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Clinical Trial Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single- and multiple doses of ARO-APOC3 in healthy adult volunteers and in patients with severe hypertriglyceridemia and familial chylomicronemia syndrome (FCS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03783377
Study type Interventional
Source Arrowhead Pharmaceuticals
Contact
Status Completed
Phase Phase 1
Start date March 8, 2019
Completion date February 11, 2021

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