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Completed Phase 2 Interventional

Tranilast Plus Allopurinol in Patients With Moderate to Severe Gout (TAnGO)

ClinicalTrials.gov ID: NCT01109121

Public ClinicalTrials.gov record NCT01109121. 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 30, 2026, 4:02 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, Parallel Group Study to Evaluate the Safety and Efficacy of Tranilast in Combination With Allopurinol in Patients With Moderate to Severe Gout (TAnGO)

Brief summary

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

This Phase 2 study will be a multicenter, double-blind, randomized, active-comparator study to evaluate the safety and efficacy of tranilast in combination with allopurinol in patients with hyperuricemia and moderate to severe gout.

Study identification

NCT ID
NCT01109121
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Nuon Therapeutics, Inc.
Industry
Enrollment
112 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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
Jun 2010 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Jan 2011 (Actual)
Last update posted
Jan 6, 2011

2010 – 2011

United States locations

U.S. sites
24
U.S. states
20
U.S. cities
24
Facility City State ZIP Site status
Nuon Investigative Site La Jolla California — —
Nuon Investigative Site Santa Maria California — —
Nuon Investigative Site Washington D.C. District of Columbia — —
Nuon Investigative Site New Port Richey Florida — —
Nuon Investigative Site Honolulu Hawaii — —
Nuon Investigative Site Boise Idaho — —
Nuon Investigative Site Bloomington Indiana — —
Nuon Investigative Site Owensboro Kentucky — —
Nuon Investigative Site Baltimore Maryland — —
Nuon Investigative Site Wheaton Maryland — —
Nuon Investigative Site Billings Montana — —
Nuon Investigative Site Omaha Nebraska — —
Nuon Investigative Site Reno Nevada — —
Nuon Investigative Site Teaneck New Jersey — —
Nuon Investigative Site Durham North Carolina — —
Nuon Investigative Site Cincinnati Ohio — —
Nuon Investigative Site Oklahoma City Oklahoma — —
Nuon Investigative Site Lake Oswego Oregon — —
Nuon Investigative Site Duncansville Pennsylvania — —
Nuon Investigative Site West Reading Pennsylvania — —
Nuon Investigative Site Charleston South Carolina — —
Nuon Investigative Site Greenville South Carolina — —
Nuon Investigative Site Waco Texas — —
Nuon Investigative Site Spokane 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 NCT01109121, 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 6, 2011 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01109121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →