The trial was terminated early, on the recommendation of the Data Monitoring Committee, due to a sustained and highly significant reduction in the risk of the primary composite end point (CV death or HF hospitalisation) and in CV mortality in the sacubitril/valsartan group compared with the enalapril group.
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The neprilysin pathway in heart failure: a review and guide on the use of sacubitril/valsartan.
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