drugset / Trial / NCT06813911

Lp(a) Lowering Study of Pelacarsen (TQJ230) With Background Inclisiran in Participants With Elevated Lp(a) and Established ASCVD

NCT06813911

Phase 3 Recruiting 340 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study CTQJ230A12304, is to evaluate the efficacy, safety, and tolerability of pelacarsen (TQJ230) compared to placebo in participants with ASCVD who have elevated lipoprotein(a) (Lp(a)), and who are on background inclisiran treatment for elevated low-density lipoprotein cholesterol (LDL-C).

Timeline

Start
2025-04-30
Primary completion
2028-02-03
Completion
2028-02-29

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pelacarsen Antisense oligonucleotide 80 mg Subcutaneous
Comparator Inclisiran Small interfering RNA (siRNA)