drugset / Trial / NCT01951625

Phase IIb Safety and Efficacy Study of Four Dose Regimens of BAY1021189 in Patients With Heart Failure With Reduced Ejection Fraction Suffering From Worsening Chronic Heart Failure (SOCRATES-REDUCED)

NCT01951625 ↗

Phase 2 Completed 456 enrolled Bayer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Objective of the study is to find the optimal dose of the once daily oral soluble guanylate cyclase stimulator (sGC) BAY1021189 for Phase III that can be given in addition to standard therapy for heart failure with reduced ejection fraction (HFrEF).

Timeline

Start
2013-11-29
Primary completion
2015-05-14
Completion
2015-06-09

Outcome

Missed primary endpoint

paper In primary analysis, change in log-transformed NT-proBNP levels from baseline to week 12 was not significantly different between the pooled vericiguat group PMID 26547357 ↗

paper vericiguat did not have a statistically significant effect on change in NT-proBNP level at 12 weeks PMID 26547357 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vericiguat Other / unclassified 1.25 mg Oral
Subject Vericiguat Other / unclassified 2.5 mg Oral
Subject Vericiguat Other / unclassified 5 mg Oral
Subject Vericiguat Other / unclassified 10 mg Oral

Indications