Safety Study to Evaluate the Effects of Mild and Moderate Renal Impairment on the Pharmacokinetics of ABT-335 and Rosuvastatin When Administered Concomitantly
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
37
45 mg once daily for 10 consecutive days
10 mg once daily for 10 days
Site Reference ID/Investigator# 6610
Gainesville, Florida, United States
Site Reference ID/Investigator# 6738
Miami, Florida, United States
Site Reference ID/Investigator# 7723
Minneapolis, Minnesota, United States
Site Reference ID/Investigator# 7319
Knoxville, Tennessee, United States
Blood concentrations of the active ingredients and metabolites of ABT-335 and rosuvastatin
Time frame: Days 1, 8, 9, and 10
Safety and tolerability of the study drugs
Time frame: Study duration
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Site Reference ID/Investigator# 6928
San Antonio, Texas, United States
Site Reference ID/Investigator# 8280
Richmond, Virginia, United States