- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03492931
PK Study of Ticagrelor in Children Aged Less Than 24 Months, With Sickle Cell Disease (HESTIA4) (HESTIA4)
A Multi-centre, Phase I, Open-label, Single-dose Study to Investigate Pharmacokinetics (PK) of Ticagrelor in Infants and Toddlers, Aged 0 to Less Than 24 Months, With Sickle Cell Disease (HESTIA4)
The purpose of this Phase I study is to investigate the pharmacokinetic properties of ticagrelor in pediatric patients from 0 to less than 24 months with sickle cell disease.
Ticagrelor dose level adjustment will require a Protocol amendment and regulatory approval.
연구 개요
상세 설명
Study design This Phase I paediatric study (in patients aged 0 to <24 months) with ticagrelor is planned to be a multi-centre, open-label, single dose study.
Primary Objective:
To determine the PK properties of ticagrelor after a single oral dose
Secondary Objectives:
To determine the PK properties of the active metabolite (AR-C124910XX) after a single oral dose To assess the acceptability and the palatability of a single oral dose of ticagrelor
Safety Objective:
To assess safety and tolerability of a single oral dose of ticagrelor
Duration of treatment At least 20 eligible patients will receive a single open label oral dose of ticagrelor on Day 1.
Statistical methods A population PK analysis approach will be used to determine the PK parameters of ticagrelor and its metabolite AR-C124910XX in paediatric patients aged 0 to <24 months eg, CL/F (oral clearance) (only for ticagrelor) and AUC.
The PK will also be described by presenting the observed plasma concentrations of Ticagrelor and its active metabolite for all individuals, as well as corresponding descriptive statistics.
No statistical comparisons are planned for the primary or secondary objectives, which will be summarised descriptively
연구 유형
등록 (실제)
단계
- 1단계
연락처 및 위치
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Paediatric patients aged <24 months, diagnosed with homozygous sickle cell (HbSS) or sickle beta-zero-thalassemia (HbS/β0), as confirmed by high performance liquid chromatography or haemoglobin electrophoresis.
- Body weight ≥5 kg at the time of screening.
- If treated with an anti-sickling agent such as hydroxyurea, the weight-adjusted dose must be stable for 3 months before screening/enrolment.
- Provision of signed and dated written informed consent from parents/legal guardians prior to any study specific procedures not part of standard medical care.
Exclusion criteria
- History of transient ischaemic attack or cerebrovascular event/accident (ischaemic or haemorrhagic), severe head trauma, intracranial haemorrhage, intracranial neoplasm, arteriovenous malformation, aneurysm, or proliferative retinopathy.
- Significantly underdeveloped with regards to height, weight or head circumference for age, as judged by the Investigator.
- Severe developmental delay (eg, cerebral palsy or mental retardation).
- Receiving chronic treatment (>3 days/week) with non-steroidal anti-inflammatory drugs (NSAIDs).
- Receiving chronic treatment with anticoagulants or antiplatelet drugs that cannot be discontinued.
- Moderate or severe hepatic impairment, defined as laboratory values of alanine aminotransferase (ALT) >2 × upper limit of normal (ULN), total bilirubin >2 × ULN (unless judged by the Investigator to be caused by haemolysis), albumin <35 g/L and international normalised ratio (INR) >1.4, or symptoms of liver disease (eg, ascites).
- Renal failure requiring dialysis.
- Active pathological bleeding or increased risk of bleeding complications according to the Investigator.
- Haemoglobin <6 g/dL from test performed at Screening (Visit 1).
- Platelets <100 × 10^9/L from test performed at Screening (Visit 1).
- Patient considered to be at risk of bradycardic events (eg, known sick sinus syndrome or second or third degree atrioventricular block).
- Concomitant oral or intravenous therapy with moderate or strong CYP3A4 inhibitors, CYP3A4 substrates with narrow therapeutic indices, or strong CYP3A4 inducers that have not been stopped at least 5 half-lives before dose administration.
- Patient breastfed by mother who is under treatment of strong CYP3A4 inhibitors,
- Active untreated malaria. Patients with suspected malaria at Screening (Visit 1) will be tested.
- Surgical procedure planned to occur during the study including 5 days after ticagrelor administration.
- Known hypersensitivity or contraindication to ticagrelor.
- Concern for the inability of the patient or parents to comply with study procedures and/or follow-up.
- Any condition which, in the opinion of the Investigator, would make it unsafe or unsuitable for the patient to participate in this study.
- Previously administered ticagrelor in the present study.
- Participation in another clinical study with an investigational medicinal product (IMP) or device during the last 30 days preceding screening/enrolment.
- Involvement of member of patient's family in planning and/or conduct of the study (applies to both AstraZeneca personnel and personnel at study centre).
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Treatment arm
Single dose of ticagrelor based on age
|
Patients will receive a single dose of ticagrelor
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Peak Plasma Concentration (Cmax) of Ticagrelor
기간: 1,2,4,6 hours post dose
|
This measure is obtained from observed plasma concentrations
|
1,2,4,6 hours post dose
|
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Area under plasma concentration curve
기간: 1,2,4,6 hours post dose
|
This measure is obtained from the population PK analysis
|
1,2,4,6 hours post dose
|
|
CL/F (Oral clearance)
기간: 1,2,4,6 hours post dose
|
This measure is obtained from the population PK analysis.
|
1,2,4,6 hours post dose
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Peak Plasma Concentration (Cmax) for active metabolite (AR-C124910XX)
기간: 1,2,4,6 hours post dose
|
1,2,4,6 hours post dose
|
|
|
Area under plasma concentration curve
기간: 1,2,4,6 hours post dose
|
1,2,4,6 hours post dose
|
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Assessment of ticagrelor suspension for palatability
기간: Day 1, single timepoint assessment
|
Questionnaire with one five-options question reflecting different degrees of patients willingness to swallow, from "swallowed without problem" to "vomited up medication".
|
Day 1, single timepoint assessment
|
공동 작업자 및 조사자
스폰서
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- D5136C00010
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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