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A Study to Assess the Hemodynamic Effects, Safety, Tolerability, and Pharmacokinetics of Intravenous APD418 in Adult Participants With Heart Failure With Reduced Ejection Fraction
A Study to Assess the Hemodynamic Effects, Safety, Tolerability, and Pharmacokinetics of Intravenous APD418 in Adult Participants With Heart Failure With Reduced Ejection Fraction
TerminatedPhase 2
Sponsor: Pfizer
Conditions: Acute Heart Failure With Reduced Ejection Fraction
Interventions: APD418, APD418, Placebo
Countries: United States, Germany, Greece, Poland, Serbia
The purpose of this study is to evaluate the safety, pharmacokinetics, and effect on cardiac function of intravenous APD418 in adult participants with heart failure with reduced ejection fraction (HFrEF).
Eligibility overview
Sex: ALL
Age: 18 Years to 85 Years
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * Advanced chronic Heart Failure with Reduced Ejection Fraction (HFrEF), defined as left ventricular ejection fraction (LVEF) less than or equal to (≤) 35% at Screening, including documented history of HFrEF (LVEF ≤ 35%) for at least 4 months prior to Screening * New York Heart Association Class II-IV * Cardiac index ≤ 2.5 liters per minute per square meter (L/min/m\^2) and pulmonary capillary wedge pressure ≥ 15 millimeters of mercury (mm Hg) at Day 1 * Body mass index 18.0 to 37.0 kilograms per square meter (kg/m\^2), inclusive, and body weight \< 150 kg at Screening and Day 1 Exclusion Criteria: * Hemodynamically unstable at Day 1 or in the opinion of the Investigator likely to progress to becoming hemodynamically unstable during the course of the study * Treated with carvedilol or at a dose higher than a total of 25 milligrams per day any time within 72 hours of Day 1 through the end of the in-clinic observation Post-dose Period. * Receiving any mechanical (respiratory or circulatory) or renal support therapy at Screening or Day 1 * Systolic Blood Pressure ≤ 90 millimeter of mercury (mm Hg) or ≥ 160 mm Hg, or Heart Rate \< 50 beats per minute (bpm) or \> 110 bpm, at Screening or Day 1 * Recently treated with inotropic, intravenous (IV) vasoactive or IV diuretic therapy, or expected to require such therapy with these drugs any time from Day 1 through the end of study conduct.
Locations (21)
- Tampa, Florida, United States
- Peoria, Illinois, United States
- Houston, Texas, United States
- Salt Lake City, Utah, United States
- Madison, Wisconsin, United States
- Bernau bei Berlin, Brandenburg, Germany
- Bad Nauheim, Germany
- Greifswald, Germany
- Nea Ionia, Athens, Greece
- Pylaia, Thessaloniki, Greece
- Larissa, Greece
- Gniezno, Poland
- Krakow, Poland
- Wroclaw, Poland
- Belgrade, Serbia
- Belgrade, Serbia
- Belgrade, Serbia
- Belgrade, Serbia
- Kamenitz, Serbia
- Kragujevac, Serbia
- Užice, Serbia