Safety, tolerability and pharmacokinetics of single rising oral doses and multiple oral doses of BI 1569912 in healthy male Japanese subjects (single-blind, partially randomized within dose groups, placebocontrolled, parallel-group design)

Nippon Boehringer Ingelheim Co., Ltd.0 个研究点目标入组 44 人开始时间: 待定最近更新: 2024年4月18日

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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 (BP, PR), 12-lead
•ECG, and clinical laboratory tests
•Japanese ethnicity
•BMI of 18.5 to 25.0 kg/m2 (inclusive)
•Signed and dated written informed consent prior to admission to the study, in accordance
•with GCP and local legislation

•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 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

the percentage [%] of subjects with drug-related AEs per treatment group

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