Phase 1
N=101
A Study of Evacetrapib in Participants With Abnormal Cholesterol
Dyslipidemia
Bottom Line
View on ClinicalTrials.gov: NCT02168803 ↗Enrolled (actual)
101
Serious AEs
2.5%
Results posted
Oct 2018
Primary outcome: Primary: Pharmacokinetics (PK) Parameters of Evacetrapib: Area Under the Concentration Versus Time Curve From Time Zero to the Last Time Point With a Measurable Concentration (AUC[0-tlast]) — 14200; 37400; 36900; 44400 nanogram∙hour/mililliter (ng∙h/mL)
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- Evacetrapib (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Eli Lilly and Company
- Primary completion
- Dec 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pharmacokinetics (PK) Parameters of Evacetrapib: Area Under the Concentration Versus Time Curve From Time Zero to the Last Time Point With a Measurable Concentration (AUC[0-tlast]) |
14200; 37400; 36900; 44400 | — |
| PRIMARY PK Parameters of Evacetrapib: Maximum Concentration (Cmax) |
1020; 1690; 1770; 1850 | — |
| PRIMARY PK Parameters of Evacetrapib: Terminal Half-life |
52.5 | — |
| SECONDARY PD Parameters of Evacetrapib: High Density Lipoprotein Cholesterol (HDL-C) Level |
1.538; 1.562; 1.670; 1.724; 1.777; 1.772 | — |
| SECONDARY PD Parameters of Evacetrapib: Low-Density Lipoprotein Cholesterol (LDL-C) Level |
3.711; 3.359; 3.662; 3.173; 3.152; 3.293 | — |
| SECONDARY PD Parameters of Evacetrapib: Total Cholesterol Level |
5.922; 5.523; 6.015; 5.577; 5.531; 5.715 | — |
| SECONDARY PD Parameters of Evacetrapib: Triglyceride Level |
1.474; 1.311; 1.485; 1.482; 1.309; 1.419 | — |
Summary
The main purpose of this study is to measure how much of the drug gets into the blood stream and how long it takes the body to get rid of it when given once a day for 12, 24, and 52 weeks to participants with abnormal amounts of cholesterol and/or fat in the blood stream. Information about any side effects that may occur will also be collected.
This study will also evaluate how the study drug reacts in the body when given once a day for 12, 24 and 52 weeks and how the body responds and returns to normal when the treatment is complete. The relationship between study drug and the results from the how the study drug reacts in the body may be explored, if needed.
Eligibility Criteria
Inclusion Criteria
- Generally healthy participants or have stable medical conditions that, in the investigator's opinion, will not significantly alter the disposition of the drug, will not place the participant at increased risk by participating in the study, and will not interfere with interpretation of the data and meets one of the following criteria:
- Elevated low-density lipoprotein cholesterol (LDL-C) greater than 100 milligrams per deciliter (mg/dL), OR
- Low high-density lipoprotein cholesterol (HDL-C) less than 45 mg/dL (men); less than 50 mg/dL (women), OR
- Hypercholesterolemia on stable statin therapy for at least 3 month
- Have a body mass index (BMI) of 18 to 37 kilograms per square meter (kg/m^2), inclusive, at screening
Exclusion Criteria
- Have known allergies or intolerance to evacetrapib, related compounds
- Have history of recurrent rashes or chronic skin conditions
- Have significant history of or current chronic, active inflammatory conditions
- Have history or current evidence of significant neurological disorder
- Have long-standing diabetes that is insulin requiring
- Have history of or current symptoms of malabsorption syndromes, history of gastric bypass surgery
Data sourced from ClinicalTrials.gov (NCT02168803). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.