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Efficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With CCC (PARACHUTE-HF)

Primary Purpose

Chagas Disease, Heart Failure

Status
Active
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Sacubitril/valsartan
Enalapril
Sponsored by
Novartis Pharmaceuticals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chagas Disease focused on measuring Chagas' disease, heart failure, angiotensin receptor-neprilysin inhibitor, ARNI, ARB, ACEI, sacubitril/valsartan, enalapril

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Key Inclusion Criteria:

  • Male or female ≥ 18 years of age
  • Diagnosis of NYHA Class II-IV HFrEF established by:

    1. LVEF ≤ 40% within 12 months prior to Visit 1 made by any local measurement using echocardiography, multiple gated acquisition scan (MUGA), computerized tomography (CT) scanning, magnetic resonance imaging (MRI), or ventricular angiography, provided no subsequent measurement above 40% AND
    2. NT-proBNP ≥ 600 pg/mL (or BNP ≥ 150 pg/mL) at Visit 1 OR
    3. NT-proBNP ≥ 400 pg/mL (or BNP ≥ 100 pg/mL) at Visit 1 and a hospitalization for HF within the last 12 months
  • Chagas' disease diagnosis confirmed by at least two different serological tests for anti-Trypanosoma cruzi based on different principles or with different antigenic preparations, such as: enzyme-linked immunosorbent assay [ELISA], indirect immunofluorescence [IFI], indirect hemagglutination [IHA], western blot (WB), chemiluminescent immunoassay (CLIA). If documented history is not available, the tests may be performed during the screening

Key Exclusion Criteria:

  • Patients with history of suspected or proven angioedema or unable to tolerate ACEIs, ARBs or ARNI (e.g., due to cough, hypotension, renal dysfunction, hyperkalemia)
  • Use of sacubitril/valsartan in the past 3 months
  • Patients requiring continuous intravenous inotropic therapy or with indication of advanced support intervention for HF:

    1. already on list for a heart transplantation
    2. with current indication of left ventricular assist device, or cardiac resynchronization therapy (CRT)
  • Systemic systolic blood pressure lower than 95 mmHg or symptomatic hypotension
  • Serum potassium > 5.2 mmol/L
  • Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2 of body surface area
  • Severe gastrointestinal form of chronic Chagas' disease (demonstrated megaesophagus and/or important megacolon, e.g.: with compromised oral intake or surgical indication).
  • Clinical conditions or systemic diseases limiting proper patient participation
  • Pregnant or nursing women or women of child-bearing potential unless they are using highly effective methods of contraception
  • Presence of other cardiac conditions:

    1. Previous cardiac surgery
    2. Heart failure where, in the Investigator's judgement, there is a possible alternative primary etiology e.g., due to coronary artery disease, valve disease, congenital heart disease or other causes.
    3. Untreated arrhythmia or serious conduction disease e.g., bradyarrhythmias, atrial fibrillation with rapid ventricular response, second or third degree atrioventricular block, etc.
    4. Primary uncorrected valvar pathology like moderate to severe aortic stenosis, mitral stenosis and primary mitral regurgitation
    5. Planned organ transplantation (or in listing for transplantation), planned cardiac or other major surgery (including ventricular assist device implantation)
  • History of malignancy of any organ system within the past 5 years.
  • Current confirmed COVID19 infection
  • Past COVID19 infection with persistent symptom burden suspected due to COVID19 (persistent symptoms may include, but are not limited to, continued cough, breathing difficulty, muscle/joint aches, and gastrointestinal symptoms from the time of COVID19 infection onward)

Sites / Locations

  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site
  • Novartis Investigative Site

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sacubitril/valsartan

Enalapril

Arm Description

Sacubitril/valsartan 200 mg b.i.d. Following randomization, patients will receive sacubitril/valsartan in titrated doses from level 1 up to level 3 (50, 100 and 200 mg twice daily). Participants taking ACEIs who are randomized to sacubitril/valsartan will do a 36-hour ACEI washout before they start taking the study drug Sacubitril/valsartan in dose levels of 50 mg, 100 mg, and 200 mg are equivalent to sacubitril/valsartan 24/26 mg, 49/51 mg and 97/103 mg, respectively

Enalapril 10 mg b.i.d. Following randomization, patients will receive the enalapril in titrated doses from level 1 up to level 3 (2.5, 5 and 10 mg twice daily).

Outcomes

Primary Outcome Measures

Hierarchical composite endpoint composed of time to CV death, time to first HF hospitalization, relative change in NT-proBNP from baseline to Week 12
The primary efficacy endpoint will be analyzed using the win ratio approach comparing every participant in the sacubitril/valsartan arm to every participant in the enalapril arm to determine a winner. The estimated win ratio (the total number of winners in the sacubitril/valsartan arm divided by the total number of winners in the enalapril arm) will be provided. A winner in the pair-wise comparison has a delayed time to the occurrence of CV death; if time to the occurrence of CV death is censored, a winner has a delayed time to the occurrence of first HF hospitalization event; if the times to both CV events are censored, a winner has a more favorable (less increase or more decrease) change in NT-proBNP between Baseline and Week 12.

Secondary Outcome Measures

Time to the first occurrence of a composite of CV events
Time from randomization to the first occurrence of HF hospitalization or CV death
Time to all-cause mortality
The time to all-cause mortality will be determined.
Time to sudden death or resuscitated sudden cardiac arrest
The time to sudden death or resuscitated sudden cardiac arrest will be determined.
Number of visits to an ER due to HF (where intravenous therapy is required)
The rate of visits to an emergency room (ER) due to HF (where intravenous therapy is required) will be determined.
Number of days alive out of the hospital
The number of days alive out of the hospital will be determined.
Number of ventricular fibrillation or sustained ventricular tachycardia
The number of ventricular fibrillation or sustained ventricular tachycardia needing specific pharmacological, electrical or other treatment will be determined.
Number of anti-tachycardia pacing or shock therapies
This will be determined in a subset on a subset of participants who have an ICD or CRT-D at Randomization.

Full Information

First Posted
July 10, 2019
Last Updated
October 19, 2023
Sponsor
Novartis Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT04023227
Brief Title
Efficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With CCC
Acronym
PARACHUTE-HF
Official Title
A Multicenter, Prospective, Randomized, Open-label, Blinded-endpoint, Phase 4 Study to Evaluate the Efficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With Chronic Chagas' Cardiomyopathy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 10, 2019 (Actual)
Primary Completion Date
September 16, 2024 (Anticipated)
Study Completion Date
September 16, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Novartis Pharmaceuticals

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effect of sacubitril/valsartan 200 mg BID compared with enalapril 10 mg BID, in addition to conventional heart failure (HF) treatment, in improving a hierarchical composite of cardiovascular (CV) events (i.e. CV death or the occurrence of first HF hospitalization) and causing a greater reduction in n terminal prohormone of brain natriuretic peptide (NT-proBNP, at Week 12 from Baseline) in participants with HF with reduced ejection fraction (HFrEF) caused by CCC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chagas Disease, Heart Failure
Keywords
Chagas' disease, heart failure, angiotensin receptor-neprilysin inhibitor, ARNI, ARB, ACEI, sacubitril/valsartan, enalapril

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
This is a Phase 4, multinational, multicenter, parallel-group, prospective, randomized, open-label, blinded-endpoint adjudication, active-controlled study to demonstrate superiority of sacubitril/valsartan over enalapril in improving a composite of CV events (CV death or first HF hospitalization), or in causing greater reduction or lesser increase in NT-proBNP levels at Week 12 in participants with HFrEF caused by CCC.
Masking
Outcomes Assessor
Masking Description
Endpoint Adjudication Committee will be blinded to treatment allocation.
Allocation
Randomized
Enrollment
920 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sacubitril/valsartan
Arm Type
Experimental
Arm Description
Sacubitril/valsartan 200 mg b.i.d. Following randomization, patients will receive sacubitril/valsartan in titrated doses from level 1 up to level 3 (50, 100 and 200 mg twice daily). Participants taking ACEIs who are randomized to sacubitril/valsartan will do a 36-hour ACEI washout before they start taking the study drug Sacubitril/valsartan in dose levels of 50 mg, 100 mg, and 200 mg are equivalent to sacubitril/valsartan 24/26 mg, 49/51 mg and 97/103 mg, respectively
Arm Title
Enalapril
Arm Type
Active Comparator
Arm Description
Enalapril 10 mg b.i.d. Following randomization, patients will receive the enalapril in titrated doses from level 1 up to level 3 (2.5, 5 and 10 mg twice daily).
Intervention Type
Drug
Intervention Name(s)
Sacubitril/valsartan
Other Intervention Name(s)
LCZ696; Entresto; Vymada
Intervention Description
50 (24/26) mg, 100 (49/51) mg and 200 (97/103) mg will be available for dose adjustments.
Intervention Type
Drug
Intervention Name(s)
Enalapril
Other Intervention Name(s)
Renitec
Intervention Description
5 mg and 10 mg will be available for dose adjustments.
Primary Outcome Measure Information:
Title
Hierarchical composite endpoint composed of time to CV death, time to first HF hospitalization, relative change in NT-proBNP from baseline to Week 12
Description
The primary efficacy endpoint will be analyzed using the win ratio approach comparing every participant in the sacubitril/valsartan arm to every participant in the enalapril arm to determine a winner. The estimated win ratio (the total number of winners in the sacubitril/valsartan arm divided by the total number of winners in the enalapril arm) will be provided. A winner in the pair-wise comparison has a delayed time to the occurrence of CV death; if time to the occurrence of CV death is censored, a winner has a delayed time to the occurrence of first HF hospitalization event; if the times to both CV events are censored, a winner has a more favorable (less increase or more decrease) change in NT-proBNP between Baseline and Week 12.
Time Frame
Total follow up time up to approximately 36 months
Secondary Outcome Measure Information:
Title
Time to the first occurrence of a composite of CV events
Description
Time from randomization to the first occurrence of HF hospitalization or CV death
Time Frame
From the date of randomization to the first occurrence (total follow up time up to approximately 36 months)
Title
Time to all-cause mortality
Description
The time to all-cause mortality will be determined.
Time Frame
From date of randomization until the date of death from any cause assessed up to the end of the study, which is estimated to be up to approximately 36 months
Title
Time to sudden death or resuscitated sudden cardiac arrest
Description
The time to sudden death or resuscitated sudden cardiac arrest will be determined.
Time Frame
From date of randomization until the date of the sudden death or resuscitated sudden cardiac arrest assessed up to the end of the study, which is estimated to be up to approximately 36 months
Title
Number of visits to an ER due to HF (where intravenous therapy is required)
Description
The rate of visits to an emergency room (ER) due to HF (where intravenous therapy is required) will be determined.
Time Frame
From the date of randomization up to End of Study (EOS) assessment. Total follow up time up to approximately 36 months.
Title
Number of days alive out of the hospital
Description
The number of days alive out of the hospital will be determined.
Time Frame
From the date of randomization up to End of Study (EOS) assessment. Total follow up time up to approximately 36 months.
Title
Number of ventricular fibrillation or sustained ventricular tachycardia
Description
The number of ventricular fibrillation or sustained ventricular tachycardia needing specific pharmacological, electrical or other treatment will be determined.
Time Frame
From the date of randomization up to End of Study (EOS) assessment. Total follow up time up to approximately 36 months.
Title
Number of anti-tachycardia pacing or shock therapies
Description
This will be determined in a subset on a subset of participants who have an ICD or CRT-D at Randomization.
Time Frame
From the date of randomization up to End of Study (EOS) assessment. Total follow up time up to approximately 36 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: Male or female ≥ 18 years of age Diagnosis of NYHA Class II-IV HFrEF established by: LVEF ≤ 40% within 12 months prior to Visit 1 made by any local measurement using echocardiography, multiple gated acquisition scan (MUGA), computerized tomography (CT) scanning, magnetic resonance imaging (MRI), or ventricular angiography, provided no subsequent measurement above 40% AND NT-proBNP ≥ 600 pg/mL (or BNP ≥ 150 pg/mL) at Visit 1 OR NT-proBNP ≥ 400 pg/mL (or BNP ≥ 100 pg/mL) at Visit 1 and a hospitalization for HF within the last 12 months Chagas' disease diagnosis confirmed by at least two different serological tests for anti-Trypanosoma cruzi based on different principles or with different antigenic preparations, such as: enzyme-linked immunosorbent assay [ELISA], indirect immunofluorescence [IFI], indirect hemagglutination [IHA], western blot (WB), chemiluminescent immunoassay (CLIA). If documented history is not available, the tests may be performed during the screening Key Exclusion Criteria: Patients with history of suspected or proven angioedema or unable to tolerate ACEIs, ARBs or ARNI (e.g., due to cough, hypotension, renal dysfunction, hyperkalemia) Use of sacubitril/valsartan in the past 3 months Patients requiring continuous intravenous inotropic therapy or with indication of advanced support intervention for HF: already on list for a heart transplantation with current indication of left ventricular assist device, or cardiac resynchronization therapy (CRT) Systemic systolic blood pressure lower than 95 mmHg or symptomatic hypotension Serum potassium > 5.2 mmol/L Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2 of body surface area Severe gastrointestinal form of chronic Chagas' disease (demonstrated megaesophagus and/or important megacolon, e.g.: with compromised oral intake or surgical indication). Clinical conditions or systemic diseases limiting proper patient participation Pregnant or nursing women or women of child-bearing potential unless they are using highly effective methods of contraception Presence of other cardiac conditions: Previous cardiac surgery Heart failure where, in the Investigator's judgement, there is a possible alternative primary etiology e.g., due to coronary artery disease, valve disease, congenital heart disease or other causes. Untreated arrhythmia or serious conduction disease e.g., bradyarrhythmias, atrial fibrillation with rapid ventricular response, second or third degree atrioventricular block, etc. Primary uncorrected valvar pathology like moderate to severe aortic stenosis, mitral stenosis and primary mitral regurgitation Planned organ transplantation (or in listing for transplantation), planned cardiac or other major surgery (including ventricular assist device implantation) History of malignancy of any organ system within the past 5 years. Current confirmed COVID19 infection Past COVID19 infection with persistent symptom burden suspected due to COVID19 (persistent symptoms may include, but are not limited to, continued cough, breathing difficulty, muscle/joint aches, and gastrointestinal symptoms from the time of COVID19 infection onward)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Novartis Pharmaceuticals
Organizational Affiliation
Novartis Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Novartis Investigative Site
City
Caba
State/Province
Buenos Aires
ZIP/Postal Code
C1221ADC
Country
Argentina
Facility Name
Novartis Investigative Site
City
Caba
State/Province
Buenos Aires
ZIP/Postal Code
C1425BEI
Country
Argentina
Facility Name
Novartis Investigative Site
City
Ramos Mejia
State/Province
Buenos Aires
ZIP/Postal Code
B1704ETD
Country
Argentina
Facility Name
Novartis Investigative Site
City
San Martin
State/Province
Buenos Aires
ZIP/Postal Code
1604
Country
Argentina
Facility Name
Novartis Investigative Site
City
Temperley
State/Province
Buenos Aires
ZIP/Postal Code
1834
Country
Argentina
Facility Name
Novartis Investigative Site
City
Villa Maria
State/Province
Cordoba
ZIP/Postal Code
X5900JKA
Country
Argentina
Facility Name
Novartis Investigative Site
City
Ciudad de Salta
State/Province
Provincia De Salta
ZIP/Postal Code
A4406BPF
Country
Argentina
Facility Name
Novartis Investigative Site
City
Tucuman
State/Province
San Miguel De Tucuman
ZIP/Postal Code
T4000ICL
Country
Argentina
Facility Name
Novartis Investigative Site
City
Rosario
State/Province
Santa Fe
ZIP/Postal Code
2000
Country
Argentina
Facility Name
Novartis Investigative Site
City
Rosario
State/Province
Santa Fe
ZIP/Postal Code
S2000DIF
Country
Argentina
Facility Name
Novartis Investigative Site
City
San Miguel de Tucuman
State/Province
Tucuman
ZIP/Postal Code
T4000IFL
Country
Argentina
Facility Name
Novartis Investigative Site
City
San Miguel de Tucuman
State/Province
Tucuman
ZIP/Postal Code
T4000JCU
Country
Argentina
Facility Name
Novartis Investigative Site
City
Buenos Aires
ZIP/Postal Code
C1155 AHD
Country
Argentina
Facility Name
Novartis Investigative Site
City
Buenos Aires
ZIP/Postal Code
C1425AGP
Country
Argentina
Facility Name
Novartis Investigative Site
City
Cordoba
ZIP/Postal Code
X5003DCE
Country
Argentina
Facility Name
Novartis Investigative Site
City
Cordoba
ZIP/Postal Code
X5004BAL
Country
Argentina
Facility Name
Novartis Investigative Site
City
Cordoba
ZIP/Postal Code
X5006CBI
Country
Argentina
Facility Name
Novartis Investigative Site
City
Cordoba
ZIP/Postal Code
X5016KET
Country
Argentina
Facility Name
Novartis Investigative Site
City
Corrientes
ZIP/Postal Code
W3400
Country
Argentina
Facility Name
Novartis Investigative Site
City
Formosa
ZIP/Postal Code
P3600
Country
Argentina
Facility Name
Novartis Investigative Site
City
Formosa
ZIP/Postal Code
P3634XAR
Country
Argentina
Facility Name
Novartis Investigative Site
City
Mendoza
ZIP/Postal Code
M5500CHC
Country
Argentina
Facility Name
Novartis Investigative Site
City
Santa Fe
ZIP/Postal Code
S3000EOZ
Country
Argentina
Facility Name
Novartis Investigative Site
City
Santa Fe
ZIP/Postal Code
S3000FWO
Country
Argentina
Facility Name
Novartis Investigative Site
City
Santiago del Estero
ZIP/Postal Code
G4200AQK
Country
Argentina
Facility Name
Novartis Investigative Site
City
Salvador
State/Province
BA
ZIP/Postal Code
40050-410
Country
Brazil
Facility Name
Novartis Investigative Site
City
Salvador
State/Province
BA
ZIP/Postal Code
40110060
Country
Brazil
Facility Name
Novartis Investigative Site
City
Salvador
State/Province
BA
ZIP/Postal Code
40323-010
Country
Brazil
Facility Name
Novartis Investigative Site
City
Salvador
State/Province
BA
ZIP/Postal Code
41253-190
Country
Brazil
Facility Name
Novartis Investigative Site
City
Fortaleza
State/Province
CE
ZIP/Postal Code
60430 370
Country
Brazil
Facility Name
Novartis Investigative Site
City
Brasila
State/Province
DF
ZIP/Postal Code
70673623
Country
Brazil
Facility Name
Novartis Investigative Site
City
Brasilia
State/Province
DF
ZIP/Postal Code
70390-903
Country
Brazil
Facility Name
Novartis Investigative Site
City
Brasilia
State/Province
Distrito Federal
ZIP/Postal Code
70710-100
Country
Brazil
Facility Name
Novartis Investigative Site
City
Goiania
State/Province
Goias
ZIP/Postal Code
74223-060
Country
Brazil
Facility Name
Novartis Investigative Site
City
Goiania
State/Province
GO
ZIP/Postal Code
74223-130
Country
Brazil
Facility Name
Novartis Investigative Site
City
Goiania
State/Province
GO
ZIP/Postal Code
74605-020
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Luis
State/Province
MA
ZIP/Postal Code
65020-070
Country
Brazil
Facility Name
Novartis Investigative Site
City
Belo Horizonte
State/Province
MG
ZIP/Postal Code
30130-100
Country
Brazil
Facility Name
Novartis Investigative Site
City
Belo Horizonte
State/Province
MG
ZIP/Postal Code
30140 062
Country
Brazil
Facility Name
Novartis Investigative Site
City
Belo Horizonte
State/Province
MG
ZIP/Postal Code
30150-221
Country
Brazil
Facility Name
Novartis Investigative Site
City
Uberaba
State/Province
MG
ZIP/Postal Code
38025-440
Country
Brazil
Facility Name
Novartis Investigative Site
City
Uberlândia
State/Province
MG
ZIP/Postal Code
38400-328
Country
Brazil
Facility Name
Novartis Investigative Site
City
Belo Horizonte
State/Province
Minas Gerais
ZIP/Postal Code
30130-100
Country
Brazil
Facility Name
Novartis Investigative Site
City
Montes Claros
State/Province
Minas Gerais
ZIP/Postal Code
39401-001
Country
Brazil
Facility Name
Novartis Investigative Site
City
Passos
State/Province
Minas Gerais
ZIP/Postal Code
37904-020
Country
Brazil
Facility Name
Novartis Investigative Site
City
Uberlandia
State/Province
Minas Gerais
ZIP/Postal Code
38400 500
Country
Brazil
Facility Name
Novartis Investigative Site
City
Belem
State/Province
PA
ZIP/Postal Code
66087-660
Country
Brazil
Facility Name
Novartis Investigative Site
City
Recife
State/Province
PE
ZIP/Postal Code
50100-060
Country
Brazil
Facility Name
Novartis Investigative Site
City
Teresina
State/Province
Piaui
ZIP/Postal Code
64001-380
Country
Brazil
Facility Name
Novartis Investigative Site
City
Londrina
State/Province
PR
ZIP/Postal Code
86038-440
Country
Brazil
Facility Name
Novartis Investigative Site
City
Natal
State/Province
Rio Grande Do Norte
ZIP/Postal Code
59020-035
Country
Brazil
Facility Name
Novartis Investigative Site
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
20551-030
Country
Brazil
Facility Name
Novartis Investigative Site
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
22240-006
Country
Brazil
Facility Name
Novartis Investigative Site
City
Botucatu
State/Province
Sao Paulo
ZIP/Postal Code
3880-1001
Country
Brazil
Facility Name
Novartis Investigative Site
City
Braganca Paulista
State/Province
Sao Paulo
ZIP/Postal Code
13183-091
Country
Brazil
Facility Name
Novartis Investigative Site
City
Ribeirao Preto
State/Province
Sao Paulo
ZIP/Postal Code
14010-190
Country
Brazil
Facility Name
Novartis Investigative Site
City
Santo Andre
State/Province
Sao Paulo
ZIP/Postal Code
09080-001
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Jose do Rio Preto
State/Province
Sao Paulo
ZIP/Postal Code
15015-210
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Jose do Rio Preto
State/Province
Sao Paulo
ZIP/Postal Code
15015-750
Country
Brazil
Facility Name
Novartis Investigative Site
City
Campinas
State/Province
SP
ZIP/Postal Code
13020-431
Country
Brazil
Facility Name
Novartis Investigative Site
City
Campinas
State/Province
SP
ZIP/Postal Code
13060 080
Country
Brazil
Facility Name
Novartis Investigative Site
City
Campinas
State/Province
SP
ZIP/Postal Code
13060-904
Country
Brazil
Facility Name
Novartis Investigative Site
City
Indaiatuba
State/Province
SP
ZIP/Postal Code
13330-570
Country
Brazil
Facility Name
Novartis Investigative Site
City
Marilia
State/Province
SP
ZIP/Postal Code
17515-000
Country
Brazil
Facility Name
Novartis Investigative Site
City
Ribeirao Preto
State/Province
SP
ZIP/Postal Code
14048-900
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Jose do Rio Preto
State/Province
SP
ZIP/Postal Code
15090-000
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
04012 909
Country
Brazil
Facility Name
Novartis Investigative Site
City
São Paulo
State/Province
SP
ZIP/Postal Code
05403-000
Country
Brazil
Facility Name
Novartis Investigative Site
City
Tatuí
State/Province
SP
ZIP/Postal Code
18270-170
Country
Brazil
Facility Name
Novartis Investigative Site
City
Votuporanga
State/Province
SP
ZIP/Postal Code
15500 003
Country
Brazil
Facility Name
Novartis Investigative Site
City
Ijui
ZIP/Postal Code
98700-000
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Paulo
ZIP/Postal Code
01223-001
Country
Brazil
Facility Name
Novartis Investigative Site
City
Sao Paulo
ZIP/Postal Code
05403-000
Country
Brazil
Facility Name
Novartis Investigative Site
City
Bogota
State/Province
Cundinamarca
ZIP/Postal Code
110121
Country
Colombia
Facility Name
Novartis Investigative Site
City
Santa Marta
State/Province
Magdalena
ZIP/Postal Code
30360
Country
Colombia
Facility Name
Novartis Investigative Site
City
San Gil
State/Province
Santander
ZIP/Postal Code
684031
Country
Colombia
Facility Name
Novartis Investigative Site
City
Bogota DC
ZIP/Postal Code
110111
Country
Colombia
Facility Name
Novartis Investigative Site
City
Florida Blanca
ZIP/Postal Code
681001
Country
Colombia
Facility Name
Novartis Investigative Site
City
Floridablanca
ZIP/Postal Code
681004
Country
Colombia
Facility Name
Novartis Investigative Site
City
Ciudad de Mexico
State/Province
Cdmx
ZIP/Postal Code
14080
Country
Mexico
Facility Name
Novartis Investigative Site
City
Merida
State/Province
Yucatan
ZIP/Postal Code
97000
Country
Mexico
Facility Name
Novartis Investigative Site
City
Oaxaca
ZIP/Postal Code
68000
Country
Mexico
Facility Name
Novartis Investigative Site
City
Xalapa
ZIP/Postal Code
91193
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com.

Learn more about this trial

Efficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With CCC

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