A Study to Assess the Effect of Intensive Uric Acid (UA) Lowering Therapy With RDEA3170, Febuxostat, Dapagliflozin on Urinary Excretion of UA

PHASE2CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

October 25, 2017

Primary Completion Date

July 19, 2018

Study Completion Date

July 19, 2018

Conditions
Asymptomatic Hyperuricemia
Interventions
DRUG

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

DRUG

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

DRUG

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

OTHER

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

Trial Locations (2)

21225

Research Site, Baltimore

91206

Research Site, Glendale

All Listed Sponsors
collaborator

Contract Research Organization: USA

UNKNOWN

collaborator

PAREXEL Early Phase Clinical Unit Baltimore

UNKNOWN

collaborator

PAREXEL Early Phase Clinical Unit-Los Angeles

UNKNOWN

collaborator

Clinical Laboratory: USA

UNKNOWN

collaborator

Harbor Hospital Laboratory

UNKNOWN

collaborator

GenX Laboratories Inc.

UNKNOWN

collaborator

Analytical Laboratory (Pharmacokinetic Sample Analysis): USA

UNKNOWN

collaborator

Covance Bioanalytical Services, LLC

UNKNOWN

lead

AstraZeneca

INDUSTRY