DS1040b/Aspirin Drug/Drug Interaction Study
2018年12月20日 更新者:Daiichi Sankyo, Inc.
A PHASE 1, OPEN LABEL, SINGLE DOSE STUDY, TO ASSESS THE SAFETY AND TOLERABILITY OF A SINGLE IV DOSE OF DS-1040B AFTER 5 DAYS OF ASPIRIN TREATMENT IN HEALTHY SUBJECTS
This is a phase 1, open label, single dose study, after 5 days of aspirin treatment, in healthy male and female subjects.
It is hypothesized that co-administering DS-1040b with aspirin at steady state will be safe and well tolerated by healthy male and female subjects.
調査の概要
研究の種類
介入
入学 (実際)
18
段階
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
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London、イギリス、NW10 7EW
- Hammersmith Medicines Research Ltd.
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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
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Healthy male and female subjects, aged 18 to 45 years.
- A body mass index (BMI, or Quetlet index) in the range of 18.0 to 30.0 kg/m2, and weighing between 50 and 100 kg at screening.
- Male subjects have to agree to contraception (condom with spermicide) in addition to having their female partner (if of child-bearing potential) use another form of contraception (e.g., an intrauterine device, diaphragm with spermicide, oral contraceptive, injectable, or sub dermal hormonal implant) from the first dose until 16 weeks following the last dose administration. Also, the male subjects must not donate sperm after the study for a period of four months.
- All women must have a negative serum pregnancy test at screening and a negative urine pregnancy test at admission (Day -1). Women must be of non-childbearing potential either: Surgically sterile (i.e., bilateral tubal ligation or removal of both ovaries and/or uterus at least 6 months prior to dosing) or naturally postmenopausal (spontaneous cessation of menses) for at least 24 consecutive months prior to dosing, with a follicle stimulating hormone (FSH) level at screening of ≥ 40 mIU/mL.
- Sufficient intelligence to understand the nature of the trial and any hazards of participating in it. Ability to communicate satisfactorily with the Investigator and to participate in, and comply with the requirements of, the entire trial.
- Willingness to give written consent to participate after reading the ICF, and after having the opportunity to discuss the trial with the Investigator or his delegate.
- Willingness to give written consent to have data entered into The Overvolunteering Prevention Scheme.
- Willing to abstain from grapefruit/grapefruit juice and Seville oranges from 7 days before the first dose and throughout the study.
- Willing to refrain from consuming food or beverages containing caffeine/xanthine starting 24 hours prior to check-in on Day -1.
Exclusion Criteria:
- Clinically relevant abnormal history, including cardiovascular, haematologic, pulmonary, hepatic, renal, gastrointestinal, connective tissue disease, uncontrolled endocrine/metabolic, oncologic (within the last 5 years), neurologic (including previous transient ischemic attack or stroke), and psychiatric diseases, physical findings, ECG, or laboratory values at the pre-trial screening assessment that could interfere with the objectives of the trial or the safety of the volunteer.
- History of a serious reaction to any medicine.
- History of major bleeding, stomach ulcer, Raynaud's disease, major trauma, or major surgical procedure of any type within 6 months of dosing.
- History of minor bleeding episodes such as epistaxis, rectal bleeding (spots of blood on toilet paper), and gingival bleeding within 3 months before the study treatment.
- Familial or documented or suspected coagulopathy and haemoglobinopathy.
- Females with a history of dysfunctional uterine bleeding, including history of menorrhagia, metrorrhagia, or polymenorrhea.
- History of an operation (e.g. stomach bypass), or a condition that could affect how the body handles or absorbs medicines.
- History of gastro-oesophageal reflux disease.
- Females who are breastfeeding.
- Positive urine or faecal occult blood test at screening or admission (Day -1 or day 1).
- Bleeding time > 9.5 minutes at screening).
- aPTT, PT, INR, or platelet count outside the limit of normal of the clinical laboratory's reference range at screening.
- Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2 (based on Modification of Diet in Renal Disease [MDRD] equation).
- Positive test for hepatitis B, hepatitis C, HIV1 & HIV2.
- QTcF interval duration > 430 msec for males and 450 msec for females, obtained as an average from the 3 ECG measurements on the triplicate screening ECGs.
- Abnormal waveform morphology on any of the ECGs at screening at admission that would preclude accurate measurement of the QT interval duration.
- Physical trauma, dental extraction, surgery, or a significant illness within 4 weeks before the first dose.
- History or presence of keloid, hyperpigmentation, or other adverse reaction to skin injury or surgery.
- Use of any prescribed or non-prescribed (over-the-counter [OTC]) systemic medications (including anticoagulants or antiplatelet medications), topical medications, or herbal supplements within 14 days before the first dose (excluding paracetamol ≤ 2 g/day). St. John's Wort (hypericin) must not have been taken for at least 30 days before the first dose.
- Donated or lost > 400 mL of blood or plasma during 3 months before the first dose on Day 1.
- Donation of blood, plasma, platelets, or any other blood components during the 3 months before the trial, or unwilling to abstain from doing so during the study and for 3 months after receipt of trial medication.
- Participated in a clinical study involving administration of an investigational drug, or a marketed drug within 90 days before administration of the first dose.
- Male subjects who consume more than 21 units of alcohol per week or female subjects who consume more than 14 units of alcohol per week (1 unit of alcohol equals 1/2 pint of beer, a glass of wine, or 1 measure of spirits) or those subjects who have a significant history of alcoholism or drug/chemical abuse within the last 2 years.
- Use of tobacco products or nicotine-containing products within 3 months before the first dose.
- Positive results on tests for drugs of abuse, carbon monoxide, or alcohol at screening or admission.
- Possibility that the volunteer will not cooperate with the requirements of the protocol.
- Objection by General Practitioner (GP) to volunteer entering the trial.
- Known aspirin allergy or intolerance.
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:基礎科学
- 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 |
|---|---|
|
他の:Aspirin
Dispersible tablet, 300mg & 75 mg, once daily for 5 days
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Dispersible tablet, 300mg & 75 mg, once daily for 5 days
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|
実験的:DS-1040b
IV of 6 mg given once over 30 minutes
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IV of 6 mg given once over 30 minutes
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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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
bleeding time
時間枠:day 0 to day 5 after dosing
|
To assess the safety (including bleeding time) and tolerability of a single IV dose of DS-1040b following 5 days aspirin treatment in healthy subjects
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day 0 to day 5 after dosing
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
change in D-dimer level
時間枠:day 0 - day 5 after dosing
|
To assess the effect of a single IV dose of DS-1040b following 5 days aspirin treatment on D-dimer levels
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day 0 - day 5 after dosing
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Cmax
時間枠:Days 5, 6, and 7 after dosing
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Plasma concentration time data of DS-1040a (the free form of DS-1040b) will be analyzed using non-compartmental methods. The following parameters will be estimated and reported: . |
Days 5, 6, and 7 after dosing
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Tmax
時間枠:Days 5, 6, and 7 after dosing
|
Plasma concentration time data of DS-1040a (the free form of DS-1040b) will be analyzed using non-compartmental methods.
The following parameters will be estimated and reported:
|
Days 5, 6, and 7 after dosing
|
|
AUC
時間枠:Days 5, 6, and 7 after dosing
|
Plasma concentration time data of DS-1040a (the free form of DS-1040b) will be analyzed using non-compartmental methods.
The following parameters will be estimated and reported:
|
Days 5, 6, and 7 after dosing
|
|
half-life
時間枠:Days 5, 6, and 7 after dosing
|
Plasma concentration time data of DS-1040a (the free form of DS-1040b) will be analyzed using non-compartmental methods.
The following parameters will be estimated and reported:
|
Days 5, 6, and 7 after dosing
|
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。
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1月1日
一次修了 (実際)
2014年2月1日
研究の完了 (実際)
2014年2月1日
試験登録日
最初に提出
2014年2月21日
QC基準を満たした最初の提出物
2014年2月24日
最初の投稿 (見積もり)
2014年2月25日
学習記録の更新
投稿された最後の更新 (実際)
2018年12月24日
QC基準を満たした最後の更新が送信されました
2018年12月20日
最終確認日
2014年2月1日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- DS1040-A-E102
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
はい
IPD プランの説明
De-identified individual participant data (IPD) and applicable supporting clinical trial documents may be available upon request at https://vivli.org/.
In cases where clinical trial data and supporting documents are provided pursuant to our company policies and procedures, Daiichi Sankyo will continue to protect the privacy of our clinical trial participants.
Details on data sharing criteria and the procedure for requesting access can be found at this web address: https://vivli.org/ourmember/daiichi-sankyo/
IPD 共有時間枠
Studies for which the medicine and indication have received European Union (EU) and United States (US), and/or Japan (JP) marketing approval on or after 01 January 2014 or by the US or EU or JP Health Authorities when regulatory submissions in all regions are not planned and after the primary study results have been accepted for publication.
IPD 共有アクセス基準
Formal request from qualified scientific and medical researchers on IPD and clinical study documents from clinical trials supporting products submitted and licensed in the United States, the European Union and/or Japan from 01 January 2014 and beyond for the purpose of conducting legitimate research.
This must be consistent with the principle of safeguarding study participants' privacy and consistent with provision of informed consent.
IPD 共有サポート情報タイプ
- 研究プロトコル
- 統計分析計画 (SAP)
- インフォームド コンセント フォーム (ICF)
- 臨床試験報告書(CSR)
- 分析コード
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。