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Atherosclerotic Cardiovascular DiseaseNCT05639218

Impact of Optimal Pharmacotherapy on Lipid Profile and Qualitative Features of Atherosclerotic Plaques

An observational study of Atherosclerotic Cardiovascular Disease, run by Pauls Stradins Clinical University Hospital at 1 site in Latvia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Lipid accumulation, with mostly emphasized role of low-density lipoprotein cholesterol (LDL-C), is the pathogenetic cornerstone of atherosclerotic cardiovascular disease. Standard hypolipidemic therapy, based on statins and ezetimibe, does not always decrease LDL-C levels enough to achieve therapeutic goals. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Atherosclerotic Cardiovascular Disease
What is being tested?
Inclisiran
How many people
50 participants
Where
1 siteLatvia
Study dates
29 Jun 2021to Dec 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Study enrolled very high cardiovascular risk patients with established atherosclerotic cardiovascular disease, who receive PCSK9 inhibitors or inclisiran as add-on treatment to maximally tolerated statin dose and/or ezetimibe in the context of optimal pharmacotherapy, and in whom NIRS-IVUS has been performed in the Latvian Centre of Cardiology, Pauls Stradins Clinical University Hospital.

Who may be able to join

  • Very high cardiovascular risk - documented atherosclerotic cardiovascular disease
  • On maximally tolerated statin and/or ezetimibe therapy for at least 1 month LDL-C treatment target <1.4 mmol/l not achieved
  • Receiving PCSK9 inhibitor or inclisiran as add-on treatment to maximally tolerated statin dose and/or ezetimibe in the context of optimal pharmacotherapy
  • NIRS-IVUS performed (written informed consent for the procedure signed according to regulations in the hospital)
  • Available blood test results - plasma lipid profile
  • Patient agrees to participate in the study (signed informed consent)

Who cannot join

  • Not fulfilling any of inclusion criteria

Trial locations and contacts

1 site in 1 country.

Latvia1 site
  • Pauls Stradins Clinical University Hospital

    Riga, LV-1002

Other trials in Latvia

About this study

Official title: Impact of Optimal Pharmacotherapy on Plasma Lipid Profile and Qualitative Features of Atherosclerotic Plaques in Very-high Cardiovascular Risk Patients With Established Atherosclerotic Cardiovascular Disease

Lipid accumulation, with mostly emphasized role of low-density lipoprotein cholesterol (LDL-C), is the pathogenetic cornerstone of atherosclerotic cardiovascular disease. Standard hypolipidemic therapy, based on statins and ezetimibe, does not always decrease LDL-C levels enough to achieve therapeutic goals. A novel and promising direction is inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) in hepatocytes, subsequently reducing LDL-C receptor degradation and increasing intracellular LDL-C uptake.

Aim of this study is to evaluate the effect of optimal hypolipidemic pharmacotherapy, including PCSK9 inhibitors and inclisiran, on plasma lipid profile and qualitative features of atherosclerotic plaques in very-high cardiovascular risk patients.

Read more

This study enrolls patients with an established atherosclerotic cardiovascular disease, receiving PCSK9 inhibitors or inclisiran as add-on treatment to statins in maximally tolerated dose and/or ezetimibe.

Effect of hypolipidemic pharmacotherapy is evaluated by analysis of plasma lipid profile parameter changes and qualitative features of atherosclerotic plaques using Near-Infrared Spectroscopy Intravascular Ultrasound Imaging (NIRS-IVUS) method.

Results of the study would be sufficient for complementing evidence regarding therapeutic strategy in very-high cardiovascular risk patients.

Read the detailed description

Background:

Lipid accumulation in artery walls is the pathogenetic cornerstone of atherosclerosis. The most commonly studied risk factor of atherosclerotic cardiovascular disease is low-density lipoprotein cholesterol (LDL-C), nevertheless other plasma lipids have an established role as well. LDL-C is considered the primary target for cardiovascular risk reduction, with therapeutic goal <1.4 mmol/l in very-high cardiovascular risk patients with established atherosclerotic cardiovascular disease. Standard hypolipidemic therapy, based on statins and ezetimibe, is not always effective enough. Novel and promising direction is proprotein convertase subtilisin/kexin type 9 (PCSK9) - protease that binds LDL receptors in hepatocytes, subsequently promoting their lysosomal degradation. This process leads to reduced intracellular LDL-C uptake and increased LDL-C concentration in plasma. PCSK9 inhibitors - monoclonal antibodies evolocumab and alirocumab are successfully used in clinical practice, with a proven effectiveness in clinical trials ODYSSEY and FOURIER. An innovative medication is inclisiran - small interfering ribonucleic acid (siRNA) molecule that interferes with translation of messenger RNA (mRNA) of PCSK9 in hepatocytes as a result of complementary binding. Subsequently levels of synthesized PCSK9 are reduced, resulting in positive impact on plasma lipid profile. Inclisiran has demonstrated remarkable efficacy and safety profile in ORION clinical trials, being registered in European Medicines Agency since year 2020. Real-world data regarding optimal lipid-lowering pharmacotherapy, including experience with new medications, is of great clinical interest, studying effect on plasma lipid profile, as well as qualitative features of atherosclerotic plaques using Near-Infrared Spectroscopy Intravascular Ultrasound Imaging (NIRS-IVUS) method.

Aim:

Aim of this study is to evaluate effect of optimal hypolipidemic pharmacotherapy on plasma lipid profile and and qualitative features of atherosclerotic plaques in very-high cardiovascular risk patients receiving PCSK9 inhibitors or inclisiran as add-on treatment to statins in maximally tolerated dose and/or ezetimibe.

Study design:

Prospective observational study.

Study population:

Very-high cardiovascular risk patients with an established atherosclerotic cardiovascular disease, receiving PCSK9 inhibitors or inclisiran as add-on treatment to statins in maximally tolerated dose and/or ezetimibe in the context of optimal hypolipidemic pharmacotherapy, in whom NIRS-IVUS investigation has been performed.

Data acquisition:

Patients fulfilling eligibility criteria and agreeing to participate in the study are included. Baseline demographic and medical data is acquired, with subsequent follow-up ambulatory visits after 3 and 6 months after PCSK9 inhibitor or inclisiran therapy initiation. After 15 months since inclusion, follow-up with NIRS-IVUS performed is foreseen. For analysis of obtained data MS Excel and IBM SPSS Statistics software is used.

Clinical implications:

Results of this study would be of high clinical interest for complementing evidence and improving outcomes regarding therapeutic strategy in very-high cardiovascular risk patients with an established atherosclerotic cardiovascular disease.

Being tested
Inclisiran
Keywords
Atherosclerosis, PCSK9, Inclisiran, NIRS-IVUS, LDL-C
Medical subject headings
Atherosclerosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • InclisiranDrug

    Also called PCSK9 inhibitor

    Patients are receiving PCSK9 inhibitors or inclisiran in the context of optimal hypolipidemic pharmacotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. LDL-C level

    Plasma LDL-C level changes in patients receiving PCSK9 inhibitors or inclisiran

    Measured: 15 months

  2. Qualitative features of atherosclerotic plaques

    Changes in qualitative features of atherosclerotic plaques assessed by NIRS-IVUS investigation

    Measured: 15 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Dec 2022
  2. Study start29 Jun 2021
  3. Primary completion17 Feb 2023
  4. Study completionDec 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05639218
Sponsor's protocol ID
PCSK9I-0621
Status last verified
Nov 2023
First submitted
23 Nov 2022
Last updated
22 Nov 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Atherosclerotic Cardiovascular Disease, run by Pauls Stradins Clinical University Hospital at 1 site in Latvia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 22 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Latvia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

LDL-C level (time frame: 15 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Nov 2023.

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