Safety, Tolerability, Pharmacokinetics and Early Pharmacodynamics of Single Rising Oral Doses of BI 1021958 Tablets in Healthy Male Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

February 29, 2012

Primary Completion Date

May 31, 2012

Conditions
Healthy
Interventions
DRUG

BI 1021958

tablet

DRUG

BI 1021958

drinking solution / tablet

DRUG

Placebo to BI 1021958

SRD part: oral administration in fasted state, FE part: oral administration in fasted state and after standard high fat breakfast

Trial Locations (1)

Unknown

1310.1.1 Boehringer Ingelheim Investigational Site, Biberach

Sponsors
All Listed Sponsors
lead

Boehringer Ingelheim

INDUSTRY