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There is limited long-term evidence specific to AAs with HFrEF on sacubitril/valsartan therapy. Plasma NT-proBNP levels are lower in AA individuals as compared to Caucasian individuals in general. However, the mechanism of action of sacubitril specifically targets the activity of BNP. Therefore, there is the potential that the mechanism of action of sacubitril/valsartan may be less effective in AAs.
To assess the efficacy and safety of sacubitril/valsartan in AA patients with HFrEF by comparing the outcomes of AA patients on ARNI therapy plus SOC (with or without hydralazine/isosorbide \[H-IDSN\]) to AA patients receiving ACEi/ARB therapy plus SOC (with or without H-ISDN).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Methodist Dallas Medical Center Pharmacy
Dallas, Texas, United States
Start Date
August 13, 2020
Primary Completion Date
August 1, 2024
Completion Date
August 1, 2024
Last Updated
March 27, 2024
352
ESTIMATED participants
sacubitril/valsartan
DRUG
Lead Sponsor
Methodist Health System
NCT07191730
NCT07484009
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