drugset / Trial / NCT07223658

Study of ARO-DIMERPA in Adult Participants With Mixed Hyperlipidemia

NCT07223658 ↗

Phase 1/2 Recruiting 78 enrolled Arrowhead Pharmaceuticals
RandomizedSequentialQuadruple-blindTreatment

Summary

Study to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD), and effects on low-density lipoprotein cholesterol (LDL-C) and triglycerides (TGs) of single-dose ARO-DIMERPA and multiple doses of ARO-DIMERPA in adult participants with mixed hyperlipidemia.

Timeline

Start
2025-12-22
Primary completion
2026-09-30
Completion
2027-07

Drugs

EvaluationDrugModalityDoseRoute
Subject ARO-DIMERPA Unknown — Subcutaneous