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Not listed Phase 2 Interventional

Evaluation of ARI-3037MO, to Suppress LDL Cholesterol in Patients With Dyslipidemia

ClinicalTrials.gov ID: NCT02532218

Public ClinicalTrials.gov record NCT02532218. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 5:26 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized Evaluation of ARI-3037MO, to Suppress LDL Cholesterol in Patients With Dyslipidemia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to evaluate the efficacy and safety of ARI-3037MO compared to placebo in reducing low-density lipoprotein cholesterol (LDL-C) levels in subjects with dyslipidemia.

Study identification

NCT ID
NCT02532218
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Arisaph Pharmaceuticals Inc
Industry
Enrollment
176 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2015
Primary completion
Aug 31, 2016
Completion
Nov 30, 2016
Last update posted
Aug 7, 2016

2015 – 2016

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Catalina Reserch Institute, LLC Chino California 91710
S&W Clinical Reserch Fort Lauderdale Florida 33306
Jacksonville Center for Clinical Research Jacksonvile Florida 32216
Progressive Medical Research Port Orange Florida 32127
Sestron Clinical Research 833 Campbell Hill Street Suite 230 Marietta Georgia 30060
Midwest Institute for Clinical Research Indianapolis Indiana 46260
Louisville Metabolic and Atherosclerosis Research Center Louisville Kentucky 40213
Rochester clinical Research,Inc Rochester New York 14069
Sterling Research Group Ltd Cincinnati Ohio 45219
The Carl and Edyth Lindner Center for Reserch and education at the Christ Hospital Cincinnati Ohio 45219
Metabolic and atherosclerosis Research center Cincinnati Ohio 45227
IVA reserch Cincinnati Ohio 45245
Sterling Research group, Ltd Cincinnati Ohio 45246
Ohio Clinical Research-Lyndhurst Lyndhurst Ohio 44124
COR Clinical Research Oklahoma City Oklahoma 73103
Willamette Valley Clinical studies Eugene Oregon 97404
Health Research of Hampton Roads - Norfolk Norfolk Virginia 23502
National Clinical Research inc Richmond Virginia 23294
Raninier Clinical Reserach Renton Washington 98057

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02532218, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 7, 2016 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02532218 live on ClinicalTrials.gov.

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