There is one clinical trial.
The main objectives of this trial are to investigate safety, tolerability and
pharmacokinetics (PK) of BI 474121 in healthy male subjects following oral administration of
single rising doses.
Primary Outcomes
Measure: Percentage of subjects with drug-related adverse events (Single-rising dose (SRD) part) Time: Up to 15 days
Measure: BA part: AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point) Time: Up to 96 hours
Measure: BA part: Cmax (maximum measured concentration of the analyte in plasma) Time: Up to 96 hours
Secondary Outcomes
Measure: SRD part: AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point) Time: Up to 96 hours
Measure: SRD part: Cmax (maximum measured concentration of the analyte in plasma) Time: Up to 96 hours
Measure: BA part: AUC0-∞ (area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity) Time: Up to 96 hours