Clinical Trial

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

Recruiting Phase 2
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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).
Protocol Amendment History 1 change
notable Trial sites expanded: 43 -> 59 locations 2026-06-26
Trial Details
NCT Number NCT07327840
Lead Sponsor Kylonova (Xiamen) Biopharma co., LTD.
Conditions Lipoprotein Disorder
Enrollment 204 participants
Start Date 2025-10-29
Primary Completion 2027-02-28 (estimated)
Study Completion 2028-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-25