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Recombinant Human Alkaline Phosphatase in Healthy Japanese Subjects

2022년 3월 11일 업데이트: AM-Pharma

A Double Blind, Randomized, Single Center, Single and Multiple Dose, Pharmacokinetic, Safety and Tolerability Study of Recombinant Human Alkaline Phosphatase (recAP) Administered Intravenously in Healthy Japanese Subjects

Clinical Phase 1 study to investigate the pharmacokinetics and to assess the safety and tolerability of recAP after single and multiple intravenous doses in healthy Japanese subjects.

연구 개요

상세 설명

This study is a randomized, double blind, parallel group, single-center trial, consisting of a single dose part and a multiple dose part in 32 healthy Japanese subjects. Since all these doses have been studied before and safety extensively evaluated in non-Japanese subjects and no ethnic sensitivity is expected, the groups can be dosed in parallel.

Part A will have 3 parallel groups of 8 male subjects with N=6 on active and N=2 on placebo per group. Following baseline assessments, a single dose of recAP will be administered by a one-hour infusion followed by samplings for pharmacokinetic evaluation and routine safety assessments.

Part B will have a single group of 8 male subjects with N=6 on active and N=2 on placebo. Following baseline assessments, recAP will be dosed on Days 1, 2 and 3 by one-hour infusions followed by samplings for pharmacokinetic evaluation and routine safety assessments.

연구 유형

중재적

등록 (실제)

34

단계

  • 1단계

연락처 및 위치

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

연구 장소

      • Tokyo, 일본, 192-0071
        • P-One Clinic, Keikokai Medical Corporation

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

20년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

남성

설명

Inclusion Criteria:

  1. Gender : male
  2. Age : 20-55 years, inclusive
  3. Body mass index (BMI) : 18.0-30.0 kg/m2, inclusive
  4. Subjects must be Japanese by birth, have resided outside Japan <10 years, have parents and maternal and paternal grandparents who are Japanese, and primarily consume a Japanese diet.
  5. Resting supine blood pressure at screening showing no clinically relevant deviations from normal as judged by the Principal Investigator.
  6. Computerized (12-lead) ECG recording without signs of clinically relevant pathology or showing no clinically relevant deviations.
  7. All values for hematology and for clinical chemistry tests of blood and urine within the normal range or showing no clinically relevant deviations as judged by the Investigator.
  8. Ability and willingness to abstain from alcohol and tobacco products from 48 h prior to entry in the clinical research center until discharge.
  9. Easily accessible veins for venipuncture and catheter placing.
  10. Willingness to sign the written informed consent form (ICF).
  11. Subjects must agree to use adequate contraception when sexually active. This applies for the time period between end of first administration and 14 days after the last administration of study drug.

Exclusion Criteria:

  1. Evidence of clinically relevant pathology.
  2. History of relevant drug and/or food allergies.
  3. Subject has a history of clinically significant abnormalities or of any illness that, in the opinion of the study investigator, might confound the results of the study or poses an additional risk to the subject by their participation in the study.
  4. Use of medication, except for acetaminophen (paracetamol), which is allowed up to 3 days before entry into the clinical research center (after that time the use of a limited amount of acetaminophen is permitted after consultation with the Principal Investigator).
  5. Subject is mentally or legally incapacitated, has significant emotional problems at the time of screening visit or expected during the conduct of the study or has a history of a clinically significant psychiatric disorder over the last year.
  6. Participation in a drug study within 60 days prior to drug administration.
  7. Donation of more than 500 mL of blood within 60 days prior to drug administration. Donation of more than 1.5 liters of blood (for men) in the 10 months preceding the start of this study
  8. Smoking more than 5 cigarettes, 1 cigar or 1 pipe daily.
  9. History of alcohol abuse or drug addiction (including soft drugs like cannabis products).
  10. Positive drug screen (opiates, methadone, cocaine, amphetamines, cannabinoids, barbiturates, benzodiazepines, tricyclic antidepressants) and/or alcohol breath test at Screening and/or Pre-Dose.
  11. Intake of more than 14 units of alcohol per week (one unit of alcohol equals approximately 250 mL of beer, 100 mL of wine/Japanese Sake or 35 mL of spirits).
  12. Positive screen on hepatitis B surface antigen (HBsAg), anti-hepatitis C virus (anti-HCV) or anti-human immunodeficiency virus (anti-HIV)-1 or anti-HIV-2 or HIV-1/2 antigen.
  13. Illness within 5 days prior to (the first) drug administration.

공부 계획

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

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 순차적 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: Group 1: single 1-hour IV infusion of 0.8 mg/kg recAP or placebo
single 1-hour IV infusion of 0.8 mg/kg recAP or placebo
Intravenous infusion
Intravenous infusion
활성 비교기: Group 2: single 1-hour IV infusion of 1.6 mg/kg recAP or placebo
single 1-hour IV infusion of 1.6 mg/kg recAP or placebo
Intravenous infusion
Intravenous infusion
활성 비교기: Group 3: single 1-hour IV infusion of 3.2 mg/kg recAP or placebo
single 1-hour IV infusion of 3.2 mg/kg recAP or placebo
Intravenous infusion
Intravenous infusion
활성 비교기: Group 4: 1-hour infusions of 1.6 mg/kg recAP or placebo on Days 1, 2 and 3
1-hour infusions of 1.6 mg/kg recAP or placebo on Days 1, 2 and 3
Intravenous infusion
Intravenous infusion

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Maximum observed recAP plasma concentration (Cmax) after single dose
기간: Single dose 9 days treatment phase
Blood collection for cmax evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
Time to attain maximum recAP serum concentration (Tmax) after single dose
기간: Single dose 9 days treatment phase
Blood collection for Tmax evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
Area under the plasma concentration versus time curve (AUC) after single dose
기간: Single dose 9 days treatment phase
Blood collection for AUC evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
recAP elimination half-life ( t1/2) after single dose
기간: Single dose 9 days treatment phase
Blood collection for t1/2 evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
Maximum observed recAP plasma concentration (Cmax) after multiple doses
기간: Multiple doses 13 days treatment phase
Blood collection for cmax evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase
Time to attain maximum recAP serum concentration (Tmax) after multiple doses
기간: Multiple doses 13 days treatment phase
Blood collection for Tmax evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase
Area under the plasma concentration versus time curve (AUC) after multiple doses
기간: Multiple doses 13 days treatment phase
Blood collection for AUC evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase
recAP elimination half-life ( t1/2) after multiple doses
기간: Multiple doses 13 days treatment phase
Blood collection for t1/2 evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase

2차 결과 측정

결과 측정
측정값 설명
기간
Adverse events (AEs) after single dose
기간: Single dose 9 days treatment phase
Any untoward medical occurrence in a subject enrolled into a clinical study regardless of its causal relationship to study drug.
Single dose 9 days treatment phase
Adverse events (AEs) after multiple doses
기간: Multiple doses 13 days treatment phase
Any untoward medical occurrence in a subject enrolled into a clinical study regardless of its causal relationship to study drug.
Multiple doses 13 days treatment phase

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 연구 책임자: Annelies Legters, AM-Pharma

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 (실제)

2021년 5월 7일

기본 완료 (실제)

2021년 7월 8일

연구 완료 (실제)

2021년 12월 31일

연구 등록 날짜

최초 제출

2021년 5월 25일

QC 기준을 충족하는 최초 제출

2021년 6월 9일

처음 게시됨 (실제)

2021년 6월 11일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2022년 3월 14일

QC 기준을 충족하는 마지막 업데이트 제출

2022년 3월 11일

마지막으로 확인됨

2022년 3월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • AP-recAP-AKI-01-02

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

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약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

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미국 FDA 규제 기기 제품 연구

아니

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. .

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