drugset / Trial / NCT00808678

Comparison of the Bioavailability of Fenofibric Acid and Rosuvastatin From ABT-143 Relative to That From the Coadministration of ABT-335 (Fenofibric Acid) and Rosuvastatin Calcium

NCT00808678

Phase 1 Completed 90 enrolled AstraZeneca
RandomizedCrossoverOpen-labelTreatment

Summary

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.

Timeline

Start
2008-12
Primary completion
2009-01
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject ABT-143 Unknown 20 mg
Subject ABT-143 Unknown 135 mg
Comparator ABT-335 Small molecule 135 mg
Comparator Rosuvastatin Small molecule 20 mg

Indications

No indication recorded.