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NCT00300482 · ClinicalTrials.gov registry record · Phase 3

Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calcium in Subjects With Multiple Abnormal Lipid Levels in the Blood

A Phase 3 study of Dyslipidemia and Coronary Heart Disease, sponsored by Abbott.

Completed
Registry status
Phase 3
Development phase
1,445
Enrollment target
1
Study location

NCT00300482 is a Phase 3 study of Dyslipidemia and Coronary Heart Disease that has completed, run by Abbott. The registered enrollment target is 1,445 participants, above the 327-participant average among 40 other Dyslipidemia trials with a reported enrollment target (342% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT00300482, a Phase 3 study of Dyslipidemia and Coronary Heart Disease, has completed, sponsored by Abbott.

COMPLETED
Registry status
Phase 3
Development phase
1,445 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to compare the safety and efficacy of fenofibric acid (ABT-335) + rosuvastatin calcium combination therapy with ABT-335 and rosuvastatin calcium monotherapy in subjects with multiple abnormal lipid levels in the blood.

Interventions

  • DRUG Placebo
  • DRUG ABT-335
  • DRUG Rosuvastatin Calcium

Study Locations (1)

Illinois

  • Global Medical Information - North Chicago

Trial Details

FieldValue
Enrollment Target 1,445 participants
Start Date 2006-03
Phase Phase 3

Sponsor

Abbott

181 total trials

What the Registry Record Tells You About NCT00300482

The ClinicalTrials.gov registry entry for NCT00300482 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 1,445 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 327-participant average among 40 other Dyslipidemia trials with a reported enrollment target (342% higher). The listed sponsor is Abbott, which has 181 total studies on file at ClinicalTrials.gov.

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

NCT00300482 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT00300482 about?

NCT00300482 is a clinical study titled "Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calcium in Subjects With Multiple Abnormal Lipid Levels in the Blood". The purpose of this study is to compare the safety and efficacy of fenofibric acid (ABT-335) + rosuvastatin calcium combination therapy with ABT-335 and rosuvastatin calcium monotherapy in subjects with multiple abnormal lipid levels in the blood.

What is the current status of trial NCT00300482?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,445 participants. The study started on 2006-03.

What conditions does trial NCT00300482 study?

This clinical trial studies the following conditions: Dyslipidemia, Coronary Heart Disease, Mixed Dyslipidemia.

What interventions are being tested in trial NCT00300482?

The interventions under investigation include: Placebo (DRUG), ABT-335 (DRUG), Rosuvastatin Calcium (DRUG).

Who is sponsoring clinical trial NCT00300482?

This trial is sponsored by Abbott, which has 181 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00300482 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.