이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

Multiple Dose Study of D1971a in Healthy Volunteers

2017년 4월 27일 업데이트: Daiichi Sankyo, Inc.

A Phase I, Double-Blind, Randomised, Placebo Controlled, Multiple-Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DS-1971a in Healthy Male and Female Subjects

This is a randomised, double-blind, placebo-controlled multiple dose study designed to explore the safety, tolerability and PK of DS-1971a following oral administration over 14 days to healthy male and female subjects. Each participant receives lidocaine as a local anaesthetic before inserting the intravenous cannula.

연구 개요

상태

완전한

정황

상세 설명

Within strictly defined limits, the protocol permits the dose escalation committee to amend the dose escalation rules, doses proposed in the study protocol and to change the timing of or to add additional assessments following review of the safety, tolerability and plasma DS-1971a concentration data. The decisions to change the doses will be documented in the minutes of the dose escalation committee.

연구 유형

중재적

등록 (실제)

25

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • London, 영국
        • Mammersmith Medicines Research Ltd.

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Healthy male and female subjects aged 18 years to 65 years.
  • A body mass index (BMI) in the range 18 kg/m2 to 30 kg/m2, inclusive, and weighing between 50 kg and 100 kg, inclusive at screening. BMI is calculated as weight [kg]/(height [m])2.
  • Female subjects must be of non-childbearing potential as follows:

    • Must be postmenopausal (the last menstrual period was at least 12 months before Screening, and a follicle stimulating hormone [FSH] test at Screening confirms postmenopausal status); or
    • Must be surgically sterile having undergone hysterectomy, bilateral oophorectomy, bilateral salpingectomy and/or bilateral tubal ligation.
  • Willing to comply with all study restrictions, including the use of contraception, concomitant medication, and dietary and lifestyle restrictions.
  • Sufficient intelligence to understand the nature of the study and any hazards of participating in it. Ability to communicate satisfactorily with the Investigator and to participate in, and comply with requirements of, the entire study.
  • Have given written consent to participate in the study after reading the ICF, and after having the opportunity to discuss the study with the Investigator or his delegate.
  • Have given written consent to have his/her data entered into The Over volunteering Prevention System.

Exclusion Criteria:

  • Clinically relevant abnormal history, physical findings, ECG findings, or laboratory values that could interfere with the objectives of the study or compromise the safety of the subject.
  • Presence or history of acute or chronic illness, including (but not limited to) liver or kidney disease, hypertension, seizures, or any known impairment of endocrine, or other specific body-organ dysfunction.
  • History of serious reaction to any medicine.
  • Presence or history of malignant disease.
  • Acute or chronic infectious disease, including human immunodeficiency virus (HIV), hepatitis B virus (HBV) or C virus (HCV) infection.
  • Surgery (eg, stomach bypass) or medical condition that might affect how the body handles or absorbs medicines.
  • Significant illness within 4 weeks before the first dose of study medication.
  • Participation in another clinical study of a new chemical entity or a prescription medicine within the previous 3 months, or unwilling to abstain from participating in other clinical trials during the study and for 3 months after receipt of study medication.
  • Blood pressure (BP) and heart rate in semi-supine position at the Screening examination outside the ranges 90 mmHg to 140 mmHg systolic, 40 mmHg to 90 mmHg diastolic; heart rate < 40 beats/min to > 100 beats/min. Subjects with Stage 1 hypertension (systolic 140 mmHg to 160 mmHg; diastolic 90 mmHg to 100 mmHg) may be enrolled provided they do not have evidence of end-organ damage, diabetes or a 10 year cardiovascular risk > 20%.
  • Abnormal ECG waveform morphology at Screening that would preclude accurate measurement of the uncorrected QT interval (QT) duration.
  • QT interval for heart rate corrected using QTcF interval duration > 430 ms for men or > 450 ms for women, obtained as an average from the measurements on duplicate Screening ECGs over a brief recording period.
  • Estimated glomerular filtration rate (eGFR) < 80 mL/min/1.73m2 (based on Modification of Diet in Renal Disease [MDRD] equation) or an absolute creatinine value outside the normal range.
  • Use of any prescription or over the counter (OTC) medications, or herbal remedies (such as St John's wort), known to be strong inhibitors or strong inducers of cytochrome (CYP) enzymes (also known as CYP P450 enzymes) during the 30 days before the first dose of study medication; use of any other prescription or OTC medicine (with the exception of acetaminophen (paracetamol)), including dietary supplements or herbal remedies, during the 7 days before the dose of study medication.
  • Pregnant or breastfeeding women.
  • Consumption of certain foods or beverages before the first dose and throughout the study period.
  • Loss of more than 400 mL blood or donation of blood, plasma, platelets, or any other blood components during the 3 months before the first dose of study medication, or unwilling to abstain from doing so during the study and for 3 months after receipt of study medication.
  • Abuse of drugs or alcohol during the 2 years before the first dose of study medication, or intake of more than 21 units of alcohol weekly for male subjects and 14 units of alcohol weekly for female subjects.
  • Use of tobacco products or nicotine-containing products during the 3 months before the first dose of study medication and during the study.
  • Evidence of drug or alcohol abuse at screening or admission.
  • Likely possibility that the volunteer will not cooperate with the requirements of the protocol.
  • Objection by General Practitioner (GP) to the volunteer entering the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 기초 과학
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: DS-1971a (Low Dose)
Participants in Cohort 1 who receive a low dose of DS 1971a in an oral suspension
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
실험적: DS-1971a (Mid dose)
Participants in Cohort 2 who receive a mid dose of DS 1971a in an oral suspension
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
실험적: DS-1971a (High dose)
Participants in Cohort 3 who receive a high dose of DS 1971a in an oral suspension
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
실험적: Pooled placebo
Participants in Cohort 1, 2 or 3 who receive matching DS-1971a Placebo
Placebo matching DS-1971a suspension

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Number of participants with at least one Treatment Emergent Adverse Event (TEAEs)
기간: 14 days
TEAEs are adverse events that began or got worse after treatment began. Clinically significant changes in laboratory tests and/or physical examinations are considered adverse events.
14 days

2차 결과 측정

결과 측정
측정값 설명
기간
Cmax of DS-1971a
기간: Day 1 and Day 14
Cmax is the highest concentration of the drug in the blood
Day 1 and Day 14
Tmax of DS-1971a
기간: Day 1 and Day 14
Tmax is the time it takes for Cmax to be reached
Day 1 and Day 14
Area Under Curve at steady state (AUCtau) of DS-1971a
기간: Day 1 and Day 14
AUCtau is the area under the plasma concentration-time curve at steady state. In pharmacokinetics, steady state refers to the situation where the overall intake of a drug is about even with the rate it is being eliminated from the body.
Day 1 and Day 14
Area under the Curve (additional measures) for DS-1971a
기간: Day 1 and Day 14
Additional AUC measures include AUC0-24 (to 24 hours), AUClast (to the last observable measure), AUC0-inf (to infinity), and AUCextr (from AUClast to infinity)
Day 1 and Day 14
Tmax of DS-1971a metabolites M1 and M2
기간: Day 1 and Day 14
Tmax of metabolites M1 and M2 characterized by Tmax
Day 1 and Day 14
Cmax of DS-1971a metabolites M1 and M2
기간: Day 1 and Day 14
Cmax of metabolites M1 and M2 characterized by Cmax
Day 1 and Day 14
AUC of DS-1971a metabolites M1 and M2
기간: Day 1 and Day 14
AUC measures include AUCtau, AUC0-24, AUClast, AUC0-inf
Day 1 and Day 14

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2015년 9월 1일

기본 완료 (실제)

2015년 12월 1일

연구 완료 (실제)

2015년 12월 1일

연구 등록 날짜

최초 제출

2015년 9월 28일

QC 기준을 충족하는 최초 제출

2015년 9월 29일

처음 게시됨 (추정)

2015년 10월 1일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 4월 28일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 4월 27일

마지막으로 확인됨

2017년 4월 1일

추가 정보

이 연구와 관련된 용어

키워드

기타 연구 ID 번호

  • DS1971-A-E106
  • 2015-002885-22 (EudraCT 번호)

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

DS-1971a에 대한 임상 시험

3
구독하다