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Safety and Efficacy of Aliskiren in Post Myocardial Infarction Patients (ASPIRE)

5 juli 2012 bijgewerkt door: Novartis

A 36-week, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study Including a 2 Year Extension Study to Evaluate Efficacy and Safety of Aliskiren on the Prevention of Left Ventricular Remodeling in High Risk Post-acute Myocardial Infarction Patients When Added to Optimized Standard Therapy

The core and extension studies assessed the safety and efficacy of aliskiren when added to optimized standard therapy in patients that have had a high risk acute myocardial infarction (heart attack).

Studie Overzicht

Toestand

Voltooid

Conditie

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Werkelijk)

820

Fase

  • Fase 3

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

  • Argentinië
      • Novartis Argentina, Argentinië
        • Novartis Argentina
  • België
      • Novartis Belgium, België
        • Novartis Belgium
  • Canada
      • Novartis Canada, Canada
        • Novartis CANADA
  • Colombia
      • Bogota, Colombia
        • Novartis de Colombia S.A.
  • Denemarken
      • Novartis Denmark, Denemarken
        • Novartis Denmark
  • Duitsland
      • Novartis Germany, Duitsland
        • Novartis Germany
  • Hongarije
      • Budapest, Hongarije, H-1537
        • Novartis Hungary
  • Indië
      • Worli, Mumbai, Indië, 400018
        • Novartis Healthcare Private Limited
  • Israël
      • Petach Tikva, Israël, IL-49250
        • Novartis Pharma
  • Italië
      • Novartis Italy, Italië
        • Novartis Italy
  • Kalkoen
      • Istanbul, Kalkoen, TR-34353
        • Novartis Turkey
  • Korea, republiek van
      • Seoul, Korea, republiek van, 100-803
        • Novartis Korea Ltd.
  • Nederland
      • Novartis Netherlands, Nederland
        • Novartis Netherlands
  • Noorwegen
      • Novartis Norway, Noorwegen
        • Novartis Norway
  • Polen
      • Warszawa, Polen, PL-00-710-
        • Novartis Poland Sp. z o.o.
  • Russische Federatie
      • Novartis Russia, Russische Federatie
        • Novartis Russia
  • Slowakije
      • Bratislava, Slowakije, SK-821 09
        • Novartis Slovakia
  • Spanje
      • Novartis Spain, Spanje
        • Novartis Spain
  • Tsjechische Republiek
    • Praha 3
      • Praha, Praha 3, Tsjechische Republiek, CZ-130 00
        • Novartis Czech Republic
  • Venezuela
      • Caracas, Venezuela, 1062
        • Novartis de Venezuela, S.A.
  • Verenigd Koninkrijk
      • Novartis, Verenigd Koninkrijk
        • Novartis UK
  • Verenigde Staten
    • New Jersey
      • Novartis US, New Jersey, Verenigde Staten
        • Novartis US
  • Zweden
      • Novartis Sweden, Zweden
        • Novartis Sweden

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Core Study Inclusion Criteria:

  • Male or female patients 18 years and older.
  • Patients within 7-42 days of an acute myocardial infarction associated with left ventricular systolic dysfunction.
  • Documented left ventricular systolic dysfunction associated with the qualifying acute myocardial.

  • Patients must be on stable doses of the following concomitant medications for at least 2 weeks prior to Visit 1 unless contraindicated due to intolerance:

    • A Beta-blocker
    • An Anti-platelet agent
    • A Statin
    • An evidence-based dose of an Angiotensin Converting Enzyme Inhibitor (ACEI) or Angiotensin Receptor Blocker (ARB) but not both.
  • Qualifying Echocardiogram at Visit 1:

Core Study Exclusion Criteria:

  • Patients requiring both Angiotensin Converting Enzyme Inhibitor (ACEI) and Angiotensin Receptor Blocker (ARB) combination therapy at V1 or any time during the study.
  • Severe refractory hypertension defined as mean sitting systolic blood pressure (MSSBP) ≥ 180 mmHg and/or mean sitting diastolic blood pressure (MSDBP) ≥ 110 mmHg) at Visit 2.
  • Cardiogenic shock or systolic BP < 100 mmHg or diastolic < 60 mmHg within the 24 hours prior to Visits 1 or 2
  • Estimated Glomerular Filtration Rate (eGFR) < 30 ml/min/1.73m2 using the MDRD formula at Visit 1.
  • Stroke or transient ischemic event (TIA) within 6 months of Study Visit 1

Extension Study Inclusion Criteria:

  • Male or female patients who completed the core study through Visit 10 while on double-blind study drug
  • Patients who were able to participate in the study, and who consented to do so after the purpose and nature of the study had been clearly explained to them (written informed consent)

Extension Study Exclusion Criteria:

  • New York Heart Association (NYHA) class IV Congestive Heart Failure at Visit 1 (Core study Visit 10)
  • Symptomatic hypotension or reported systolic blood pressure (BP) < 90 mmHg within 24 hours prior to Visit 1 (Core study Visit 10)
  • Known Estimated Glomerular Filtration Rate (eGFR) < 30 mL/min/1.73m^2 using the Modification of Diet in Renal Disease (MDRD) formula at Visit 1 (Core study Visit 10)
  • Pregnant or nursing (lactating) women, where pregnancy was defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test (> 5 mIU/mL)
  • Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant Unless post-menopausal or using an acceptable method of contraception
  • Any surgical or medical condition that in the opinion of the investigator may place the patient at higher risk from his/her participation in the study or was likely to prevent the patient from complying with the requirements or completing the study

Other protocol-defined inclusion/exclusion criteria applied

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Dubbele

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Aliskiren

Core Study: Aliskiren ascending doses: 75 mg tablet for 1st week, 150 mg for 2nd week, 300 mg for next 34 weeks orally once daily in the morning.

Extension Study: Patients from both the core arms who completed core study and signed informed consent form were included in this arm of extension study.

Patients received 150 mg aliskiren tablet orally once a day for two weeks. Patients were then up-titrated to 300 mg aliskiren orally once a day at the discretion of the principal investigator based on their clinical condition for the duration of the study.
Geneesmiddel: Aliskiren
Aliskiren was available in 75 mg tablet, 150 mg tablet
Andere namen:
  • Tekturna®
Placebo-vergelijker: placebo
Core study: placebo for 36 weeks once daily in the morning
Geneesmiddel: placebo
Placebo tablets matching aliskiren for 36 weeks once daily in the morning for core period only.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Core Study: Change From Baseline in Left Ventricular End Systolic Volume (LVESV) as Measured by Echocardiography at End of Study.
Tijdsspanne: Baseline and final visit (after 26 to 36 weeks of treatment)
Change from baseline to end of study in left ventricular end systolic volume (LVESV) as measured by echocardiography. LVESV is a measurement of the volume of blood in the heart's left ventricular chamber at the end of the heart's contraction. This measurement was made by the echocardiography lab. LVESV values between 22 to 58 mL for men and 19-49 mL for women are considered normal. Baseline LVESV was a covariate.
Baseline and final visit (after 26 to 36 weeks of treatment)
Extension Study: Percentage of Participants With Deaths, Serious Adverse Events (SAEs), Discontinuation for Adverse Events (AEs) and Discontinuations for Abnormal Lab Values
Tijdsspanne: Extension study (24 weeks)
AEs are defined as any unfavorable and unintended diagnosis, symptom, sign (including an abnormal laboratory finding), syndrome or disease which either occurs during study, having been absent at baseline, or, if present at baseline, appears to worsen. Serious adverse events are any untoward medical occurrences that result in death, are life threatening, require (or prolong) hospitalization, cause persistent or significant disability/incapacity, result in congenital anomalies or birth defects, or are other conditions which in judgment of investigators represent significant hazards.
Extension study (24 weeks)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Core Study: Time to First Occurrence for the Composite Endpoints of Echocardiogram and Adjudicated Outcomes
Tijdsspanne: LVEF was measured at baseline and at final visit (after 26 to 36 weeks of treatment). Other endpoint components were assessed from randomization until the end of the study (week 36).
Composite outcome 1 included: Cardiovascular (CV) Death, hospitalization for heart failure (HF), or absolute reduction in Left Ventricular Ejection Fraction (LVEF) greater than 6%. Composite outcome 2 included: CV Death, hospitalization for HF, recurrent Myocardial Infarction, Stroke, or Resuscitated Sudden Death. LVEF was measured at baseline and final visit. All other events were adjudicated by a blinded external committee. Each composite endpoint analysis was based on (a) the percent of patients with that endpoint and (b) days in study to 1st event (or last exposure if no event occurred).
LVEF was measured at baseline and at final visit (after 26 to 36 weeks of treatment). Other endpoint components were assessed from randomization until the end of the study (week 36).
Core Study: Change From Baseline in Left Ventricular End Diastolic Volume (LVEDV)
Tijdsspanne: Baseline and final visit (after 26 to 36 weeks of treatment)
Change from baseline to end of study in left ventricular end diastolic volume (LVEDV) as measured by echocardiography. (LVEDV) is a measurement of the volume of blood in the heart's left ventricular chamber at the beginning of the chamber's filling with blood. This measurement was made by the echocardiography lab. LVEDV values between 67 to 155 mL for men and 56 to 104 mL for women are considered normal. Baseline LVEDV was a covariate.
Baseline and final visit (after 26 to 36 weeks of treatment)
Core Study: Change From Baseline in Left Ventricular Ejection Fraction (LVEF)
Tijdsspanne: Baseline and final visit (after 26 to 36 weeks of treatment )
Change from baseline to end of study in left ventricular ejection fraction (LVEF) (%) as measured by echocardiography. LVEF is the fraction of blood (in percent) pumped out of the heart's left ventricular chamber with each heart beat, and is a measure of cardiac output for the heart. This measurement was made by the echocardiography lab. Ejection fraction percentages > 55% are considered normal. Baseline LVEF was a covariate.
Baseline and final visit (after 26 to 36 weeks of treatment )
Core Study: Change From Baseline to End of Study in Infarction Segment Length (ISL) as Measured by Echocardiography
Tijdsspanne: Baseline and final visit (after 26 to 36 weeks of treatment)
Change from baseline to end of study in infarction segment length (ISL) (%) as measured by echocardiography. This is the length of the myocardial infarction segment as a percentage of the total cavity perimeter length as calculated by the echocardiography lab. Baseline ISL was a covariate.
Baseline and final visit (after 26 to 36 weeks of treatment)
Core Study: Change From Baseline to End of Study in Wall Motion Score (WMS) as Measured by Echocardiography
Tijdsspanne: Baseline and final visit (after 26 to 36 weeks of treatment)
Change from baseline to end of study in Wall Motion Score (WMS) as measured by echocardiography. WMS was obtained by examining multiple segments of the left ventricle and assigning each segment a score based on myocardial thickening: 1 for normal, 2 for hypokinetic; 3 for akinetic; and 4 for dyskinetic. The WMS was obtained as the average score for the segments visualized and was calculated by the echocardiography lab. Possible values range from 1 to 5. Higher scores are considered worse. Baseline WMS was a covariate.
Baseline and final visit (after 26 to 36 weeks of treatment)
Extension Study: Change From Baseline in Left Ventricular End Systolic Volume (LVESV) at Month 12
Tijdsspanne: Baseline(extension study), Month 12 (extension study)
Change from baseline to Month 12 in left ventricular end systolic volume (LVESV) as measured by echocardiography. LVESV is a measurement of the volume of blood in the heart's left ventricular chamber at the end of the heart's contraction. This measurement was made by the echocardiography lab. LVESV values between 22 to 58 mL for men and 19-49 mL for women are considered normal.
Baseline(extension study), Month 12 (extension study)
Extension Study: Change From Baseline in Left Ventricular End Diastolic Volume (LVEDV) at Month 12
Tijdsspanne: Baseline (extension study), Month 12 (extension study)
Change from baseline to Month 12 in left ventricular end diastolic volume (LVEDV) as measured by echocardiography. LVEDV is a measurement of the volume of blood in the heart's left ventricular chamber at the beginning of the chamber's filling with blood. This measurement was made by the echocardiography lab. LVEDV values between 67 to 155 mL for men and 56 to 104 mL for women are considered normal.
Baseline (extension study), Month 12 (extension study)
Extension Study: Change From Baseline in Left Ventricular Ejection Fraction (LVEF) at Month 12
Tijdsspanne: Baseline(extension study), Month 12 (extension study)
Change from baseline to Month 12 in left ventricular ejection fraction (LVEF) (%) as measured by echocardiography. LVEF is the fraction of blood (in percent) pumped out of the heart's left ventricular chamber with each heart beat, and is a measure of cardiac output for the heart. This measurement was made by the echocardiography lab. Ejection fraction percentages > 55% are considered normal.
Baseline(extension study), Month 12 (extension study)
Extension Study: Percentage of Participants With Orthostatic Blood Pressure Change
Tijdsspanne: Baseline (Day 0 Extension study), Week 2, Months 1, 3, 6, 9,16, 20, 24
Orthostatic blood pressure change is defined as a decrease of at least 20 mmHg in systolic blood pressure or a decrease of at least 10 mmHg in diastolic blood pressure when a patient moves from a sitting position to a standing position. A patient could show orthostatic blood pressure change at more than one visit. End of study is Month 24 or early discontinuation.
Baseline (Day 0 Extension study), Week 2, Months 1, 3, 6, 9,16, 20, 24
Extension Study: Percentage of Participants With Specified Criteria in Selected Labs by Laboratory Parameter
Tijdsspanne: 24 Months

Fasting blood samples were collected throughout the study and were analyzed at a central laboratory. Percentage of participants with the following clinically significant laboratory values are reported:

Potassium <3.5 mmol/L; Low value (Normal reference range: 3.5- 5.3)

Potassium >5.5 mmol/L and Potassium >6.0 mmol/L; High values (Normal reference range: 3.5-5.3)

Creatinine >176.8 μmol/L; High value (Normal reference range= Male: 62- 106 and Female 44- 80)

Blood Urea Nitrogen (BUN) >14.28; High value (Normal reference range: 2.1- 8.9)
24 Months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Novartis

Onderzoekers

  • Studie stoel: Novartis US, Novartis

Publicaties en nuttige links

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Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 december 2006

Primaire voltooiing (Werkelijk)

1 september 2009

Studie voltooiing (Werkelijk)

1 juli 2011

Studieregistratiedata

Eerst ingediend

19 december 2006

Eerst ingediend dat voldeed aan de QC-criteria

20 december 2006

Eerst geplaatst (Schatting)

21 december 2006

Updates van studierecords

Laatste update geplaatst (Schatting)

13 juli 2012

Laatste update ingediend die voldeed aan QC-criteria

5 juli 2012

Laatst geverifieerd

1 juli 2012

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • CSPP100A2340

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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