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Controlled Level EVERolimus in Acute Coronary Syndromes (CLEVER-ACS)

Primary Purpose

Acute Coronary Syndromes

Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
Everolimus
Placebo
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndromes focused on measuring Acute Coronary Syndromes, ST-Elevation Myocardial Infarction, Infarct size, inflammation, everolimus

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Elevation Myocardial Infarction (STEMI) as defined by:

    • ST-Elevation > 1mm in > 2 leads OR
    • Novel left bundle branch block (LBBB) OR
    • Posterior MI with ST-Depression > 1mm in > 2 leads
  2. Chest pain duration of > 10 minutes
  3. Primary Coronary Intervention (PCI) with drug-eluting stent (DES) within 24 hours of chest pain onset in the occluded culprit artery
  4. First Myocardial Infarction
  5. Occluded coronary artery at angiography specifically occlusion of one coronary vessel in the proximal third of either LAD, RCX or RCA, the mid segment of right coronary artery (RCA) or mid segment of a large left anterior descending (LAD) coronary artery, i.e. when the latter reaches the apex.
  6. Male and female patients 18 years to 90 years of age
  7. Signed informed consent

Exclusion Criteria:

  1. Participation in another drug or stent trial
  2. Pregnant women or nursing mothers
  3. Mechanical complication during acute coronary syndrome
  4. Scheduled PCI for additional lesion within 30 days
  5. Multivessel disease
  6. Major elective surgery planned in trial period
  7. Malignancy (unless healed or remission > 5 years)
  8. Chronic infection (HIV, Tbc, empyema)
  9. Severely compromised renal function (GFR< 30 ml/min)
  10. Positive PCR Test for SARS-CoV-2 and/or at least one positive answer to questions regarding symptoms/contact related to COVID-19.

Sites / Locations

  • Kerckhoff-Klinik, Department of Cardiology
  • University Hospital Chartié
  • University Hospital Duesseldorf
  • University Hospital Mainz
  • University Hospital Bern
  • University Hospital Geneva
  • Cardiocentro Ticino
  • University Hospital Zurich

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Everolimus

Placebo

Arm Description

Everolimus p.o. for 5 days (d0=7.5 mg, d1=7.5 mg, d2=7.5 mg, d3=5 mg, d4=5mg)

Placebo comparator with identical composition of tablets except everolimus

Outcomes

Primary Outcome Measures

Myocardial infarct size measured by MRI
To assess the effect of mTOR inhibition (everolimus) on myocardial infarct size as measured by MRI (Late Gadolinium Enhancement (LGE) for infarct size (transmurality) at 12-72 h (baseline) and 30 days

Secondary Outcome Measures

Microvascular obstruction (MVO) measured by MRI
To evaluate microvascular obstruction (MVO) by MRI at 12-72 h (baseline) and 30 days

Full Information

First Posted
February 3, 2012
Last Updated
December 2, 2021
Sponsor
University of Zurich
Collaborators
Swiss National Science Foundation, Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT01529554
Brief Title
Controlled Level EVERolimus in Acute Coronary Syndromes
Acronym
CLEVER-ACS
Official Title
Phase I-II Randomized Prospective Double-blind Multi-center Trial on the Effects of a Short Course of Oral Everolimus on Infarct Size, Left Ventricular Remodeling and Inflammation in Patients With Acute ST-Elevation Myocardial Infarction
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
January 8, 2015 (Actual)
Primary Completion Date
November 29, 2021 (Actual)
Study Completion Date
November 29, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
Swiss National Science Foundation, Novartis

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acute myocardial infarction (AMI) constitutes the major cause of death in most nations and death rates and morbidity remain substantial in the years thereafter. Inflammation is a hallmark throughout the distinct stages of atherosclerotic lesion formation preceding AMI as well as at the time of plaque rupture and during the post-infarct repair phase. Harnessing its harmful consequences constitutes an attractive therapeutic approach to address this unmet medical need. The objectives of this study are to evaluate the effects of mTOR inhibition (everolimus) on infarct size, myocardial function and inflammation in patients with ST-Elevation Myocardial Infarction. The efficacy objectives are: (1° endpoint): To assess the effect of mTOR inhibition (everolimus) on myocardial infarct size as change from baseline (12-72 hours after percutaneous coronary intervention) to 30 days follow-up measured by MRI (Late Gadolinium Enhancement (LGE) for transmurality). (2° endpoint): To evaluate microvascular obstruction (MVO) as change from baseline (12-72 hours after percutaneous coronary intervention) to 30 days follow-up evaluated by MRI. (3° endpoints): Change of left ventricular volume from baseline (12-72 hours after percutaneous coronary intervention) to 30 days follow-up measured by MRI. Change of biomarkers from time of coronary angiography to 30 days follow-up including a time-course (AUC). Biomarkers comprise hs-TnT, NT-proBNP, hs-CRP, IL-6 and inflammatory biomarkers OPG, sRANKL, OPN and CCN1. The safety objectives are: To explore the effect of mTOR inhibition (everolimus) on several clinical and safety laboratory parameters including plasma lipid levels and blood count. This will be complemented by analysis of inflammatory cell subsets in coronary thrombi and peripheral blood (CD4+ T helper lymphocyte subsets, monocyte subsets).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndromes
Keywords
Acute Coronary Syndromes, ST-Elevation Myocardial Infarction, Infarct size, inflammation, everolimus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Everolimus
Arm Type
Active Comparator
Arm Description
Everolimus p.o. for 5 days (d0=7.5 mg, d1=7.5 mg, d2=7.5 mg, d3=5 mg, d4=5mg)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo comparator with identical composition of tablets except everolimus
Intervention Type
Drug
Intervention Name(s)
Everolimus
Intervention Description
(d0=7.5 mg, d1=7.5 mg. d2=7.5 mg, d3=5 mg, d4=5mg)
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
matched placebo tablets manufactured to be identical to verum tablets except content of everolimus
Primary Outcome Measure Information:
Title
Myocardial infarct size measured by MRI
Description
To assess the effect of mTOR inhibition (everolimus) on myocardial infarct size as measured by MRI (Late Gadolinium Enhancement (LGE) for infarct size (transmurality) at 12-72 h (baseline) and 30 days
Time Frame
Change from baseline at 30 days
Secondary Outcome Measure Information:
Title
Microvascular obstruction (MVO) measured by MRI
Description
To evaluate microvascular obstruction (MVO) by MRI at 12-72 h (baseline) and 30 days
Time Frame
Change from baseline at 30 days
Other Pre-specified Outcome Measures:
Title
Left ventricular volume measured by MRI
Description
To evaluate left ventricular volume by MRI at 12-72 h (baseline) and 30 days
Time Frame
Change from baseline at 30 days
Title
Biomarkers
Description
To evaluate the changes of left ventricular volume from baseline
Time Frame
Change from baseline at 30 days including time course

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elevation Myocardial Infarction (STEMI) as defined by: ST-Elevation > 1mm in > 2 leads OR Novel left bundle branch block (LBBB) OR Posterior MI with ST-Depression > 1mm in > 2 leads Chest pain duration of > 10 minutes Primary Coronary Intervention (PCI) with drug-eluting stent (DES) within 24 hours of chest pain onset in the occluded culprit artery First Myocardial Infarction Occluded coronary artery at angiography specifically occlusion of one coronary vessel in the proximal third of either LAD, RCX or RCA, the mid segment of right coronary artery (RCA) or mid segment of a large left anterior descending (LAD) coronary artery, i.e. when the latter reaches the apex. Male and female patients 18 years to 90 years of age Signed informed consent Exclusion Criteria: Participation in another drug or stent trial Pregnant women or nursing mothers Mechanical complication during acute coronary syndrome Scheduled PCI for additional lesion within 30 days Multivessel disease Major elective surgery planned in trial period Malignancy (unless healed or remission > 5 years) Chronic infection (HIV, Tbc, empyema) Severely compromised renal function (GFR< 30 ml/min) Positive PCR Test for SARS-CoV-2 and/or at least one positive answer to questions regarding symptoms/contact related to COVID-19.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank Ruschitzka, Professor
Organizational Affiliation
UniversityHospitalZurich
Official's Role
Study Director
Facility Information:
Facility Name
Kerckhoff-Klinik, Department of Cardiology
City
Bad Nauheim
Country
Germany
Facility Name
University Hospital Chartié
City
Berlin
Country
Germany
Facility Name
University Hospital Duesseldorf
City
Düsseldorf
Country
Germany
Facility Name
University Hospital Mainz
City
Mainz
Country
Germany
Facility Name
University Hospital Bern
City
Bern
Country
Switzerland
Facility Name
University Hospital Geneva
City
Geneva
Country
Switzerland
Facility Name
Cardiocentro Ticino
City
Lugano
Country
Switzerland
Facility Name
University Hospital Zurich
City
Zurich
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
36049557
Citation
Stahli BE, Klingenberg R, Heg D, Branca M, Manka R, Kapos I, Muggler O, Denegri A, Kesterke R, Berger F, Stehli J, Candreva A, von Eckardstein A, Carballo D, Hamm C, Landmesser U, Mach F, Moccetti T, Jung C, Kelm M, Munzel T, Pedrazzini G, Raber L, Windecker S, Templin C, Matter CM, Luscher TF, Ruschitzka F. Mammalian Target of Rapamycin Inhibition in Patients With ST-Segment Elevation Myocardial Infarction. J Am Coll Cardiol. 2022 Nov 8;80(19):1802-1814. doi: 10.1016/j.jacc.2022.08.747. Epub 2022 Aug 29.
Results Reference
derived
PubMed Identifier
35092722
Citation
Klingenberg R, Stahli BE, Heg D, Denegri A, Manka R, Kapos I, von Eckardstein A, Carballo D, Hamm CW, Vietheer J, Rolf A, Landmesser U, Mach F, Moccetti T, Jung C, Kelm M, Munzel T, Pedrazzini G, Raber L, Windecker S, Matter CM, Ruschitzka F, Luscher TF. Controlled-Level EVERolimus in Acute Coronary Syndrome (CLEVER-ACS) - A phase II, randomized, double-blind, multi-center, placebo-controlled trial. Am Heart J. 2022 May;247:33-41. doi: 10.1016/j.ahj.2022.01.010. Epub 2022 Jan 28.
Results Reference
derived

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Controlled Level EVERolimus in Acute Coronary Syndromes

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