Cholesterol Lowering With EVOLocumab to Prevent Cardiac Allograft Vasculopathy in De-novo Heart Transplant Recipients

  • STATUS
    Recruiting
  • End date
    Jan 1, 2022
  • participants needed
    130
  • sponsor
    Lars Gullestad
Updated on 9 March 2021

Summary

The main goal of this study is to evaluate the effect of the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab on cardiac allograft vasculopathy in de novo heart transplant recipients.

Secondary objectives are to assess the impact of treatment on: i) cholesterol levels, ii) renal function, iii) inflammation, iv) quality of life, v) cardiac function as assessed by biomarkers and echocardiography, vi) the number of rejections, and (vii) safety and tolerability. As an exploratory outcome, the investigators will asses the effect of treatment on clinical events (death, myocardial infarction, cerebral stroke, cancer, end stage renal disease).

Description

Cardiac allograft vasculopathy is an important cause of morbidity and mortality in heart transplant recipients. Previous data show that, although clinical coronary artery disease often manifests years after heart transplantation, there are substantial changes in the coronary artery intima thickness over the first year after transplantation, suggesting that the adverse process starts shortly after transplantation. Moreover, the investigator's previous data have suggested that, whereas early intervention can prevent the long-term progression of cardiac allograft vasculopathy, the same intervention is less effective when administered late after heart transplantation. Thus, there seems to be a window of opportunity for preventive measures against cardiac allograft vasculopathy in de-novo transplant recipients.

The strong association between cholesterol levels and coronary heart disease in the general population, the high cholesterol levels in heart transplant recipients, the high prevalence of vasculopathy in the cardiac allograft, and the association between cholesterol levels and cardiac allograft vasculopathy together provide a strong rationale for aggressive cholesterol lowering in heart transplant recipients. Statins improve outcomes in heart transplant recipients, but their limited effect on post-transplant cholesterol levels, adverse effects, and drug interactions contribute to their not providing sufficient prophylaxis against post-transplant atherosclerotic disease.

Evolocumab is a well-tested drug with a favourable safety profile. It effectively reduces cholesterol levels on top of statin therapy in patients with coronary heart disease. The investigators hypothesise that evolocumab on top of statin therapy will significantly lower low density lipoprotein (LDL) levels in de novo heart transplant recipients. The investigators assume that this reduction in cholesterol levels will manifest as a reduced burden of cardiac allograft vasculopathy as measured by intracoronary ultrasound. Ultimately, the investigators believe that a reduced burden of vasculopathy will translate to reduced morbidity and long-term mortality in heart transplant recipients. The EVOLVD trial is a randomised, placebo-controlled, double-blind study designed to test the hypothesis that treatment with evolocumab can ameliorate cardiac allograft vasculopathy in heart transplant recipients.

Details
Condition Cardiac Allograft Vasculopathy
Treatment Placebo, Evolocumab
Clinical Study IdentifierNCT03734211
SponsorLars Gullestad
Last Modified on9 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients will be screened for eligibility during routine follow-up 4 - 8 weeks
after heart transplantation. All of the following conditions must apply prior
to administering the investigational medicinal product
Heart transplant recipient within the last 4 - 8 weeks
Age between 18 and 70 years
Informed consent obtained and documented according to Good Clinical Practice (GCP), and national/regional regulations
No contraindications to coronary angiography with intravascular ultrasound
Estimated glomerular filtration rate > 20 ml/min/1.73 m2 as assessed by the MDRD formula

Exclusion Criteria

Patients will be excluded from the study if they meet any of the following
criteria
Decompensated liver disease (Child-Pugh class C)
Severe renal failure, i.e. eGFR < 20 ml/min/1.73 m2 or on renal replacement therapy
Ongoing rejections or infections
Known sensitivity or intolerance to evolocumab or any of the excipients of Repatha
Prior use of PCSK9 inhibition treatment
Alcohol or drug abuse within 3 months of informed consent that would interfere with trial participation or any ongoing condition leading to decreased compliance with study procedures or study drug intake
Participation in another clinical trial involving an investigational drug and/or follow-up within 30 days prior to enrolment
Pregnancy
Female subject who has either (1) not used at least one highly effective method of birth control for at least 1 month prior to screening or (2) is not willing to use such a method during treatment and for an additional 15 weeks after the end of treatment, unless the subject is sterilised or postmenopausal
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