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Completed Phase 2 Interventional

Study to Evaluate sUA Lowering Activity, Safety and Efficacy of Oral Ulodesine Added to Allopurinol

ClinicalTrials.gov ID: NCT01265264

Public ClinicalTrials.gov record NCT01265264. 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 Oct 27, 2026, 8:37 PM 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 Randomized, Double-Blind, Dose-Response Study of the Safety and Efficacy of Oral Ulodesine Added to Allopurinol in Subjects With Gout Who Have Not Adequately Responded to Allopurinol Monotherapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether ulodesine and allopurinol combined for 12 weeks are effective in treating gout in patients who are not adequately responding to allopurinol alone.

Study identification

NCT ID
NCT01265264
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
BioCryst Pharmaceuticals
Industry
Enrollment
279 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 69 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
Dec 2010 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Feb 2013 (Actual)
Last update posted
Nov 20, 2013

2010 – 2013

United States locations

U.S. sites
54
U.S. states
29
U.S. cities
54
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Mobile Alabama — —
Not listed Phoenix Arizona — —
Not listed Scottsdale Arizona — —
Not listed Tucson Arizona — —
Not listed Malvern Arkansas — —
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Not listed La Mesa California — —
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Not listed Oceanside California — —
Not listed Palm Springs California — —
Not listed Paramount California — —
Not listed Sacramento California — —
Not listed San Jose California — —
Not listed Walnut Creek California — —
Not listed West Covina California — —
Not listed DeLand Florida — —
Not listed Edgewater Florida — —
Not listed Gainesville Florida — —
Not listed Miami Florida — —
Not listed Oldsmar Florida — —
Not listed Sanford Florida — —
Not listed Atlanta Georgia — —
Not listed Honolulu Hawaii — —
Not listed Meridian Idaho — —
Not listed Gurnee Illinois — —
Not listed Brownsburg Indiana — —
Not listed Newton Kansas — —
Not listed Lexington Kentucky — —
Not listed Baltimore Maryland — —
Not listed Springfield Massachusetts — —
Not listed Lansing Michigan — —
Not listed Olive Branch Mississippi — —
Not listed Omaha Nebraska — —
Not listed Albuquerque New Mexico — —
Not listed Charlotte North Carolina — —
Not listed Greensboro North Carolina — —
Not listed Raleigh North Carolina — —
Not listed Salisbury North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Cleveland Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Duncansville Pennsylvania — —
Not listed Greer South Carolina — —
Not listed Rapid City South Dakota — —
Not listed Bristol Tennessee — —
Not listed Dallas Texas — —
Not listed San Antonio Texas — —
Not listed Salt Lake City Utah — —
Not listed Richmond Virginia — —
Not listed Tacoma Washington — —

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 NCT01265264, 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 Nov 20, 2013 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01265264 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →