"Conclusions and Relevance Among patients with worsening chronic HF and reduced LVEF, compared with placebo, vericiguat did not have a statistically significant effect on change in NT-proBNP level at 12 weeks but was well-tolerated. Further clinical trials of vericiguat based on the dose-response relationship in this study are needed to determine the potential role of this drug for patients with worsening chronic HF.
Trial Registration clinicaltrials.gov Identifier: NCT01951625"
http://jama.jamanetwork.com/article.aspx?articleid=2469195
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