Phase IIb Safety and Efficacy Study of BAY94-8862 in Subjects With Worsening Chronic Heart Failure and Left Ventricular Systolic Dysfunction and Either Type 2 Diabetes Mellitus With or Without Chronic Kidney Disease or Moderate Chronic Kidney Disease Alone

PHASE2CompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

November 11, 2013

Primary Completion Date

January 23, 2015

Study Completion Date

February 20, 2015

Conditions
Heart Failure
Interventions
DRUG

BAY94-8862

2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, and 20 mg of BAY94-8862 tablets

DRUG

Eplerenone

INSPRA 25 and 50 mg tablets (MAH: Pfizer) will be used for eplerenone 25 and 50 mg tablets

DRUG

Placebo

matching placebo

Trial Locations (29)

489-8642

Seto

471-8513

Toyota

273-8588

Funabashi

296-8602

Kamogawa

790-0067

Matsuyama

818-8516

Chikushino-shi

660-8550

Amagasaki

650-0047

Kobe

654-0155

Kobe

311-3193

Higashiibaraki

254-8502

Hiratsuka

211-8533

Kawasaki

245-8575

Yokohama

611-0041

Uji

983-8520

Sendai

900-0005

Naha

902-8511

Naha

901-2132

Urasoe

350-1305

Sayama

525-8585

Kusatsu

162-8655

Shinjuku-ku

162-8666

Shinjuku-ku

400-8506

Kofu

810-0001

Fukuoka

892-0853

Kagoshima

607-8062

Kyoto

700-8607

Okayama

558-8558

Osaka

420-8630

Shizuoka

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY