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Study of ARO-APOC3 in Adults With Mixed Dyslipidemia — MUIR  

Mixed Dyslipidemia Clinical Trial

Official title:
A Double-Blind, Placebo-Controlled Phase 2b Study to Evaluate the Efficacy and Safety of ARO-APOC3 in Adults With Mixed Dyslipidemia

Clinical Trial Summary

Participants who have met all protocol eligibility criteria will be randomly assigned to treatment (ARO-APOC3 or placebo) in a double-blind fashion and will be evaluted for safety and efficacy over 48 weeks. Participants will be counseled to remain on a specified diet throughout the study, as recommended by the Investigator in accordance with local standard of care. After week 48, participants will be eligible and invited to consent and continue in an open-label extension study. All placebo participants who opt to continue will switch to active drug (ARO-APOC3) during the extension study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04998201
Study type Interventional
Source Arrowhead Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date September 28, 2021
Completion date August 14, 2023
View Details
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