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Phase 4 N=302 Supportive Care

Description of Tolerability of LCZ696 (Sacubitril / Valsartan) in Heart Failure With Reduced Ejection Fraction (HFrEF) Treated in Real Life Setting

Hearth Failure With Reduced Ejection Fraction (HFrEF)

Enrolled (actual)
302
Serious AEs
15.6%
Results posted
Jun 2019
Primary outcome: Primary: Percentage of Participants on LCZ696 200 mg Bid at Month 6 — 64.6 Percentage of Participants

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
LCZ696 (sacubitril/valsartan) (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Novartis Pharmaceuticals
Primary completion
Jun 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants on LCZ696 200 mg Bid at Month 6
64.6
SECONDARY
Percentage of Participants on LCZ696 200 mg Bid at Month 12
62.3
SECONDARY
Percentage of Participants Requiring Down-titration From LCZ696 200 mg
11.92
SECONDARY
Percentage of Participants With Down-titration Changes From LCZ696 200 mg During 12 Months of Treatment
188; 44; 28
SECONDARY
Change From Baseline in the Six Minute Walk Test (6MWT) at Month 6 and Month 12
392.62; 11.99; 8.19
SECONDARY
Time to Each Up-titration to LCZ696 100 mg and LCZ696 200 mg
21.44; 27.37; 46.61
SECONDARY
Median Time to Reach LCZ696 200 mg
37.00
SECONDARY
Percentage of Participants on Guideline Recommended Dose of Beta-blockers and MRAs Over Time
298; 272; 261

Summary

The primary purpose of the study was to describe the tolerability of treatment with the optimal dose of LCZ696 (97 mg sacubitril / 103 mg valsartan bid), over six (6) months, in patients with heart failure with reduced ejection fraction (HFrEF) in Canada. The study was also to describe the overall tolerability, effectiveness and safety of LCZ696 for the management of HFrEF over 12 months of treatment, as well as describe the patterns of LCZ696 up and down dose titrations occurring during the management of patients with HFrEF.

Eligibility Criteria

Key Inclusion Criteria

  • Written informed consent must be obtained before any assessment is performed.
  • Age ≥ 18 years and ≤ 80 years.
  • Males or females.
  • Diagnosis of Heart Failure NYHA class II-III.
  • Diagnosis of Heart Failure with reduced Ejection Fraction (LVEF =< 40%) and NYHA class II or III.
  • Stable on any dose of ACEI or ARB prior to enrolment in the study
  • Stable on any dose of a beta-blocker prior to enrolment in the study.
  • Eligible for treatment with LCZ696 as per Canadian product monograph.
  • Treated as an outpatient.
  • Signed an informed consent agreeing to participate in the study.

Key Exclusion Criteria

  • Symptomatic hypotension and/or a SBP < 100 mmHg at baseline visit.
  • Estimated GFR < 30 mL/min/1.73m^2 as measured by the simplified Modification of Diet in Renal Disease (MDRD) formula at baseline visit.
  • Known history of angioedema related to previous ACEI or ARBs therapy, or history of hereditary or idiopathic angioedema.
  • Requirement of concomitant treatment with both ACEIs and ARBs.
  • Concurrent participation in other clinical trials or receiving other investigational drugs within 30 days of enrollment.
  • Hypersensitivity to the active substances, sacubitril or valsartan, or to any of the excipients.
  • Concomitant use of aliskiren-containing drugs in patients with diabetes mellitus (type 1 or type 2) or moderate to severe renal impairment (GFR <60ml/min/1.73m^2).
  • History of hypersensitivity to any of the study drugs or to drugs of similar chemical classes.
  • History of malignancy of any organ system (other than localized basal cell carcinoma of the skin), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.
  • Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test.
  • Women of childbearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using effective methods of contraception during dosing of study treatment. Effective contraception methods are described in the protocol.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02690974). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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