search
Back to results

Effect of Evolocumab Added to Moderate-Intensity Statin Therapy on LDL-C Lowering and Cardiovascular Adverse Events in Patients With Acute Coronary Syndrome (EMSIACS)

Primary Purpose

Acute Coronary Syndrome, Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitor

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Evolocumab
Sponsored by
Tianjin Chest Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring Acute Coronary Syndrome, Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitor, Lipid-lowering Drug, Major Cardiovascular Adverse Events

Eligibility Criteria

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

Inclusion Criteria:

  • Recent hospitalization for acute coronary syndrome: Complies with the diagnostic criteria for acute coronary syndrome (non-ST-segment elevation myocardial infarction, acute ST-segment elevation myocardial infarction, and unstable angina within 72 hours of onset)
  • LDL-C level (meet one of the following conditions):

    1. Prior to the study, patients who received intensive statins for more than 4 weeks (the same dose of statin therapy has been sustained for the past four weeks) with LDL-C levels ≥70 mg/dL (≥1.8 mmol/L) or non-HDL-C ≥100 mg /dL (≥2.6mmol/L) are included in the study;
    2. Prior to the study, patients who received moderate-intensity statin therapy for more than 4 weeks (the same dose of statin therapy has been sustained for the past four weeks) with LDL-C levels ≥90 mg/dL (≥2.3 mmol/L) or non-HDL-C≥ 120mg/dL (≥3.1mmol/L) are included in the study;
    3. Prior to the study, patients who do not receive statin therapy or who do not continue to receive statin with LDL-C ≥ 125 mg/dL (≥ 3.2 mmol/L) or non-HDL-C ≥ 155 mg/dL (≥ 4.0 mmol/L).
  • Being able to understand research requirements and sign informed consent

Exclusion Criteria:

  • Unstable clinical status (hemodynamics or ECG instability)
  • Uncontrolled arrhythmia, defined as recurrent or symptomatic ventricular tachycardia and atrial fibrillation with rapid ventricular reaction that the drug cannot control within three months prior to screening
  • Severe renal insufficiency, defined as estimated glomerular filtration rate<30ml/min/1.73m2
  • Active liver disease or liver dysfunction, whether it is on the patient's medical record or defined as an increase in alanine aminotransferase or aspartate aminotransferase more than 3 times above the upper limit of normal
  • Records on statin or rosuvastatin (any dose) intolerance or other statin intolerance
  • Known allergies to contrast agents, heparin, aspirin, ticagrelor or clopidogrel
  • Known allergies to the supplements required for the use of the drug
  • Patients who have been treated with evolocumab or other PCSK9 inhibitors
  • Received cholesterol ester transfer protein inhibitors treatment 12 months prior to screening
  • Received systemic steroid or cyclosporine treatment in the past 3 months
  • Known infections, hemorrhages, metabolic or endocrine disorders as determined by the researchers
  • Patients who have been included in other studies
  • Patients with active malignant tumor in need of treatment
  • Women with fertility (age <50 years, menstruation in the past 12 months), did not receive tubal ligation, oophorectomy or hysterectomy

Sites / Locations

  • Tianjin Chest Hospital,Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

the evolocumab plus statin therapy

the statin alone therapy

Arm Description

Patients with ACS are treated with atorvastatin (20mg) daily and evolocumab (140 mg) every two weeks throughout the study period

Patients with ACS are treated with atorvastatin (20mg) daily throughout the study period.

Outcomes

Primary Outcome Measures

Percent change in LDL-C

Secondary Outcome Measures

Major cardiovascular adverse events
Coronary heart disease death,nonfatal myocardial infarction,hospitalization for unstable angina,unplanned coronary revascularization, and stroke

Full Information

First Posted
September 21, 2019
Last Updated
November 20, 2020
Sponsor
Tianjin Chest Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT04100434
Brief Title
Effect of Evolocumab Added to Moderate-Intensity Statin Therapy on LDL-C Lowering and Cardiovascular Adverse Events in Patients With Acute Coronary Syndrome
Acronym
EMSIACS
Official Title
Effect of Evolocumab Added to Moderate-Intensity Statin Therapy on LDL-C Lowering and Cardiovascular Adverse Events in Patients With Acute Coronary Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Anticipated)
Primary Completion Date
June 1, 2022 (Anticipated)
Study Completion Date
June 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tianjin Chest Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study is an open-label, multicenter, and randomized study(five hospitals).The purpose of this study is to assess the differences in the effects of the evolocumab added to moderate-intensity statin therapy and the moderate-intensity statin only therapy on the regulation of LDL-C levels in patients with acute phase acute coronary syndrome after four weeks of treatment. The primary outcome is the percentage change in LDL-C in weeks 4 and week 12 after treatment. The secondary outcome is the occurrence of MACE after 12 weeks and 1 year of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome, Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitor
Keywords
Acute Coronary Syndrome, Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitor, Lipid-lowering Drug, Major Cardiovascular Adverse Events

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
the evolocumab plus statin therapy
Arm Type
Experimental
Arm Description
Patients with ACS are treated with atorvastatin (20mg) daily and evolocumab (140 mg) every two weeks throughout the study period
Arm Title
the statin alone therapy
Arm Type
No Intervention
Arm Description
Patients with ACS are treated with atorvastatin (20mg) daily throughout the study period.
Intervention Type
Drug
Intervention Name(s)
Evolocumab
Intervention Description
Patients were randomly assigned of the ratio of 1:1 using a computer-generated random number and divided into two treatment groups: the statin alone therapy and the evolocumab plus statin therapy.
Primary Outcome Measure Information:
Title
Percent change in LDL-C
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Major cardiovascular adverse events
Description
Coronary heart disease death,nonfatal myocardial infarction,hospitalization for unstable angina,unplanned coronary revascularization, and stroke
Time Frame
4 weeks and 1 year
Other Pre-specified Outcome Measures:
Title
The mean percentage change from baseline in LDL-C levels
Time Frame
within 1 year
Title
The proportion of patients with LDL-C <70 mg/dL during treatment
Time Frame
week 4 and week 12
Title
the quality of life of patients
Description
using EQ-5D-3L questionnaire score to assess the quality of life
Time Frame
week 12 and week 48
Title
The effect of evolocumab on platelet function based on the area under curve
Description
using Col/ADP test to evaluate platelet function
Time Frame
from baseline to 72 hours and baseline to week 4
Title
the effect of evolocumab on the percentage change of inflammatory markers (high-sensitivity C-reactive protein)
Time Frame
from baseline to week 48

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Recent hospitalization for acute coronary syndrome: Complies with the diagnostic criteria for acute coronary syndrome (non-ST-segment elevation myocardial infarction, acute ST-segment elevation myocardial infarction, and unstable angina within 72 hours of onset) LDL-C level (meet one of the following conditions): Prior to the study, patients who received intensive statins for more than 4 weeks (the same dose of statin therapy has been sustained for the past four weeks) with LDL-C levels ≥70 mg/dL (≥1.8 mmol/L) or non-HDL-C ≥100 mg /dL (≥2.6mmol/L) are included in the study; Prior to the study, patients who received moderate-intensity statin therapy for more than 4 weeks (the same dose of statin therapy has been sustained for the past four weeks) with LDL-C levels ≥90 mg/dL (≥2.3 mmol/L) or non-HDL-C≥ 120mg/dL (≥3.1mmol/L) are included in the study; Prior to the study, patients who do not receive statin therapy or who do not continue to receive statin with LDL-C ≥ 125 mg/dL (≥ 3.2 mmol/L) or non-HDL-C ≥ 155 mg/dL (≥ 4.0 mmol/L). Being able to understand research requirements and sign informed consent Exclusion Criteria: Unstable clinical status (hemodynamics or ECG instability) Uncontrolled arrhythmia, defined as recurrent or symptomatic ventricular tachycardia and atrial fibrillation with rapid ventricular reaction that the drug cannot control within three months prior to screening Severe renal insufficiency, defined as estimated glomerular filtration rate<30ml/min/1.73m2 Active liver disease or liver dysfunction, whether it is on the patient's medical record or defined as an increase in alanine aminotransferase or aspartate aminotransferase more than 3 times above the upper limit of normal Records on statin or rosuvastatin (any dose) intolerance or other statin intolerance Known allergies to contrast agents, heparin, aspirin, ticagrelor or clopidogrel Known allergies to the supplements required for the use of the drug Patients who have been treated with evolocumab or other PCSK9 inhibitors Received cholesterol ester transfer protein inhibitors treatment 12 months prior to screening Received systemic steroid or cyclosporine treatment in the past 3 months Known infections, hemorrhages, metabolic or endocrine disorders as determined by the researchers Patients who have been included in other studies Patients with active malignant tumor in need of treatment Women with fertility (age <50 years, menstruation in the past 12 months), did not receive tubal ligation, oophorectomy or hysterectomy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jing Gao, PHD
Phone
+86-13820156072
Email
gaojing2088@163.com
Facility Information:
Facility Name
Tianjin Chest Hospital,
City
Tianjin
ZIP/Postal Code
300222
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
JING GAO, PH.D
Phone
13820156072
Email
gaojing2088@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34887772
Citation
Gao J, Liu JY, Lu PJ, Xiao JY, Gao MD, Li CP, Cui Z, Liu Y. Effects of Evolocumab Added to Moderate-Intensity Statin Therapy in Chinese Patients With Acute Coronary Syndrome: The EMSIACS Trial Study Protocol. Front Physiol. 2021 Nov 23;12:750872. doi: 10.3389/fphys.2021.750872. eCollection 2021.
Results Reference
derived

Learn more about this trial

Effect of Evolocumab Added to Moderate-Intensity Statin Therapy on LDL-C Lowering and Cardiovascular Adverse Events in Patients With Acute Coronary Syndrome

We'll reach out to this number within 24 hrs