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Effect of PCSK9 Inhibitors on Calcific Aortic Valve Stenosis

StatusRecruiting
PhasePhase 3
Started
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Record History

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  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Feb 2024 to Mar 22, 2024
    • Site details revised
    • Study title shortened, about 3 words
    v5
  2. Minor Start date: Jan 2024 to Feb 2024
    • Collaborators expanded, about 4 words
    • Study title expanded, about 3 words
    v4
  3. Notable Primary completion date: Dec 2023 to Dec 2027v3 Show 9 more changesShow less
    • Start date: Aug 1, 2021 to Jan 2024
    • Primary endpoint revised
    • Trial status: Recruiting to Not Yet Recruiting
    • Study completion date: Jan 2024 to Jan 2028
    • Interventions: PCSK9 inhibitor and Statin (Drug), Statin (Drug) to PCSK9 inhibitors and statins with or without ezetimibe (Drug), Statins with or without ezetimibe (Drug)
    • Eligibility criteria expanded, about 228 words
    • Secondary endpoints: 1 to 4
    • Study description shortened, about 375 words
    • Site details revised
  4. Notable Trial status: Not Yet Recruiting to Recruitingv2 Show 5 more changesShow less
    • Start date changed from estimate of Jul 2021 to Aug 1, 2021
    • Secondary endpoints: 2 to 1
    • Study description expanded, about 8 words
    • Site details revised
    • Eligibility criteria expanded, about 2 words
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Calcific aortic stenosis (CAS) can cause severe adverse cardiac events, but there are currently no effective drugs that can prevent or delay the progression of the disease. In fact, aortic valve replacement remains the only treatment option. CAS has been shown to be associated with Lp(a), LDL-C and PCSK9. Several observational studies indicated that the use of statins to decrease LDL-C levels was associated with the reduced incidence of CAS, but no randomized controlled trials (RCTs) showd that statins had any benefit on the progression of CAS. This may be related to the limited reduction of LDL-C by statin therapy. The proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have emerged as a new lipid-lowering drug. On the basis of statin therapy, PCSK9 inhibitors can further reduce LDL-C and Lp(a) levels by 50% to 60% and 20% to 30%, respectively. Some studies reported that elevated plasma PCSK9 levels were related to CAS and PCSK9 R46L loss-of-function mutation was associated with lower rates of CAS, and importantly, some observational studies found that PCSK9 inhibitors could reduce the incidence of CAS. Our trial aims to investigate the effect of PCSK9 inhibitors on preventing or delaying the progression of CAS. A total of 160 patients with mild or moderate CAS or asymptomatic severe AS will be randomly assigned to receive either statins or PCSK9 inhibitors+statins. All patients will be followed for at least 2 years at 3, 6,9,12,15,18,21,24 months after randomization. Quality of life (EQ-5D-3L including the EUROQOL visual analogue scale) questionnaires were gathered during each visit. Echocardiography and computer tomography were performed and blood samples were withdrawn at baseline, at 2 years visit, and before withdrawal from the study. The primary endpoint is the average annual change in peak aortic jet velocity on echocardiography. The secondary endpoints include average annual change in aortic valve area on echocardiography, average annual change in aortic valve calcification score on cardiac non-contrast computer tomography, heart valve surgery, change in quality-of-life scores, and average annual change in aortic and coronary artery calcification. Safety endpoints include all-cause death and cardiovascular events. The results of this trial will provide a new idea for the treatment of patients with CAS.
Trial Details
NCT Number NCT04968509
Lead Sponsor Beijing Anzhen Hospital
Collaborators: Beijing Municipal Health Commission
Conditions
(from sponsor)
Aortic Stenosis
Related terms Aortic Valve Stenosis, Aortic Valve, Calcification of
Enrollment 160 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov