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Japanese

Nov. 21, 2023

April. 18, 2024

jRCT2071230092

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

A study to test how different doses of BI 1015550 are taken up in
the body of healthy Japanese men

Mochizuki Toko

Boehringer Ingelheim

2-1-1, Osaki, Shinagawa-ku, Tokyo

+81-120-189-779

medchiken.jp@boehringer-ingelheim.com

Yamagami Tomohiro

Boehringer Ingelheim

2-1-1, Osaki, Shinagawa-ku, Tokyo

+81-120-189-779

medchiken.jp@boehringer-ingelheim.com

Complete

Nov. 21, 2023

12

Interventional

non-randomized controlled trial

open(masking not used)

dose comparison control

parallel assignment

treatment purpose

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

-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

18age old over
45age old under

Male

Not applicable

one dose of BI 1015550(9mg or 18mg)

-area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity
-Cmax (maximum measured concentration of the analyte in plasma)

Nippon Boehringer Ingelheim Co., Ltd.
Hakata Clinic Institutional Review Board
6-18, Tenyamachi, Hakata-ku, Fukuoka-shi, Fukuoka 812-0025, Japan, Fukuoka

+81-92-283-7701

Approval

Nov. 10, 2023

No

none

History of Changes

No Publication date
2 April. 18, 2024 (this page) Changes
1 Nov. 21, 2023 Detail