All compounds are either investigational or being studied for (a) new use(s). Efficacy and safety have not been established. There is no guarantee that they will become commercially available for the use(s) under investigation.
The purpose of this study is to generate effectiveness data of ARNI, in the Chinese HFrEF patients with implanted ICD or CRT-D. This will be a multicenter, interventional, open-label, and prospective single-arm study to evaluate the effect of ARNI on VAs in approximately 275 HFrEF patients receiving ICD or CRT-D in China.
Nov 11, 2020
Aug 31, 2022
18 Years - 80 Years (Adult, Older Adult)
initative ACE/ARB drug for 6 months in this study
initative ARNI drug for next 6 months in this study
Key Inclusion criteria:
Male or female patients ≥18 and ≤80 years of age
Implanted with an ICD or CRT-D within 2 weeks
NYHA functional class II - IV
LVEF ≤40% (measured by echocardiography)
Signed informed consent must be obtained prior to participation in the study.
Key Exclusion criteria
History of hypersensitivity to any of the study treatments or its excipients or to drugs of similar chemical classes.
Patients who received ARNI within 6 weeks prior to study enrollment
Participation in other clinical studies 3 months prior to participating study
Advanced cancer or other significant comorbidities with life expectancy of <1 year
Previous history of angioedema associated with ACEI/ARB treatment, hereditary or idiopathic angioedema
Patients with renal artery stenosis history
Current stage D HF patients requiring vasoactive drugs
Symptomatic hypotension < 100/60 mmHg at Visit 1 (screening) or Symptomatic hypotension < 90/60 mmHg in anti-hypertension drug treatment at Visit 1 (screening)
Serum potassium >5.4 mmol/L at Visit 1 (screening)
Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73m2 as measured at Visit 1 (screening)
Pregnant or nursing (lactating) women
Other exclusion depend on investigator's discretion
Other protocol- defined inclusion/exclusion criteria may apply