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Search / Trial NCT02874794

Study of Effects of Sacubitril/Valsartan vs. Enalapril on Aortic Stiffness in Patients With Mild to Moderate HF With Reduced Ejection Fraction

Launched by NOVARTIS PHARMACEUTICALS · Aug 17, 2016

Trial Information

Current as of June 07, 2025

Completed

Keywords

Heart Failure Reduced Ejection Fraction Central Aortic Stiffness Vascular Echocardiogram Aortic Stiffness

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • * History of HTN and one of the following at BOTH screening and pre-randomization:
  • 1. SBP \>105 mm Hg on antihypertensive medication.
  • 2. SBP \>/= 140 mm Hg and NOT on antihypertensive medication.
  • NYHA class I-III heart failure and with reduced ejection fraction \</= 40%, as determined by any local measurement made within the past 12 months using echocardiography, MUGA, CT scanning, MRI, ventricular angiography or single-photon emission computed tomography (SPECT), provided no subsequent measurement above 40%. Patients who have had an intervening medical event (e.g. myocardial infarction) or procedure (e.g. revascularization, cardiac resynchronization), must have a reassessment of EF ≥ 3 months following the event to ensure that eligibility criteria are still met.
  • On stable doses of treatment with guideline-directed therapy, other than ACEis and ARBs prior to randomization.
  • 1. If the patient is currently taking an ACEi, a 36-hour washout is required prior to randomization (Visit 2).
  • 2. If the patient is currently taking an ARB, they must discontinue the ARB before initiation of study treatment however washout is not required.
  • On an optimal medical regiment of diuretics and background medications to effectively treat co-morbidities such as HTN, DM, and coronary artery disease.
  • Key Exclusion Criteria:
  • History of hypersensitivity to any of the study drigs, including history of hypersensitivity to drugs of similar chemical classes, or allergy to ACEis, ARBs, or NEP inhibitors as well as known or suspected contraindications to the study drugs.
  • Previous history of intolerance to sacubitril and valsartan, ACEi or ARB standard of care doses despite appropriate and gradual up-titration.
  • History of angioedema, drug-related or otherwise.
  • Requirement of treatment with both ACE inhibitor and ARB.
  • Current or prior treatment with sacubitril and valsartan.

About Novartis Pharmaceuticals

Novartis Pharmaceuticals is a global healthcare company dedicated to reimagining medicine to improve and extend people's lives. With a strong focus on innovation, Novartis engages in the research, development, and commercialization of a broad range of therapies across various therapeutic areas, including oncology, cardiology, dermatology, and neuroscience. The company is committed to advancing scientific knowledge and patient care through clinical trials that prioritize safety and efficacy. Novartis leverages cutting-edge technology and collaborative partnerships to address unmet medical needs and deliver transformative treatments that enhance patient outcomes worldwide.

Locations

Northridge, California, United States

Greenville, North Carolina, United States

Birmingham, Alabama, United States

Newport Beach, California, United States

Macon, Georgia, United States

Baltimore, Maryland, United States

Mountain Lakes, New Jersey, United States

Las Vegas, Nevada, United States

Beverly Hills, California, United States

Augusta, Georgia, United States

Buffalo, New York, United States

Jupiter, Florida, United States

Overland Park, Kansas, United States

Omaha, Nebraska, United States

Lake Success, New York, United States

Jackson, Tennessee, United States

Newark, Delaware, United States

Huntington Beach, California, United States

Aventura, Florida, United States

Slidell, Louisiana, United States

Greenwich, Connecticut, United States

Trumbull, Connecticut, United States

Hialeah, Florida, United States

Spokane, Washington, United States

Daytona Beach, Florida, United States

Athens, Georgia, United States

Lincoln, Nebraska, United States

Coeur D'alene, Idaho, United States

Blue Ridge, Georgia, United States

Stamford, Connecticut, United States

Jacksonville, Florida, United States

Richmond, Virginia, United States

Miami, Florida, United States

Little Rock, Arkansas, United States

Bradenton, Florida, United States

Doral, Florida, United States

Sherman, Texas, United States

Santa Ana, California, United States

Owensboro, Kentucky, United States

Baton Rouge, Louisiana, United States

Minden, Louisiana, United States

Mckinney, Texas, United States

Tomball, Texas, United States

Webster, Texas, United States

Van Nuys, California, United States

Gurnee, Illinois, United States

Coral Gables, Florida, United States

Naples, Florida, United States

Owosso, Michigan, United States

Richland, Washington, United States

Amarillo, Texas, United States

Atlantis, Florida, United States

Yardley, Pennsylvania, United States

Houston, Texas, United States

Rosedale, New York, United States

Norwalk, Connecticut, United States

Fort Lauderdale, Florida, United States

Inverness, Florida, United States

Saint Augustine, Florida, United States

Eatonton, Georgia, United States

Fairview Heights, Illinois, United States

Eunice, Louisiana, United States

Monroe, Louisiana, United States

Alpena, Michigan, United States

Saginaw, Michigan, United States

Hillsborough, New Jersey, United States

Linden, New Jersey, United States

Manalapan, New Jersey, United States

Bronx, New York, United States

Charlotte, North Carolina, United States

Lenoir, North Carolina, United States

Manitowoc, Wisconsin, United States

Patients applied

0 patients applied

Trial Officials

Novartis Pharmaceuticals

Study Director

Novartis Pharmaceuticals

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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