drugset / Trial / NCT04606602

Study to Investigate Safety, Tolerability, PK and PD Response of SLN360 in Subjects With Elevated Lipoprotein(a)

NCT04606602 ↗

Phase 1 Completed 70 enrolled Silence Therapeutics GmbH Medpace, Inc. · collab
RandomizedParallel-groupDouble-blindPrevention

Summary

This study will investigate the safety and tolerability of SLN360 in patients with elevated Lp(a).

Timeline

Start
2020-11-18
Primary completion
2023-08-23
Completion
2023-08-23

Drugs

EvaluationDrugModalityDoseRoute
Subject zerlasiran Small interfering RNA (siRNA) 30 mg Subcutaneous
Subject zerlasiran Small interfering RNA (siRNA) 100 mg Subcutaneous
Subject zerlasiran Small interfering RNA (siRNA) 200 mg Subcutaneous
Subject zerlasiran Small interfering RNA (siRNA) 300 mg Subcutaneous
Subject zerlasiran Small interfering RNA (siRNA) 600 mg Subcutaneous
Subject zerlasiran Small interfering RNA (siRNA) 900 mg Subcutaneous