Study identifier:RDEA3170-111
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 1, Randomized, Open-Label, Study in Healthy Adult Male Subjects to Assess the Relative Bioavailability and Food Effect of Various Formulations of RDEA3170
Healthy
Phase 1
Yes
RDEA3170, 5mg, RDEA3170,10 mg, RDEA3170, 2.5 mg
Male
20
Interventional
18 Years - 65 Years
Allocation: Randomized
Endpoint Classification: Bio-availability Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Dec 2015 by Ardea Biosciences, Inc.
Ardea Biosciences, Inc.
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No locations available
Arms | Assigned Interventions |
---|---|
Experimental: RDEA3170 capsules or tablets 5 mg and 10 mg, 2.5 mg Treatment A: RDEA3170, 5 mg, administered in the fasted state. Treatment B: RDEA3170, 5 mg, administered in the fed state. Treatment C: RDEA3170, 10 mg, administered in the fasted state. Treatment D: RDEA3170, 10 mg, administered in the fed state. Treatment E: RDEA3170, 2.5 mg, administered as 10 mg in the fasted state. | - |