ClinicalTrials.Veeva

Menu

The ENCHANTMENT HIV Study

Mass General Brigham logo

Mass General Brigham

Status and phase

Completed
Phase 2

Conditions

Heart Failure With Preserved Ejection Fraction
HIV/AIDS

Treatments

Drug: Sacubitril-Valsartan 49-51Mg Oral Tablet
Drug: Placebo oral tablet

Study type

Interventional

Funder types

Other

Identifiers

NCT04153136
MGH2019P002355

Details and patient eligibility

About

Persons with HIV, even those well-treated, are at increased risk for heart disease when compared to the general population. Two hormones called aldosterone and brain natriuretic peptide (BNP), which have been shown to be abnormal in HIV, may be associated with inflammation as well as early changes in structure and function of the heart. This study is being conducted to evaluate whether therapies to block aldosterone and increase BNP levels may reduce the burden and progression of heart failure to improve cardiovascular health.

Full description

This is a 6-month study enrolling persons with HIV with no known history of heart disease. Participants will be screened for early signs of heart failure using cardiac ultrasound (cardiac transthoracic echocardiography or cardiac TTE). Those participants who have early changes in the structure and function of the heart and may be at future risk for heart failure will be enrolled into the study. Additional imaging of the heart will occur using cardiac magnetic resonance imaging (cardiac MRI). Following baseline studies, participants will either receive a medication called sacubitril/valsartan or placebo for 6 months. Sacubitril/valsartan in an FDA approved medication currently being used for heart failure with reduced ejection fraction in the general population, and we are evaluating whether this medication could be useful to reduce HIV-related heart failure with preserved ejection fraction. Sacubitril/valsartan is an oral medication taken twice daily that may block aldosterone hormone and increase natriuretic peptide hormone. Overall, this study aims to investigate the effect of sacubitril/valsartan on measures of heart disease related to inflammation, structure and function of the heart muscle in HIV using cardiac TTE and cardiac MRI imaging as well as blood markers of heart failure and inflammation.

Enrollment

39 patients

Sex

All

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Antiretroviral therapy use for >12 months

  2. HIV Viral Load <200 copies/mL

  3. Left Ventricular Ejection Fraction>50%

  4. Demonstration of one or more criteria for myocardial dysfunction on cardiac transthoracic echocardiogram, relevant to the progression of heart failure with preserved ejection fraction:

    • Left Atrial Volume Index > 28 mL/m2
    • Global Longitudinal Strain <18%
    • Left Ventricular Mass Index > 95g/m2 (female), 115 g/m2 (male)

Exclusion criteria

  1. Known history of congestive heart failure or valvular disease
  2. Recent cardiac event or stroke within 3 months
  3. Current medication use acting along the RAAS pathway (ACEi, ARB, MR blockade, direct renin inhibitor), potassium (K) supplementation or diuretic
  4. Angioedema to ACEi or ARB
  5. SBP<100 mmHg
  6. Medication suspected to have contraindication with active study drug
  7. Steroid use within last 3 months
  8. Uncontrolled diabetes requiring insulin and/or HbA1c > 7.5%
  9. Creatinine (Cr)>1.5 mg/dL and estimated GFR<60 mL/min/1.73m2
  10. K>5.5 mEq/L
  11. Hemoglobin <10.0 g/dL
  12. Known liver disease or ALT>3x upper limit normal
  13. Pregnant, actively seeking pregnancy or breastfeeding
  14. Estrogen, progestin derivative, or other sex steroid use within 3 months. Stable physiologic testosterone replacement (> 3 months) is acceptable
  15. Current bacterial or other infection
  16. Active substance abuse
  17. Known reaction to gadolinium

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

39 participants in 2 patient groups, including a placebo group

Sacubitril/Valsartan
Experimental group
Description:
Sacubitril/Valsartan 49-51mg twice daily along with lifestyle modification (counseling regarding diet and healthy activity) for 6 months
Treatment:
Drug: Sacubitril-Valsartan 49-51Mg Oral Tablet
Placebo
Placebo Comparator group
Description:
Placebo twice daily along with lifestyle modification (counseling regarding diet and healthy activity) for 6 months
Treatment:
Drug: Placebo oral tablet

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Suman Srinivasa, MD, MS

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems