drugset / Trial / NCT07327840

Phase 2 Study of Kylo-11 in ASCVD Patients With Elevated Lp(a)

NCT07327840 ↗

Phase 2 Recruiting 204 enrolled Kylonova (Xiamen) Biopharma co., LTD.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a phase 2, double-blind, randomized, placebo-controlled, multi-center, dose-finding study to evaluate the efficacy and safety of Kylo-11 administered subcutaneously compared to placebo in participants with ASCVD and elevated Lp(a).

Timeline

Start
2025-10-29
Primary completion
2027-02-28
Completion
2028-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Kylo-11 Unknown — Subcutaneous