A Study to Evaluate the Effects of 4 Weeks Treatment With Subcutaneous Elamipretide on Left Ventricular Function in Subjects With Stable Heart Failure With Preserved Ejection Fraction

PHASE2CompletedINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

September 2, 2016

Primary Completion Date

May 4, 2017

Study Completion Date

June 2, 2017

Conditions
Chronic Heart Failure
Interventions
DRUG

elamipretide

Subcutaneous injection of 40 mg elamipretide once daily for 28 consecutive days

DRUG

Placebo

Subcutaneous injection of placebo administered once daily for 28 consecutive days

Trial Locations (9)

11000

Clinical Centre of Serbia, Clinic for Cardiology, Belgrade

"Clinical Hospital Center Dr Dragiša Mišović-Dedinje, Department of Cardiology", Belgrade

"Clinical Hospital Center Zvezdara, Department of Cardiology", Belgrade

11080

"Clinical Hospital Center Bežanijska Kosa, Department of Cardiology", Belgrade

"Clinical Hospital Center Zemun, Department of Cardiology", Belgrade

13353

Charite Universitatsmedizin Berlin, Campus Virchow-Klinikum, Berlin

German Heart Center, Berlin

18000

Clinical Center Niš, Clinic for Cardiology, Niš

21204

Institute for Cardiovascular Diseases Vojvodina, Clinic for Cardiology, Kamenitz

All Listed Sponsors
collaborator

Charite University, Berlin, Germany

OTHER

collaborator

SCIRENT Clinical Research and Science d.o.o.

UNKNOWN

lead

Stealth BioTherapeutics Inc.

INDUSTRY

NCT02814097 - A Study to Evaluate the Effects of 4 Weeks Treatment With Subcutaneous Elamipretide on Left Ventricular Function in Subjects With Stable Heart Failure With Preserved Ejection Fraction | Biotech Hunter | Biotech Hunter