We enrolled 20 healthy volunteers, 18 to 65 years of age, with LDL-C levels >90 mg/dL. Subjects were recruited from internal clinical trial databases, advertisements, and postings at the Columbia University Medical Center (CUMC). Participants were not receiving lipid-lowering medications. All subjects of child-bearing capacity agreed to use birth control for the duration of the study and had a negative serum pregnancy test when applicable. This study was conducted in accordance with the principles of Good Clinical Practice and was approved by the CUMC Institutional Review Board. All study subjects provided written informed consent.
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