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Clinical Trial Summary

The Investigators will test the hypothesis that 2-HOBA will reduce modification of HDL and LDL and improve HDL function in humans with heterozygous FH. The Investigators plan to first study subjects with Familial Hypercholesterolemia (FH), treating them with 750 mg of 2-HOBA or placebo every 8 hours for 6 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04941599
Study type Interventional
Source Vanderbilt University Medical Center
Contact Anca Ifrim, RN
Phone 6155224210
Email anca.ifrim@vumc.org
Status Recruiting
Phase Phase 2
Start date February 14, 2024
Completion date November 2025

See also
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