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Alirocumab and Reverse Cholesterol Transport

Primary Purpose

Atherosclerosis, Coronary Heart Disease

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Alirocumab
Placebos
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Atherosclerosis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy or with stable medical or surgical illnesses
  • LDL>100 mg/dl.

Exclusion Criteria:

  • Triglycerides>250
  • Taking drugs affecting lipid metabolism
  • Elevated liver function tests
  • Diabetes mellitus
  • A1c 6.5% or greater
  • Pregnant
  • Breastfeeding
  • Desire for conception in either sex.

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Alirocumab

Placebos

Arm Description

Subjects will receive alirocumab for 6 weeks.

Subjects will receive placebo for 6 weeks.

Outcomes

Primary Outcome Measures

Change from baseline in percent cholesterol excretion per day.
Percent cholesterol excretion per day is defined as the percent of endogenous rapidly-mixing cholesterol pools excreted per day into the stool.
Change from baseline in removal rate of esterified cholesterol from plasma per day.
The removal rate of esterified cholesterol from plasma per day is defined as fractional removal rate of esterified cholesterol from the plasma in pools/day.

Secondary Outcome Measures

Change from baseline in LDL cholesterol
Reduction in LDL with alirocumab treatment.
Change from baseline in percent cholesterol absorption
Percent cholesterol absorption is defined as the percent of intestinal cholesterol absorbed into the body.

Full Information

First Posted
December 6, 2016
Last Updated
November 5, 2018
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03014830
Brief Title
Alirocumab and Reverse Cholesterol Transport
Official Title
Effect of Alirocumab on Reverse Cholesterol Transport in Humans
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
June 4, 2018 (Actual)
Study Completion Date
July 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Alirocumab is an injectable treatment for elevated blood cholesterol. The hypothesis of this study is that it also increases cholesterol excretion from the body into the stool, a process sometimes called reverse cholesterol transport. A cholesterol metabolic study will be done before and after 6 weeks of alirocumab treatment. If alirocumab increases reverse cholesterol transport, it is possible that this action provides additional protection from cardiovascular disease.
Detailed Description
This study is a single-site, randomized, placebo-controlled clinical trial in which about 24 subjects are expected to complete an 8-week study period. The performance site is Washington University School of Medicine. Even though alirocumab is an approved drug, the investigators consider this to be a phase I trial because it is a physiological study in which the primary endpoint is change in fecal cholesterol excretion and measures of reverse cholesterol transport. It is not a treatment protocol and uses healthy subjects. Subjects with greater than ideal cholesterol but not taking cholesterol lowering drugs will be studied. All receive whole body cholesterol metabolism tests before and after treatment for 6 weeks with either alirocumab or placebo. Each test takes 2 weeks. On the first day the subjects receive about 35 mg cholesterol-d7 intravenously and blood samples are obtained in order to measure cholesterol turnover rate, pool size, esterification rate, transfer from HDL to LDL and removal from the plasma compartment. Fecal cholesterol excretion and related parameters are measured on days 13 and 14 after a relative steady-state is obtained. During this time the subjects consume a metabolic kitchen diet controlled in cholesterol and phytosterol content and consume oral tracer capsules consisting of cholesterol-d5 and sitostanol-d4. Plasma and stool samples are analyzed by gas chromatography/tandem mass spectrometry to determine daily percent cholesterol excretion from rapidly-mixing body cholesterol pools, fecal cholesterol mass and percent cholesterol absorption. The cholesterol metabolic test is repeated on day 43 and final measurements are made on day 57. Treatment effect, defined as the difference between active and placebo treatments is then calculated. Based on animal data it is expected that alirocumab will increase the efficiency of cholesterol excretion from body pools and the rate of removal of cholesterol ester from plasma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis, Coronary Heart Disease

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Alirocumab
Arm Type
Active Comparator
Arm Description
Subjects will receive alirocumab for 6 weeks.
Arm Title
Placebos
Arm Type
Placebo Comparator
Arm Description
Subjects will receive placebo for 6 weeks.
Intervention Type
Drug
Intervention Name(s)
Alirocumab
Other Intervention Name(s)
Praluent
Intervention Description
150 mg SQ every 2 weeks
Intervention Type
Drug
Intervention Name(s)
Placebos
Other Intervention Name(s)
Placebo
Intervention Description
Placebo injections SQ every 2 weeks
Primary Outcome Measure Information:
Title
Change from baseline in percent cholesterol excretion per day.
Description
Percent cholesterol excretion per day is defined as the percent of endogenous rapidly-mixing cholesterol pools excreted per day into the stool.
Time Frame
Measurements made on days 13-15 (baseline) and days 55-57 (on treatment).
Title
Change from baseline in removal rate of esterified cholesterol from plasma per day.
Description
The removal rate of esterified cholesterol from plasma per day is defined as fractional removal rate of esterified cholesterol from the plasma in pools/day.
Time Frame
Measurements made on days 1-3 (baseline) and days 43-45 (on treatment).
Secondary Outcome Measure Information:
Title
Change from baseline in LDL cholesterol
Description
Reduction in LDL with alirocumab treatment.
Time Frame
Measurements made on day 15 (baseline) and day 57 (on treatment).
Title
Change from baseline in percent cholesterol absorption
Description
Percent cholesterol absorption is defined as the percent of intestinal cholesterol absorbed into the body.
Time Frame
Measurements made on days 13-15 (baseline) and days 55-57 (on treatment).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy or with stable medical or surgical illnesses LDL>100 mg/dl. Exclusion Criteria: Triglycerides>250 Taking drugs affecting lipid metabolism Elevated liver function tests Diabetes mellitus A1c 6.5% or greater Pregnant Breastfeeding Desire for conception in either sex.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard E Ostlund, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plans to share individual data.

Learn more about this trial

Alirocumab and Reverse Cholesterol Transport

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