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NCT00504829 · ClinicalTrials.gov registry record · Phase 2

Study of Atorvastatin/Fenofibrate (LCP-AtorFen) Combination Therapy in Dyslipidemia

A Phase 2 study of Dyslipidemia, sponsored by Veloxis Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
220
Enrollment target
1
Study location

NCT00504829: Completed Phase 2 study of Dyslipidemia, sponsored by Veloxis Pharmaceuticals.

NCT00504829 is a Phase 2 study of Dyslipidemia that has completed, run by Veloxis Pharmaceuticals. The registered enrollment target is 220 participants, below the 358-participant average among 40 other Dyslipidemia trials with a reported enrollment target (39% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00504829, a Phase 2 study of Dyslipidemia, has completed, sponsored by Veloxis Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
220 participants
Enrollment target
1
Study location

Study Summary

The current study is designed to test the efficacy, safety and tolerability of LCP-AtorFen, a combination of atorvastatin and fenofibrate.

Primary Outcome

Mean percent change from baseline to end-of-treatment (12 weeks) for non-HDL cholesterol and triglycerides and the mean percent change from baseline to end-of-treatment for HDL cholesterol for AtorFen 40/100mg fixed-dose combination tablet versus atorvastatin 40mg tablet.

Conditions Studied

Interventions

  • DRUG atorvastatin
  • DRUG fenofibrate
  • DRUG LCP-AtorFen

Study Locations (1)

Illinois

  • Radiant Research, 515 N State Street, Suite 2700 - Chicago

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2007-07
Est. Completion 2008-07
Phase Phase 2
Veloxis Pharmaceuticals

15 total trials

What the finished NCT00504829 record still lists

NCT00504829 is an interventional study that assigns participants to a tested intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap, below the 358-participant average among 40 other Dyslipidemia trials with a reported enrollment target (39% lower).

The record links to 1 condition, with Dyslipidemia appearing as the primary indexed condition, and to 3 interventions - of which atorvastatin is the first listed.

NCT00504829 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT00504829 about?

NCT00504829 is a clinical study titled "Study of Atorvastatin/Fenofibrate (LCP-AtorFen) Combination Therapy in Dyslipidemia". The current study is designed to test the efficacy, safety and tolerability of LCP-AtorFen, a combination of atorvastatin and fenofibrate.

What is the current status of trial NCT00504829?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 220 participants. The study started on 2007-07. Estimated completion is 2008-07.

What conditions does trial NCT00504829 study?

This clinical trial studies the following conditions: Dyslipidemia.

What interventions are being tested in trial NCT00504829?

The interventions under investigation include: atorvastatin (DRUG), fenofibrate (DRUG), LCP-AtorFen (DRUG).

Who is sponsoring clinical trial NCT00504829?

This trial is sponsored by Veloxis Pharmaceuticals, which has 15 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00504829 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Dyslipidemia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00504829's enrollment target sits among peer trials

220 13th of 40 higher than 28 of 40 other Dyslipidemia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Dyslipidemia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00504829, the US trial registry maintained by the National Library of Medicine. NCT00504829 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.