisting of 2 periods separated by a washout period of at least 14 days.
In Period 1, a single dose of 25 mg warfarin was administered alone.
In Period 2, subjects received 475 mg OPC, on Day 1 and D2 followed by 50 mg OPC once daily for 5 days (D3 to D7).
On D8, 50 mg OPC was administered with a single dose of 25 mg warfarin.
研究の種類
介入
入学 (実際)
20
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~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
全て
説明
Inclusion Criteria:
- A signed and dated informed consent form before any study-specific screening procedure was performed,
- Male or female subjects aged 18 to 45 years, inclusive,
- Body mass index (BMI) between 18 and 30 kg/m2,
- Healthy as determined by pre-study medical history, physical examination, vital signs, complete neurological examination and 12-lead electrocardiogram (ECG),
- Negative tests for hepatitis B surface antigen (HBsAg), anti-hepatitis C virus (HCV) antibodies and anti-human immunodeficiency virus (HIV) antibodies at screening,
- Clinical laboratory test results clinically acceptable at screening and at admission to each inpatient period,
- Negative screen for alcohol and drugs of abuse at screening and at admission to each inpatient period,
- Non-smokers or ex-smokers for at least 3 months,
- Able to participate, and willing to give written informed consent and comply with the study restrictions,
- Able to swallow a high number of capsules within a short time frame,
If female:
- Was not of childbearing potential by reason of surgery or, if of childbearing potential, used an effective non-hormonal method of contraception (intrauterine device or intrauterine system; condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; true abstinence; or vasectomized male partner, provided that he was the sole partner of that subject) for the entire duration of the study,
- Negative serum pregnancy test at screening and a negative urine pregnancy test at admission to each inpatient period.
Exclusion Criteria:
- Any clinically relevant history or presence of respiratory, gastrointestinal, renal, hepatic, haematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, endocrine, connective tissue diseases or disorders, or had a clinically relevant surgical history,
- Any personal or family history of haemostatic disorder,
- Any personal or family history of bleeding complications after surgery or tooth extraction, nose or gingival bleeding, or haemorrhagic diathesis,
- Any clinically relevant findings in the laboratory tests, particularly any abnormality in the coagulation tests or the liver function tests,
- History of relevant atopy or drug hypersensitivity,
- History of alcoholism and/or drug abuse,
- Current consumption of more than 14 units of alcohol per week [1 unit of alcohol = 280 mL beer (3-4°) = 100 mL wine (10-12°) = 30 mL spirits (40°)],
- Any significant infection or known inflammatory process on screening or admission to each treatment period; any acute gastrointestinal symptoms (e.g., nausea, vomiting, diarrhoea, heartburn) at the time of screening or admission to each treatment period,
- Use of medicines within 2 weeks of admission to first period that could affect the subject's safety or other study assessments, in the investigator's opinion, or intake of any of the prohibited medications (i.e., CYP2C9 inhibitor taken within 1 week prior to start of administration of study drug, and CYP2C9 inducer taken within 4 weeks prior to dosing),
- Previous use of opicapone,
- Use of any investigational drug or participation in any clinical trial within 3 months prior to screening; participation in more than 2 clinical trials within the 12 months prior to screening,
- Blood donation or receipt of any blood transfusion or any blood products within the 3 months prior to screening,
- Vegetarian, vegan or had medical dietary restrictions,
- Not able to communicate reliably with the investigator,
- Unlikely to co-operate with the requirements of the study,
- Unwilling or unable to give written informed consent,
- CYP2C9 poor metaboliser, as assessed by genotyping,
If female:
- Pregnant or breast-feeding.
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)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:BIA 9-1067 / Warfarin
BIA 9-1067 capsules of 25 mg or 50 mg Warfarin capsules of 5 mg
|
他の名前:
他の名前:
|
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 |
|---|---|
|
R- and S-warfarin plasma concentration
時間枠:pre-dose and 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48, 60, 72, 96, 120 and 144 h post-warfarin
|
pre-dose and 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48, 60, 72, 96, 120 and 144 h post-warfarin
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Opicapone plasma concentration
時間枠:D1 pre-dose, and on D8 at the following time points: pre-dose, 0.5, 2, 4, 6, and 8 h post-opicapone dose
|
D1 pre-dose, and on D8 at the following time points: pre-dose, 0.5, 2, 4, 6, and 8 h post-opicapone dose
|
|
BIA 9-1103 (sulphate metabolite) plasma concentration
時間枠:D1 pre-dose and from D5 to D7 pre-dose, and on D8 at the following time points: pre-dose, 0.5, 2, 4, 6, 8, 24, 48, 72 and 144 h post-opicapone dose.
|
D1 pre-dose and from D5 to D7 pre-dose, and on D8 at the following time points: pre-dose, 0.5, 2, 4, 6, 8, 24, 48, 72 and 144 h post-opicapone dose.
|
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
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
2014年3月1日
一次修了 (実際)
2014年5月1日
研究の完了 (実際)
2014年5月1日
試験登録日
最初に提出
2014年11月28日
QC基準を満たした最初の提出物
2014年11月28日
最初の投稿 (見積もり)
2014年12月2日
学習記録の更新
投稿された最後の更新 (見積もり)
2014年12月2日
QC基準を満たした最後の更新が送信されました
2014年11月28日
最終確認日
2014年11月1日
詳しくは
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