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

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