826358
Last Update Posted: 2012-09-28
Recruiting has ended
All Genders accepted | 18 Years-55 Years |
90 Estimated Participants | No Expanded Access |
Interventional Study | Accepts healthy volunteers |
Comparison of the Bioavailability of Fenofibric Acid and Rosuvastatin From 5/45 mg Strength of ABT-143 Relative to That From the Coadministration of ABT-335 (Fenofibric Acid) 45 mg and Rosuvastatin Calcium 5 mg
The purpose of this study is to evaluate the safety and compare the pharmacokinetic parameters from the fixed dose combination ABT-143 relative to that from the co-administration of the two monotherapies.
Eligibility
Relevant conditions:
Healthy
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Inclusion criteria
Exclusion criteria
locations
Contact Information
Overall Contact
No valid contacts available
Data sourced from ClinicalTrials.gov