Lp(a) Lowering Study of Pelacarsen (TQJ230) in Patients in the US With Elevated Lp(a) and Recent ACS (STEMI/NSTEMI) - Lp(a)FRONTIERS PEARL

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-79
SponsorNovartis Pharmaceuticals

About this trial

CTQJ230A1US13 is a randomized, double-blind, placebo-controlled, multicenter phase IIIb study designed to evaluate the efficacy, safety, tolerability, and coronary plaque effects of early pelacarsen (TQJ230) initiation in participants with elevated Lp(a) and recent acute coronary syndrome (ACS).

Eligibility criteria

Qualifiers

Lp(a) ≥ 150 nmol/L

Clinical syndrome consistent with spontaneous cardiac ischemia

Diagnosis of ACS: ST-elevation myocardial infarction (STEMI) or non-ST-elevation myocardial infarction (NSTEMI)

Disqualifiers

Uncontrolled hypertension

Heart failure New York Heart Association (NYHA) class IV

History of malignancy of any organs

History of hemorrhagic stroke or other major bleeding

Trial design

Treatments tested in this trial

  • Pelacarsen
  • Placebo

Treatment groups

240 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators