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NO DISPONIBLE

A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, ACTIVE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LCZ696 COMPARED TO ENALAPRIL ON MORBIDITY AND MORTALITY IN PATIENTS WITH CHRONIC HEART FAILURE AND REDUCED EJECTION FRACTION

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REPEC
Registry ID
PER-041-10
Enrollment
100
Registered
2010-08-03
Start date
2011-01-05
Completion date
Unknown
Last updated
2023-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Arm 1 (Experimental): LCZ696 single-blind active run-in period consisted of treatment with enalapril 10 mg bid, followed by LCZ696 100 mg bid, and then LCZ696 200 mg bid over a total duration of

Sponsors

NOVARTIS BIOSCIENSES PERU S.A.,
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients must give written informed consent before any assessment is performed. 2. Outpatients ≥ 18 years of age, male or female. 3. Patients with a diagnosis of CHF NYHA class II-IV and reduced ejection: • LVEF ≤ 40% at visit 1 (any local measurement, made within the past 6 months using echocardiography, MUGA, CT scanning, MRI or ventricular angiography is acceptable, provided no subsequent measurement above 40%) • BNP ≥150 pg/ml (NT-proBNP ≥600 pg/ml) at Visit 1 OR BNP ≥100 pg/mL (NT-proBNP ≥ 400 pg/ml) and a hospitalization for HF within the last 12 months 4. Patients must be on an ACEI or an ARB at a stable dose of at least enalapril 10 mg/d or equivalent for at least 4 weeks before Visit 1. 5. Patients must be treated with a β-blocker, unless contraindicated or not tolerated, at a stable dose for at least 4 weeks prior to Visit 1.

Exclusion criteria

Exclusion criteria: 1. Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer. 2. History of hypersensitivity or allergy to any of the study drugs, drugs of similar chemical classes, ACEIs, ARBs, or NEP inhibitors as well as known or suspected contraindications to the study drugs. 3. Previous history of intolerance to recommended target doses of ACEIs or ARBs 4. Known history of angioedema. 5. Requirement of treatment with both ACEIs and ARBs. 6. Current acute decompensated HF (exacerbation of chronic HF manifested by signs and symptoms that may require intravenous therapy). 7. Symptomatic hypotension and/or a SBP 5.2 mmol/L at Visit 1 (screening) or > 5.4 mmol/L at Visit 3 or Visit 5 (randomization) Other protocol-defined exclusion criteria apply.

Contacts

Public ContactAlexandra Lopez

NOVARTIS BIOSCIENCES PERU S.A.

alexandra.lopez@novartis.com4942788 anexo 145

Outcome results

None listed

Source: REPEC (via WHO ICTRP)