drugset / Trial / NCT05563246

A Study of LY3473329 in Adult Participants With Elevated Lipoprotein(a) at High Risk for Cardiovascular Events

NCT05563246 ↗

Phase 2 Completed 233 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to evaluate the efficacy and safety of LY3473329 in adult participants with elevated Lp(a) at high risk for cardiovascular events.

Timeline

Start
2022-11-24
Primary completion
2024-03-14
Completion
2024-03-14

Outcome

Met primary endpoint

registry analysis (superiority test); 10 mg LY3473329 vs Placebo; p <.001; LS Mean Difference (Final Values) -47.61 (95% CI -57.68 to -35.14); Mixed Models Analysis NCT05563246 ↗

registry analysis (superiority test); 10 mg LY3473329 vs Placebo; p <.001; LS Mean Difference (Final Values) -40.38 (95% CI -50.45 to -28.27); Mixed Models Analysis NCT05563246 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Muvalaplin Small molecule 10 mg Oral
Subject Muvalaplin Small molecule 60 mg Oral
Subject Muvalaplin Small molecule 240 mg Oral

Indications

No indication recorded.