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临床试验/JPRN-jRCT2071230092
JPRN-jRCT2071230092招募中1 期

Pharmacokinetics of R-BI 1015550 after single oral doses ofBI 1015550 in Japanese healthy male subjects (open-label, nonrandomised,and parallel group design)

Mochizuki Toko0 个研究点目标入组 12 人开始时间: 2023年11月21日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 <= 45age old(—)
性别
Male

入选标准

  • Healthy male subjects, age of 18 to 45 years (inclusive), body mass index (BMI)
  • of 18.5 to 25.0 kg/m2 (inclusive)

排除标准

  • -Any finding in the medical examination (including BP, PR, RR 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 PR 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
  • -Any documented active or suspected malignancy or history of malignancy within 5 years
  • prior to screening, except appropriately treated basal cell carcinoma or in situ squamous
  • cell carcinoma of the skin or in situ carcinoma of uterine cervix
  • -Inability to comply with the dietary regimen of the trial site
  • -A marked prolongation of QT/QTc interval (such as QTc intervals that are repeatedly
  • greater than 450 ms in male) or any other relevant ECG finding at screening.
  • -A history of additional risk factors for Torsade de Pointes (such as heart failure,
  • hypokalaemia, or family history of Long QT Syndrome)
  • -Any lifetime history of suicidal behavior (i.e. actual attempt, interrupted attempt, aborted
  • attempt, or preparatory acts or behavior)
  • -History of vasculitis

研究者

发起方
Mochizuki Toko

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