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Efficacy and Safety of PRC-4016 in Subjects With Mixed Dyslipidemia

NCT01972178 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 113

Last updated 2015-10-30

No results posted yet for this study

Summary

The objective of this study is

* To evaluate the efficacy of PRC-4016 by assessment of the percentage change in blood lipids and lipoprotein parameter from baseline after 12 weeks of treatment
* To evaluate the safety of PRC-4016 as assessed by adverse events and other safety parameters

Conditions

Interventions

DRUG

PRC-4016

DRUG

Placebo

DRUG

Statins

Any statin allowed (i.e. rosuvastatin, simvastatin, pravastatin, atorvastatin etc)

Sponsors & Collaborators

  • Pronova BioPharma

    lead INDUSTRY

Principal Investigators

  • Pål Nord, MD, MPH · Pronova BioPharma

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2014-07-31
Completion
2014-08-31

Countries

  • United States

Study Locations

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Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01972178 on ClinicalTrials.gov