Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Febuxostat Versus Allopurinol or Placebo in Patients With Hyperuricosuria and Calcium Oxalate Stones

ClinicalTrials.gov ID: NCT01077284

Public ClinicalTrials.gov record NCT01077284. 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, 1:30 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

A Multicenter, Randomized, Double-Blind, Placebo and Allopurinol Controlled, Phase 2 Study to Evaluate Febuxostat in the Medical Management of Subjects With Hyperuricosuria and Calcium Oxalate Stones

Study identification

NCT ID
NCT01077284
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Takeda
Industry
Enrollment
99 participants

Conditions and interventions

Interventions

  • Febuxostat Drug
  • Allopurinol Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jan 31, 2010
Primary completion
Oct 31, 2011
Completion
Oct 31, 2011
Last update posted
Feb 14, 2013

2010 – 2011

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Anchorage Alaska
Not listed Tucson Arizona
Not listed Costa Mesa California
Not listed Orange California
Not listed Palmdale California
Not listed Poway California
Not listed Rancho Cucamonga California
Not listed San Diego California
Not listed Santa Ana California
Not listed Denver Colorado
Not listed New Britain Connecticut
Not listed Miami Florida
Not listed Augusta Georgia
Not listed Honolulu Hawaii
Not listed Boise Idaho
Not listed Meridian Idaho
Not listed Lexington Kentucky
Not listed Kalamazoo Michigan
Not listed Jackson Mississippi
Not listed Albuquerque New Mexico
Not listed New Windsor New York
Not listed Shelby North Carolina
Not listed Wilmington North Carolina
Not listed East Providence Rhode Island
Not listed Dallas Texas
Not listed Houston Texas
Not listed Sugar Land Texas

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 NCT01077284, 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 Feb 14, 2013 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01077284 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →