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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorChina National Center for Cardiovascular Diseases

About this trial

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.

Eligibility criteria

Qualifiers

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.

Disqualifiers

Severe heart failure (Killip III or IV) or cardiogenic shock;

Previous hemorrhagic cerebrovascular disease history;

Uncontrolled or recurrent arrhythmic events;

poorly controlled hypertension;

Trial design

Treatments tested in this trial

  • Tafolecimab
  • Cholesterol Absorption Inhibitor
  • Statin

Treatment groups

3,684 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators