跳至主要内容
临床试验/NCT02194348
NCT02194348
已完成
1 期

A Double-blind (Within Dose Groups), Randomized, Placebo-controlled Single Increasing Dose Tolerability Study (Parallel Groups) in Healthy Male and Female Volunteers After Subcutaneous Administration of BIBN 4096 (Dosage: 2.5 - 30 mg)

Boehringer Ingelheim0 个研究点目标入组 12 人2000年2月

概览

阶段
1 期
干预措施
Placebo
疾病 / 适应症
Healthy
发起方
Boehringer Ingelheim
入组人数
12
主要终点
Number of patients with clinically significant changes in 12-lead Electrocardiogram (ECG)
状态
已完成
最后更新
11年前

概览

简要总结

The objective of the present study was to obtain information about safety, tolerability and pharmacokinetics of BIBN 4096 BS after single subcutaneous administration of increasing doses in healthy male and female volunteers

注册库
clinicaltrials.gov
开始日期
2000年2月
结束日期
2000年3月
最后更新
11年前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Participants should be healthy males and females
  • Age range from 21 to 50 years
  • Broca Index: within 20% of their normal weight
  • All female volunteers must use a safe contraception (i.e. oral contraception, spiral, sterilized)
  • All female volunteers must have a negative pregnancy test
  • Prior to admission to the treatment after giving his/her informed consent (in accordance with Good Clinical Practice (GCP) and local legislation) in writing each subject will have his medical history taken and will receive a complete medical examination (incl. blood pressure and pulse rate measurements) as well as a 12-lead ECG within 14 days before the administration of the test substance. Hematopoietic, hepatic and renal function test will be carried out in the laboratory. The subjects will fast for 12 hours before collection of specimens for all laboratory evaluations

排除标准

  • Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  • Diseases of the central nervous system (such as epilepsy) or with psychiatric disorders or neurological disorders
  • History of orthostatic hypotension, fainting spells or blackouts
  • 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 a drug with a long half-life (\>= 24 hours) within ten half-lives of the respective drug before enrolment in the study or during the study
  • Use of any drugs which might influence the results of the trial within two weeks prior to administration or during the trial
  • Participation in another study with an investigational drug within two months prior to administration or during the trial
  • Smoker (\> 10 cigarettes or 3 cigars or 3 pipes/day)

研究组 & 干预措施

Placebo

干预措施: Placebo

BIBN 4096 BS - in single rising doses

干预措施: BIBN 4096 BS - in single rising doses

结局指标

主要结局

Number of patients with clinically significant changes in 12-lead Electrocardiogram (ECG)

时间窗: up to 8 days after treatment day

Number of patients with abnormal changes in laboratory parameters

时间窗: up to 8 days after treatment day

Number of patients with clinically significant changes in vital signs (blood pressure, pulse rate)

时间窗: up to 8 days after treatment day

Number of patients with adverse events

时间窗: up to 24 days

次要结局

  • Cmax (Maximum measured concentration of the analyte in plasma)(up to 48 hours after drug administration)
  • MRT (Mean time of residence of drug molecules in the body)(up to 48 hours after drug administration)
  • AUC0-∞ (Area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)(up to 48 hours after drug administration)
  • Ae (Amount of drug excreted into urine)(up to 48 hours after drug administration)
  • CL(R) (Renal clearance of the analyte in plasma)(up to 48 hours after drug administration)
  • tmax (Time from dosing to the maximum concentration of the analyte in plasma)(up to 48 hours after drug administration)
  • t½ (Terminal half-life of the analyte in plasma)(up to 48 hours after drug administration)
  • CL/F (Apparent clearance of the analyte in plasma following extravascular administration)(up to 48 hours after drug administration)
  • Vz/F (Apparent volume of distribution of the analyte during the terminal phase)(up to 48 hours after drug administration)

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