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Completed Phase 2 Interventional Results available

Safety and Tolerability of Initiating LCZ696 in Heart Failure Patients

ClinicalTrials.gov ID: NCT01922089

Public ClinicalTrials.gov record NCT01922089. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 2:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Parallel Group Study to Assess the Safety and Tolerability of Initiating LCZ696 in Heart Failure Patients Comparing Two Titration Regimens

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety and tolerability of initiating LCZ696 in heart failure patients with reduced ejection fraction (HF-rEF) using conservative (reaching target dose over 6 weeks) and condensed (reaching target dose over 3 weeks) up-titration regimens.

Study identification

NCT ID
NCT01922089
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
498 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2013 (Type not available)
Primary completion
Aug 2014 (Actual)
Completion
Aug 2014 (Actual)
Last update posted
Oct 15, 2015

2013 – 2014

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Novartis Investigative Site Anchorage Alaska 99508 —
Novartis Investigative Site Gilbert Arizona 85297 —
Novartis Investigative Site Tucson Arizona 85710 —
Novartis Investigative Site Anaheim California 92801 —
Novartis Investigative Site Torrance California 90502 —
Novartis Investigative Site Atlantis Florida 33462 —
Novartis Investigative Site Chiefland Florida 32626 —
Novartis Investigative Site Aurora Illinois 60504 —
Novartis Investigative Site Peoria Illinois 61602 —
Novartis Investigative Site Evansville Indiana 47714 —
Novartis Investigative Site Slidell Louisiana 70458 —
Novartis Investigative Site Minneapolis Minnesota 55417 —
Novartis Investigative Site St Louis Missouri 63110 —
Novartis Investigative Site Buffalo New York 14215 —
Novartis Investigative Site Laurelton New York 11422 —
Novartis Investigative Site Marion Ohio 43302 —
Novartis Investigative Site Oak Ridge Tennessee 37830 —
Novartis Investigative Site Dallas Texas 75231 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site Houston Texas 77094 —
Novartis Investigative Site Livingston Texas 77351 —
Novartis Investigative Site Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 83 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01922089, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 15, 2015 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01922089 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →