Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04941599

2-Hydroxybenzylamine (2-HOBA) to Reduce HDL Modification and Improve HDL Function in Familial Hypercholesterolemia (FH)

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
72 (estimated)
Sponsor
Vanderbilt University Medical Center · Academic / Other
Sex
All
Age
18 Years – 69 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUG2-Hydroxybenzylamine2-Hydroxybenzylamine (2-HOBA) 250 mg three tabs TID (po) for 6 weeks.
OTHERPlaceboPlacebo 250 mg three tabs TID (po) for 6 weeks.

Timeline

Start date
2024-02-14
Primary completion
2026-06-30
Completion
2026-12-31
First posted
2021-06-28
Last updated
2026-02-04

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04941599. Inclusion in this directory is not an endorsement.