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Early Initiation of Tafolecimab for Patients With Acute Coronary Syndromeundergoing Percutaneous Coronary Intervention in Chinese Population

N

National Center for Cardiovascular Diseases

Status

Not yet enrolling

Conditions

Acute Coronary Syndrome
Non ST Segment Elevation Acute Coronary Syndrome

Treatments

Drug: Tafolecimab
Drug: Cholesterol Absorption Inhibitor
Drug: Statin

Study type

Interventional

Funder types

Other

Identifiers

NCT06096909
2021-CXGC03-002

Details and patient eligibility

About

For patients with ACS undergoing PCI, intensive lipid-lowering including PCSK9 monoclonal antibody should be started as soon as possible, that is, lower LDL-C level should be achieved as soon as possible. Compared with conventional lipid-lowering regimen, it is expected that the occurrence of major adverse cardiovascular events can still be reduced after drug discontinuation. Therefore, the optimization strategy of "for patients with ACS undergoing PCI, intensive lipid-lowering with PCSK9 monoclonal antibody can be started as soon as possible" is proposed.

Full description

Atherosclerotic cardiovascular disease (ASCVD) is the leading cause of death worldwide, and its incidence is increasing yearly in China, which has not yet reached the inflection point. Acute coronary syndrome (ACS) is a severe form of ASCVD, and lipid-lowering and antithrombotic therapy are the two core therapies. In the latest ESC/EAS guidelines for lipid management, for ACS patients, the target LDL-C is <1.4 mmol/L and ≥50% reduction from baseline, and specific initiatives to achieve this target are proposed, emphasizing the timing of clinical application and status of the novel lipid-lowering agent-proprotein convertase subtilisin/kexin type 9 monoclonal antibody (PCSK9) (hereafter referred to as PCSK9 antibody). In recent years, large-scale randomized controlled trials and outcomes of PCSK9 antibodies have demonstrated that PCSK9 antibodies further reduce adverse cardiovascular events by significantly lowering LDL-C levels under the background statin (±cholesterol absorption inhibitor ) therapy. The introduction of PCSK9 antibodies allowed for the reduction of LDL-C to unprecedented levels. From the "cholesterol principle" perspective, it is theoretically reasonable to add a PCSK9 inhibitor to statins as soon as possible during hospitalization for ACS patients. Still, there is no clear evidence from large RCTs. Current evidence supports that for ACS patients, PCSK9 antibodies could be used only when LDL-C is still not up to standard based on treatment with the maximum tolerable dose of statins during the first 2-3 months. However, the immediate initiation of PCSK9 antibodies during the acute phase of ACS (before hospital discharge) has yet to be studied.

Enrollment

3,684 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18 to 75 years;
  • clinical diagnosis with non-ST-segment elevation acute coronary syndrome (NSTE-ACS) ;
  • undergoing PCI
  • baseline LDL-C 1.8 mmol/L 3.4 mmol/L note: NSTE-ACS includes non-ST-elevation myocardial infarction and unstable angina.

Exclusion criteria

  • Severe heart failure (Killip III or IV) or cardiogenic shock;
  • Previous hemorrhagic cerebrovascular disease history;
  • Uncontrolled or recurrent arrhythmic events;
  • poorly controlled hypertension;
  • Severe hepatic and renal insufficiency (ALT/AST> 3 times upper limit of normal, eGFR<30 ml/kg/1.73m2, or ongoing dialysis) or creatine kinase elevation>5 times upper limit of normal
  • malignant tumor;
  • Intolerance to statins or cholesterol absorption inhibitors;
  • Intolerance to injections;
  • Life expectancy <1 year;
  • poor compliance.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

3,684 participants in 2 patient groups

experimental group
Experimental group
Description:
intensive lipid lowering therapy
Treatment:
Drug: Statin
Drug: Tafolecimab
control group
Active Comparator group
Description:
conventional lipid lowering therapy
Treatment:
Drug: Cholesterol Absorption Inhibitor
Drug: Statin

Trial documents
2

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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