Dose Escalation Study to Investigate Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of BAY85-3934 in Subjects With Chronic Kidney Disease (CKD)

PHASE1CompletedINTERVENTIONAL
Enrollment

49

Participants

Timeline

Start Date

September 30, 2012

Primary Completion Date

February 28, 2013

Study Completion Date

July 31, 2013

Conditions
Kidney Diseases
Interventions
DRUG

Molidustat (BAY85-3934)

20 mg molidustat as a single tablet

DRUG

Placebo

Single oral dose of matching placebo will be given in each treatment arm

Trial Locations (3)

24105

Kiel

41061

Mönchengladbach

81241

München

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY

NCT01679587 - Dose Escalation Study to Investigate Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of BAY85-3934 in Subjects With Chronic Kidney Disease (CKD) | Biotech Hunter | Biotech Hunter