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
| Type | Name | Description |
|---|---|---|
| DRUG | 2-Hydroxybenzylamine | 2-Hydroxybenzylamine (2-HOBA) 250 mg three tabs TID (po) for 6 weeks. |
| OTHER | Placebo | Placebo 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04941599. Inclusion in this directory is not an endorsement.