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

PHASE1CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

November 16, 2016

Primary Completion Date

December 22, 2016

Study Completion Date

March 17, 2017

Conditions
Pharmacokinetics
Interventions
DRUG

Finerenone (BAY94-8862): 1 0mg tablet

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

DRUG

Finerenone (BAY94-8862): 5 X 0.25 mg oro-dispersible tablets

5 x 0.25 mg (1.25 mg) oro-dispersible tablets; single dose in the fasting condition

DRUG

Finerenone (BAY94-8862): 1.25 mg oro-dispersible tablet

1.25 mg finerenone oro-dispersible tablets; single dose in the fasting condition or in the fed condition

Trial Locations (1)

41061

Mönchengladbach

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY