drugset / Trial / NCT04566601

A Study to Test Different Doses of BI 1358894 and Find Out Whether They Reduce Symptoms in People With Borderline Personality Disorder

NCT04566601

Phase 2 Completed 390 enrolled Boehringer Ingelheim
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is open to adults with borderline personality disorder. The purpose of this study is to find out whether a medicine called BI 1358894 helps to reduce symptoms in people with borderline personality disorder. Four different doses of BI 1358894 are tested in the study. Participants are put into 5 groups by chance. Participants in 4 of the 5 groups take different doses of BI 1358894. Participants in the fifth group take placebo. Participants take BI 1358894 and placebo as tablets once a day. Placebo tablets look like BI 1358894 tablets but do not contain any medicine. Participants are in the study for about 5 months. During this time, they visit the study site about 12 times and get about 6 phone calls. At the visits, doctors ask participants about their symptoms. The results between the BI 1358894 groups and the placebo group are then compared. The doctors also regularly check the general health of the participants.

Timeline

Start
2020-11-13
Primary completion
2022-12-09
Completion
2023-01-25

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1358894 Small molecule 5 mg
Subject BI 1358894 Small molecule 25 mg
Subject BI 1358894 Small molecule 75 mg
Subject BI 1358894 Small molecule 125 mg