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Completed Phase 2 Interventional Results available

Intensive Uric Acid Lowering With Verinurad and Febuxostat in Patients With Albuminuria

ClinicalTrials.gov ID: NCT03118739

Public ClinicalTrials.gov record NCT03118739. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 6:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Effects of Intensive Uric Acid Lowering Therapy With RDEA3170 (Verinurad) and Febuxostat in Patients With Albuminuria

Study identification

NCT ID
NCT03118739
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

  • Verinurad 9 mg+Febuxostat 80 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 17, 2017
Primary completion
Aug 12, 2018
Completion
Aug 12, 2018
Last update posted
Jan 9, 2020

2017 – 2018

United States locations

U.S. sites
18
U.S. states
2
U.S. cities
15
Facility City State ZIP Site status
Research Site Canyon Country California 91351
Research Site Chula Vista California 91911
Research Site Corona California 92882
Research Site Escondido California 92025
Research Site Lakewood California 90805
Research Site Lincoln California 95648
Research Site Los Angeles California 90017
Research Site Los Angeles California 90022
Research Site Los Angeles California 90036
Research Site North Hollywood California 91606
Research Site Oceanside California 92056-4510
Research Site Orange California 92868
Research Site Sacramento California 95821
Research Site Houston Texas 77058
Research Site Houston Texas 77070
Research Site Pearland Texas 77584
Research Site Sugar Land Texas 77478
Research Site Webster Texas 77598

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03118739, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 9, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03118739 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →