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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Trial Officials
Novartis Pharmaceuticals
Study Director
Novartis Pharmaceuticals
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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