A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Therapy for Subjects With Mixed Dyslipidemia
Completed · Phase 3
Conditions studied: Mixed Dyslipidemia
In brief
The objective of the study is to assess the continued safety of the daily coadministration of ABT-335 in combination with rosuvastatin calcium, simvastatin or atorvastatin calcium.
Key facts
- Study ID
- NCT00491530
- Run by
- Abbott
- People needed
- 310
- Starts
- 2007-06-01
- Expected to finish
- 2008-11-01
- Last updated by the study team
- 2012-01-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult male and female subjects who voluntarily sign the informed consent.
- Subject has successfully completed the treatment phase of the preceding open-label year 1 study.
You may not qualify if…
- Subject is using or will use investigational medications, except as approved by Abbott.
- Subject has prematurely discontinued his/her combination therapy administered in the preceding open-label year 1 study.
Where it is running
- Medical Information Specialist — Abbott Park, Illinois, United States
Full record on ClinicalTrials.gov
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