A Study in Healthy Japanese Men to Test How Different Doses of BI 1569912 Are Taken up by the Body and How Well They Are Tolerated
- Registration Number
- NCT04958252
- Lead Sponsor
- Boehringer Ingelheim
- Brief Summary
The main objectives of this trial are to investigate safety and tolerability of BI 1569912 in healthy male Japanese subjects following oral administration of single rising doses and multiple doses.
Secondary objective is the exploration of pharmacokinetics (PK) of BI 1569912.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- Male
- Target Recruitment
- 56
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Healthy male subjects according to the assessment of the investigator, as based on a complete medical history including a medical examination, vital signs (blood pressure (BP), pulse rate (PR)), 12-lead Electrocardiogram (ECG), and clinical laboratory tests
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Japanese ethnicity, according to the following criteria: born in Japan, have lived outside of Japan <10 years, and have parents and grandparents who are Japanese
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Age of 18 to 45 years (inclusive)
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Body mass index (BMI) of 18.5 to 25.0 kg/m2 (inclusive)
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Signed and dated written informed consent prior to admission to the study, in accordance with Good Clinical Practice (GCP) and local legislation
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Subjects who agree to minimize the risk of making their partner pregnant by fulfilling any of the following criteria starting from the first administration of trial medication until 90 days after last administration of trial medication
- Use of adequate contraception, any of the following methods plus condom: intrauterine device, combined oral contraceptives that started at least 2 months prior to the first drug administration.
- Vasectomized (vasectomy at least 1 year prior to enrolment)
- Surgical sterilization (including bilateral tubal occlusion, hysterectomy or bilateral oophorectomy) of the subject's female partner
- Any finding in the medical examination (including BP, PR or ECG) deviating from normal and assessed as clinically relevant by the investigator
- Repeated measurement of systolic blood pressure outside the range of 90 to 140 mmHg, diastolic blood pressure outside the range of 40 to 90 mmHg, or pulse rate outside the range of 40 to 99 beats per minute (bpm)
- Any laboratory value outside the reference range that the investigator considers to be of clinical relevance
- Any evidence of a concomitant disease assessed as clinically relevant by the investigator
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Cholecystectomy or other surgery of the gastrointestinal tract that could interfere with the pharmacokinetics of the trial medication (except appendectomy or simple hernia repair)
- Diseases of the central nervous system (including but not limited to any kind of seizures or stroke), and other relevant neurological or psychiatric disorders
- History of relevant orthostatic hypotension, fainting spells, or blackouts Further exclusion criteria apply.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Placebo Placebo - Part A: BI 1569912 low dose BI 1569912 - Part A: BI 1569912 lower medium dose BI 1569912 - Part A: BI 1569912 higher medium dose BI 1569912 - Part A: BI 1569912 high dose BI 1569912 - Part B: BI 1569912 low dose BI 1569912 - Part B: BI 1569912 high dose BI 1569912 - Part C: BI 1569912 BI 1569912 -
- Primary Outcome Measures
Name Time Method Part A and Part B: Percentage of subjects with drug-related adverse events up to 27 days Part C: Maximum measured concentration of the analyte in plasma (Cmax) up to 3 days Part C: Area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point (AUC0-tz) up to 3 days
- Secondary Outcome Measures
Name Time Method Part A: Area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity (AUC0-∞) up to 4 days Part A: Maximum measured concentration of the analyte in plasma (Cmax) up to 4 days Part B, after the first dose: Area under the concentration-time curve of the analyte in plasma from 0 to 24 hours (AUC0-24) up to 17 days Part B, after the first dose: Maximum measured concentration of the analyte in plasma (Cmax) up to 17 days Part B, after the last dose: Area under the concentration-time curve of the analyte in plasma over the dosing interval τ at steady state (AUCτ,ss) up to 17 days Part B, after the last dose: Maximum measured concentration of the analyte in plasma at steady state (Cmax,ss) up to 17 days Part C: Percentage of subjects with drug-related adverse events up to 3 days Part C: Area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity (AUC0-∞) up to 3 days
Trial Locations
- Locations (1)
SOUSEIKAI Sumida Hospital
🇯🇵Tokyo, Sumida-ku, Japan