Study of Finerenone to Investigate a Paediatric Formulation in Healthy Male Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

November 17, 2016

Primary Completion Date

January 13, 2017

Study Completion Date

March 1, 2017

Conditions
Pharmacokinetics
Interventions
DRUG

Finerenone (BAY94-8862): 20 mg intact tablet

20 mg intact finerenone immediate-release tablet; single dose in the fasting condition

DRUG

Finerenone (BAY94-8862): 20 mg crushed and resuspended tablet

20 mg crushed and resuspended finerenone immediate-release tablet; single dose in the fasting condition

DRUG

Finerenone (BAY94-8862): 20 mg suspension

20 mg finerenone suspension; single dose in the fasting condition or in the fed condition

Trial Locations (1)

13353

Berlin

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY

NCT02957396 - Study of Finerenone to Investigate a Paediatric Formulation in Healthy Male Subjects | Biotech Hunter | Biotech Hunter