Study ID | Study design | Country | Total participants | sGC stimulator | HF type/NYHA class | Primary outcome | |||
---|---|---|---|---|---|---|---|---|---|
Drug | Dose | Times of administration | TTT duration | ||||||
Armstrong et al. 2020 (VITALITY-HFpEF) [8] | Phase IIb multicenter, double-blinded RCT | 21 countries | 789 | Vericiguat | 10 or 15 mg | Once daily | 24 weeks | HFpEF/NYHA II & III | Kansas City Cardiomyopathy Questionnaire Physical Limitation Score (KCCQ PLS) |
Armstrong et al. 2020 (VICTORIA) [2] | Phase III multicenter, double-blinded RCT | 42 countries | 5050 | Vericiguat | 10 mg | Once daily | N/A | HFrEF/NYHA II–IV | The composite of death from cardiovascular causes or first hospitalization for heart failure |
Bonderman et al. 2013 (LEPHT) [10] | Phase IIb multicenter, double-blinded RCT | 18 countries | 201 | Riociguat | 0.5, 1, or 2 mg | Three times daily | 16 weeks | HFrEF/NYHA II–IV | mPAP change |
Bonderman et al. 2014 (DILATE-1) [7] | Phase II multicenter, double-blinded RCT | Austria, the Czech Republic, and Germany | 39 | Riociguat | 0.5, 1, or 2 mg | Once daily | N/A | HFpEF | mPAP change |
Dachs et al. 2022 (haemoDYNAMIC) [9] | Phase IIb multicenter, double-blinded RCT | Austria and Germany | 114 | Riociguat | 0.5 mg (up-)titrated to 1.0 of 1.5 mg | Three times daily | 30 weeks | HFpEF | CO change |
Gheorghiade et al. 2015 (SOCRATES-Reduced) [9] | Multicenter, double-blinded RCT | Europe, North America, and Asia | 456 | Vericiguat | 1.25, 2.5, 5, or 10 mg | Once daily | 12 weeks | HFrEF/NYHA II–IV | NT-proBNP change |
Pieske et al. 2017 (SOCRATES-PRESERVED) [12] | Multicenter, double-blinded RCT | United States and Germany | 477 | Vericiguat | 1.25, 2.5, 5, or 10 mg | Once daily | 12 weeks | HFpEF/NYHA II–IV | NT-proBNP change |
Udelson et al. 2020 (CAPACITY HFpEF) [11] | Phase II multicenter, double-blinded RCT | United States and Canada | 181 | Praliciguat | 40 mg | N/A | 12 weeks | HFpEF/NYHA II–IV | Peak VO2 change |