Safety, Tolerance, and Pharmacokinetics of Single Rising Oral Doses of BILB 1941 ZW Solution in Healthy Male Subjects, Followed With Bioavailability Comparison of BILB 1941 ZW Tablet and Solution Formulation Administered With or Without Food
Safety, Tolerance, and Pharmacokinetics of Single Oral Doses of 5 mg, 20 mg, 60 mg, 120 mg, 200 mg, 300 mg, 600 mg, 1000 mg, 1500 mg, 2000 mg, 2400 mg, and 3000 mg BILB 1941 ZW (PEG 400/TRIS Solution) in Healthy Male Subjects, in a Randomised Double Blind, Placebo Controlled Rising Dose Study, Followed With an Open-label Intra-subject Three-Way Crossover Bioavailability Comparison of 600 mg BILB 1941 ZW in a PEG 400/TRIS Solution and 600 mg BILB 1941 ZW Tablet and 600 mg BILB 1941 ZW Tablet Administered With Food
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
등록 (실제)
등록
단계
단계
- 1단계
참여기준
자격 기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
Healthy males according to the following criteria based upon a complete medical history, including the physical examination, vital signs (BP, PR), 12-lead ECG, clinical laboratory tests:
1.1 No finding deviating from normal and of clinical relevance
1.2 No evidence of a clinically relevant concomitant disease
- Age ≥18 and Age ≤50 years, BMI ≥18.5 and BMI ≤29.9 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice (GCP) and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
- History or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, hormonal disorders, including a clinical history of viral hepatitis, or serological evidence of active Hepatitis B or Hepatitis C infection
- History of orthostatic hypotension, fainting spells and blackouts
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
- Intake of drugs with a long half-life (> 24 hours) within 1 month prior to administration
- Use of any drugs which might influence the results of the trial within 10 days prior to administration or during the trial
- Participation in another trial with an investigational drug within 1 month prior to administration or during the trial
- Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on trial days
- Alcohol abuse (> 60 g/day)
- Drug abuse
- Blood donation of more than 100 mL within 1 month prior to administration or during the trial
- Excessive physical activities within 5 days prior to administration or during the trial
- Any laboratory value outside the clinically accepted reference range and of clinical relevance
- History of any familial bleeding disorder
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
실험적: BILB 1941 ZW - single rising dose
Single rising dose part
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위약 비교기: Placebo
Single rising dose part
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실험적: BILB 1941 ZW - tablet - fasted
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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실험적: BILB 1941 ZW - solution
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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실험적: BILB 1941 ZW - tablet - fed
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Number of subjects with abnormal findings in physical examination
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
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Number of subjects with abnormal changes in laboratory parameters
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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Number of subjects with clinically significant changes in vital signs
기간: up to 48 hours following drug administration
|
Blood pressure, Pulse Rate
|
up to 48 hours following drug administration
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Number of subjects with adverse events
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
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Number of subjects with clinically significant changes in 12-lead ECG (electrocardiogram)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
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Assessment of tolerability by investigator on a 4-point scale
기간: after 48 hours following drug administration
|
after 48 hours following drug administration
|
2차 결과 측정
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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tmax (time from dosing to maximum concentration)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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λz (terminal rate constant in plasma)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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t1/2 (terminal half-life of the analyte in plasma)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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MRT (Mean time of residence of drug molecules in the body after intravascular administration)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
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Vz/F (Apparent volume of distribution during the terminal phase after extravascular administration)
기간: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
공동 작업자 및 조사자
간행물 및 유용한 링크
유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작
연구 시작
기본 완료 (실제)
기본 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
기타 연구 ID 번호
- 1201.1
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