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Clinical Trials/EUCTR2017-003236-37-IT
EUCTR2017-003236-37-IT
Active, not recruiting
Phase 1

High-Resolution Assessment of Coronary Plaques in a Global Evolocumab Randomized Study (HUYGENS) - NA

AMGEN INC.0 sites150 target enrollmentSeptember 2, 2021

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Dyslipidemia
Sponsor
AMGEN INC.
Enrollment
150
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 2, 2021
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
AMGEN INC.

Eligibility Criteria

Inclusion Criteria

  • Key Inclusion Criteria
  • Age \= 18 years at screening.
  • Clinical indication for coronary angiography during admission due to NSTE\-ACS with interventional treatment of culprit plaque.
  • LDL\-C level via local lab assessment based on statin use at screening:
  • \- No statin use: \= 130 mg/dL
  • \- Low\- or moderate\-intensity statin use: \= 80 mg/dL
  • \- High\-intensity statin use: \= 60 mg/dL
  • On maximally tolerated statin therapy in accordance with standard of care per local guidelines prior to randomization.
  • Tolerates placebo run\-in injection at screening.
  • Meet all the following criteria at the qualifying coronary angiogram:

Exclusion Criteria

  • Subjects are excluded from the study if any of the following criteria apply.
  • Disease Related:
  • \-ST\-segment elevation myocardial infarction (STEMI) or left bundle branch block (LBBB).
  • \-ACS likely to be caused by a non\-atherosclerotic process, in the opinion of the investigator (ie, type 2 myocardial infarction, which is characterized by an imbalance between myocardial oxygen demand and supply).
  • \-Clinically significant heart disease which in the opinion of the investigator is likely to require coronary bypass surgery, PCI (does not apply to PCI of non STEMI (NSTEMI) during initial screening angiogram), surgical or percutaneous valve repair and/or replacement during the course of the study.
  • \-Any cardiac surgery within 6 weeks prior to screening.
  • Diagnostic Assessments
  • \-Triglycerides \= 400 mg/dL (4\.5 mmol/L) at screening.
  • \-Moderate to severe renal dysfunction, defined as an estimated glomerular filtration rate (eGFR) \< 30 mL/min/1\.73m2 at screening.
  • Other Medical Conditions

Outcomes

Primary Outcomes

Not specified

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