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

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-69
SponsorVanderbilt University Medical Center

About this trial

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.

Eligibility criteria

Qualifiers

Individuals with heterozygous Familial Hypercholesterolemia.

Disqualifiers

Myocardial infarction or stroke within the last 6 months

unstable angina, symptoms of angina within the last 3 months

NYHA class III or IV heart failure or LVEF < 30%

poorly controlled hypertension: SBP > 180 mm Hg or DBP > 110 mm Hg,

Trial design

Treatments tested in this trial

  • 2-Hydroxybenzylamine
  • Placebo

Treatment groups

72 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Vanderbilt University Medical Center

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator