36
Participants
Start Date
October 25, 2017
Primary Completion Date
July 19, 2018
Study Completion Date
July 19, 2018
Verinurad
Randomized patients will receive orally once daily fixed dose of verinurad in 2 treatment sequences AB or BA for 7 consecutive days. Treatment A: verinurad + febuxostat + dapagliflozin; Treatment B: verinurad + febuxostat + placebo
Febuxostat
Randomized patients will receive orally once daily fixed dose of febuxostat in 2 treatment sequences AB or BA for 7 consecutive days. Treatment A: verinurad + febuxostat + dapagliflozin; Treatment B: verinurad + febuxostat + placebo
Dapagliflozin
Randomized patients will receive orally once daily fixed dose of dapagliflozin in 2 treatment sequences AB or BA for 7 consecutive days. Treatment A: verinurad + febuxostat + dapagliflozin; Treatment B: verinurad + febuxostat + placebo
Dapagliflozin matched placebo
Randomized patients will receive orally once daily fixed dose of dapagliflozin matched placebo in 2 treatment sequences AB or BA for 7 consecutive days. Treatment A: verinurad + febuxostat + dapagliflozin; Treatment B: verinurad + febuxostat + placebo
Research Site, Baltimore
Research Site, Glendale
Lead Sponsor
Contract Research Organization: USA
UNKNOWN
PAREXEL Early Phase Clinical Unit Baltimore
UNKNOWN
PAREXEL Early Phase Clinical Unit-Los Angeles
UNKNOWN
Clinical Laboratory: USA
UNKNOWN
Harbor Hospital Laboratory
UNKNOWN
GenX Laboratories Inc.
UNKNOWN
Analytical Laboratory (Pharmacokinetic Sample Analysis): USA
UNKNOWN
Covance Bioanalytical Services, LLC
UNKNOWN
AstraZeneca
INDUSTRY