Study to Investigate the Natriuretic Effects, Safety, Tolerability and Pharmacokinetics of BAY94-8862

PHASE1CompletedINTERVENTIONAL
Enrollment

67

Participants

Timeline

Start Date

March 29, 2010

Primary Completion Date

November 30, 2010

Study Completion Date

May 17, 2011

Conditions
Clinical Pharmacology
Interventions
DRUG

Finerenone (BAY 94-8862) PEG solution

2.5, 5, 10, 20 mg polyethylene glycol (PEG) solution of BAY 94-8862

DRUG

Finerenone (BAY 94-8862) immediate release tablet

20 mg BAY 94-8862 administered as 2 x 10 mg IR tablets

DRUG

Eplerenone (Inspra®)

Single oral dose of 50 mg eplerenone

DRUG

Placebo

Matching placebo (solution/tablet) corresponding to BAY 94-8862 dose in respective dose step

Trial Locations (1)

41460

Neuss

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY